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DUKAS_167022882_FER
Why some Labrador dogs are prone to obesity
Ferrari Press Agency
Labrador 1
Ref 15645
07/03/2024
See Ferrari text
Pictures must credit: University of Cambridge
A new study into why many Labrador dogs are prone to obesity has discovered it’s down to a genetic mutation
Around a quarter of Labrador retriever dogs face a double-whammy of feeling hungry all the time and burning fewer calories due to this mutation.
This obesity-driving combination means that dog owners must be particularly strict with feeding and exercising their Labradors to keep them slim.
The mutation is in a gene called POMC, which plays a critical role in hunger and energy use.
Around 25% of all Labradors and 66% of flat-coated retriever dogs have the POMC mutation, which researchers previously showed causes increased interest in food and risk of obesity.
The new study reveals how the mutation profoundly changes the way Labrador retrievers behave around food.
It found that although they don’t need to eat more to feel full, they are hungrier in between meals.
In addition, dogs with the POMC mutation were found to use around 25% less energy at rest than dogs without it, meaning they don’t need to consume as many calories to maintain a healthy body weight.
The study was carried out at the University of Cambridge in the UK.
OPS:Three hours after breakfast, this Labrador is offered a sausage in a box by the female researcher - which it can see and smell, but not eat. Dogs with the genetic mutation try significantly harder to get the sausage from the box than dogs without it, indicating greater hunger.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_167022881_FER
Why some Labrador dogs are prone to obesity
Ferrari Press Agency
Labrador 1
Ref 15645
07/03/2024
See Ferrari text
Pictures must credit: University of Cambridge
A new study into why many Labrador dogs are prone to obesity has discovered it’s down to a genetic mutation
Around a quarter of Labrador retriever dogs face a double-whammy of feeling hungry all the time and burning fewer calories due to this mutation.
This obesity-driving combination means that dog owners must be particularly strict with feeding and exercising their Labradors to keep them slim.
The mutation is in a gene called POMC, which plays a critical role in hunger and energy use.
Around 25% of all Labradors and 66% of flat-coated retriever dogs have the POMC mutation, which researchers previously showed causes increased interest in food and risk of obesity.
The new study reveals how the mutation profoundly changes the way Labrador retrievers behave around food.
It found that although they don’t need to eat more to feel full, they are hungrier in between meals.
In addition, dogs with the POMC mutation were found to use around 25% less energy at rest than dogs without it, meaning they don’t need to consume as many calories to maintain a healthy body weight.
The study was carried out at the University of Cambridge in the UK.
OPS:Three hours after breakfast, this Labrador is offered a sausage in a box by the female researcher - which it can see and smell, but not eat. Dogs with the genetic mutation try significantly harder to get the sausage from the box than dogs without it, indicating greater hunger.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_167022879_FER
Why some Labrador dogs are prone to obesity
Ferrari Press Agency
Labrador 1
Ref 15645
07/03/2024
See Ferrari text
Pictures must credit: University of Cambridge
A new study into why many Labrador dogs are prone to obesity has discovered it’s down to a genetic mutation
Around a quarter of Labrador retriever dogs face a double-whammy of feeling hungry all the time and burning fewer calories due to this mutation.
This obesity-driving combination means that dog owners must be particularly strict with feeding and exercising their Labradors to keep them slim.
The mutation is in a gene called POMC, which plays a critical role in hunger and energy use.
Around 25% of all Labradors and 66% of flat-coated retriever dogs have the POMC mutation, which researchers previously showed causes increased interest in food and risk of obesity.
The new study reveals how the mutation profoundly changes the way Labrador retrievers behave around food.
It found that although they don’t need to eat more to feel full, they are hungrier in between meals.
In addition, dogs with the POMC mutation were found to use around 25% less energy at rest than dogs without it, meaning they don’t need to consume as many calories to maintain a healthy body weight.
The study was carried out at the University of Cambridge in the UK.
OPS:All Labradors and flatcoated retrievers are highly food-motivated. But dogs with the genetic mutation face a double whammy: they not only want to eat more, but also need fewer calories because they’re not burning them off as fast.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_167022877_FER
Why some Labrador dogs are prone to obesity
Ferrari Press Agency
Labrador 1
Ref 15645
07/03/2024
See Ferrari text
Pictures must credit: University of Cambridge
A new study into why many Labrador dogs are prone to obesity has discovered it’s down to a genetic mutation
Around a quarter of Labrador retriever dogs face a double-whammy of feeling hungry all the time and burning fewer calories due to this mutation.
This obesity-driving combination means that dog owners must be particularly strict with feeding and exercising their Labradors to keep them slim.
The mutation is in a gene called POMC, which plays a critical role in hunger and energy use.
Around 25% of all Labradors and 66% of flat-coated retriever dogs have the POMC mutation, which researchers previously showed causes increased interest in food and risk of obesity.
The new study reveals how the mutation profoundly changes the way Labrador retrievers behave around food.
It found that although they don’t need to eat more to feel full, they are hungrier in between meals.
In addition, dogs with the POMC mutation were found to use around 25% less energy at rest than dogs without it, meaning they don’t need to consume as many calories to maintain a healthy body weight.
The study was carried out at the University of Cambridge in the UK.
OPS:Three hours after breakfast, this Labrador is offered a sausage in a box by the female researcher - which it can see and smell, but not eat. Dogs with the genetic mutation try significantly harder to get the sausage from the box than dogs without it, indicating greater hunger.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_167022872_FER
Why some Labrador dogs are prone to obesity
Ferrari Press Agency
Labrador 1
Ref 15645
07/03/2024
See Ferrari text
Pictures must credit: University of Cambridge
A new study into why many Labrador dogs are prone to obesity has discovered it’s down to a genetic mutation
Around a quarter of Labrador retriever dogs face a double-whammy of feeling hungry all the time and burning fewer calories due to this mutation.
This obesity-driving combination means that dog owners must be particularly strict with feeding and exercising their Labradors to keep them slim.
The mutation is in a gene called POMC, which plays a critical role in hunger and energy use.
Around 25% of all Labradors and 66% of flat-coated retriever dogs have the POMC mutation, which researchers previously showed causes increased interest in food and risk of obesity.
The new study reveals how the mutation profoundly changes the way Labrador retrievers behave around food.
It found that although they don’t need to eat more to feel full, they are hungrier in between meals.
In addition, dogs with the POMC mutation were found to use around 25% less energy at rest than dogs without it, meaning they don’t need to consume as many calories to maintain a healthy body weight.
The study was carried out at the University of Cambridge in the UK.
OPS:Three hours after breakfast, this Labrador is offered a sausage in a box by the female researcher - which it can see and smell, but not eat. Dogs with the genetic mutation try significantly harder to get the sausage from the box than dogs without it, indicating greater hunger.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_167022871_FER
Why some Labrador dogs are prone to obesity
Ferrari Press Agency
Labrador 1
Ref 15645
07/03/2024
See Ferrari text
Pictures must credit: University of Cambridge
A new study into why many Labrador dogs are prone to obesity has discovered it’s down to a genetic mutation
Around a quarter of Labrador retriever dogs face a double-whammy of feeling hungry all the time and burning fewer calories due to this mutation.
This obesity-driving combination means that dog owners must be particularly strict with feeding and exercising their Labradors to keep them slim.
The mutation is in a gene called POMC, which plays a critical role in hunger and energy use.
Around 25% of all Labradors and 66% of flat-coated retriever dogs have the POMC mutation, which researchers previously showed causes increased interest in food and risk of obesity.
The new study reveals how the mutation profoundly changes the way Labrador retrievers behave around food.
It found that although they don’t need to eat more to feel full, they are hungrier in between meals.
In addition, dogs with the POMC mutation were found to use around 25% less energy at rest than dogs without it, meaning they don’t need to consume as many calories to maintain a healthy body weight.
The study was carried out at the University of Cambridge in the UK.
OPS:All Labradors and flatcoated retrievers are highly food-motivated. But dogs with the genetic mutation face a double whammy: they not only want to eat more, but also need fewer calories because they’re not burning them off as fast.
Picture supplied by Ferrari
(FOTO: DUKAS/FERRARI PRESS) -
DUKAS_160969588_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969590_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969589_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969586_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969582_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969587_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969581_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969573_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969579_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969574_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969575_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969572_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969576_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUKAS_160969591_EYE
Covid hunters: the amateur sleuths tracking the virus and its variants. Ryan Hisner
How a schoolteacher and a dog educator became crucial to the global fight against coronavirus.
At the onset of the Covid-19 pandemic, countries would receive daily updates collated from data that had been analysed by the world-leading virologists and academics.
But three years later, the pandemic's trajectory is becoming more difficult to predict - and decision-makers are increasingly reliant on the warnings of a diverse bunch of independent researchers.
Ryan Hisner, a teacher from Indiana, US, was listed alongside various academic co-authors on a paper in Nature, describing how the antiviral drug molnupiravir used to treat patients with Covid-19 may be fuelling the evolution of new variants by creating a specific set of mutations.
Ryan Hisner, 39, schoolteacher in Monroe, Indiana.
© Anna Powell Denton / Guardian / eyevine
Contact eyevine for more information about using this image:
T: +44 (0) 20 8709 8709
E: info@eyevine.com
http://www.eyevine.com (FOTO: DUKAS/EYEVINE)
© Guardian / eyevine. All Rights Reserved. -
DUK10153242_013
NEWS - Coronavirus: Illustration von Corona-Varianten
Entstehung einer Corona-Variante, Symbolfoto / action press *** Local Caption *** 40896044
(c) Dukas -
DUK10153242_012
NEWS - Coronavirus: Illustration von Corona-Varianten
Entstehung einer Corona-Variante, Symbolfoto / action press *** Local Caption *** 40896045
(c) Dukas -
DUK10153242_011
NEWS - Coronavirus: Illustration von Corona-Varianten
Neue Corona-Variante XBB.1.5, Symbolfoto / action press *** Local Caption *** 40896041
(c) Dukas -
DUK10153242_010
NEWS - Coronavirus: Illustration von Corona-Varianten
Neue Corona-Variante XBB.1.5, Symbolfoto / action press *** Local Caption *** 40896042
(c) Dukas -
DUK10153242_009
NEWS - Coronavirus: Illustration von Corona-Varianten
Entstehung einer Corona-Variante, Symbolfoto / action press *** Local Caption *** 40896047
(c) Dukas -
DUK10153242_008
NEWS - Coronavirus: Illustration von Corona-Varianten
Corona-Variante XBB.1.5, Symbolfoto / action press *** Local Caption *** 40896043
(c) Dukas -
DUK10153242_007
NEWS - Coronavirus: Illustration von Corona-Varianten
Entstehung einer Corona-Variante, Symbolfoto / action press *** Local Caption *** 40896046
(c) Dukas -
DUK10153242_006
NEWS - Coronavirus: Illustration von Corona-Varianten
Neue Corona-Variante, Symbolfoto / action press *** Local Caption *** 40898980
(c) Dukas -
DUK10153242_005
NEWS - Coronavirus: Illustration von Corona-Varianten
Corona-Variante BF.7, Symbolfoto / action press *** Local Caption *** 40898985
(c) Dukas -
DUK10153242_004
NEWS - Coronavirus: Illustration von Corona-Varianten
Corona-Variante BF.7, Symbolfoto / action press *** Local Caption *** 40898981
(c) Dukas -
DUK10153242_003
NEWS - Coronavirus: Illustration von Corona-Varianten
Corona-Variante XBB.1.5, Symbolfoto / action press *** Local Caption *** 40898983
(c) Dukas -
DUK10153242_002
NEWS - Coronavirus: Illustration von Corona-Varianten
Neue Corona-Variante, Symbolfoto / action press *** Local Caption *** 40898982
(c) Dukas -
DUK10153242_001
NEWS - Coronavirus: Illustration von Corona-Varianten
Corona-Variante XBB.1.5, Symbolfoto / action press *** Local Caption *** 40898984
(c) Dukas -
DUK10148733_014
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla in 2020 (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest milestones. If she goes to a new toy that she was nervous about, *
(c) Dukas -
DUK10148733_001
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla during occupational therapy in 2018 (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest milestones. If she goes to a new toy *
(c) Dukas -
DUK10148733_017
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla at speech therapy in 2019 (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest milestones. If she goes to a new toy that she *
(c) Dukas -
DUK10148733_006
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla at occupational therapy in 2018 (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest milestones. If she goes to a new toy tha *
(c) Dukas -
DUK10148733_018
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla and Dallis together in 2021 (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest milestones. If she goes to a new toy that sh *
(c) Dukas -
DUK10148733_009
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla in 2019 was diagnosed with NFIX gene mutation and the BPTF gene mutation (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest *
(c) Dukas -
DUK10148733_015
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla, pictured here in 2018, is the only person in the world with two genetic mutations (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even th *
(c) Dukas -
DUK10148733_003
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla, pictured her in 2015, could not sit up or roll over and did not smile until she was around a year old (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: " *
(c) Dukas -
DUK10148733_008
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla in 2015 (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest milestones. If she goes to a new toy that she was nervous about, *
(c) Dukas -
DUK10148733_019
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Hannah and Layla in 2018 (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest milestones. If she goes to a new toy that she was ner *
(c) Dukas -
DUK10148733_016
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla in 2015 (Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest milestones. If she goes to a new toy that she was nervous about, *
(c) Dukas -
DUK10148733_005
SCHICKSALE - Lebenserwartung unbekannt: Layla Wood ist der einzige Mensch auf der Welt mit zwei genetischen Mutationen
Layla with her siblings, Wyatt and Samantha in 2018(Collect/PA Real Life). *** Mum whose daughter is only person with two genetic mutations making her life expectancy unknown says she is "happiest girl on the planet"
By Joe Pagnelli, PA Real Life
A mum claims her daughter is the "happiest girl on the planet" despite living under a huge question mark as the seven-year-old is the only person in the world with two genetic mutations which mean no one knows her life expectancy.
It took more than a year of her missing "every milestone" before Hannah Wood, 27, says her daughter Layla's condition really started to worry doctors.
In November 2018, she was finally diagnosed with the NFIX gene mutation, which causes developmental and intellectual delay, epilepsy, overgrowth, skeletal anomalies and vision impairment. But she was also diagnosed with the BPTF gene mutation, which is linked to breathing issues, heart problems and childhood cancer, for which she is tested every year.
Yet Hannah, who lives in Ocala, Florida, USA, with Layla, and her partner Dallis Crossin, 28, with whom she runs a handyman business, and her other children Samantha, nine, Wyatt, eight, and three-month-old Arabella, said: "She has such a positive light about her.
"Anyone who knows Layla knows she is a star.
"She’s the happiest girl in the world. Everything makes her happy, she brightens everyone’s day."
Layla's genetic mutations mean she cannot speak or eat on her own. Despite being seven, she still has to wear a nappy and needs 24-hour supervision.
She said: "I would never trade her for anything.
"Because we don’t know what the future holds, we just take it day by day and make the most of our time with her.
"But I still allow myself to dream of her growing older."
When Layla does hit a milestone - such as learning to walk on her own in the last year - it is a cause for celebration.
Hannah said: "We celebrate even the smallest milestones. If she goes to *
(c) Dukas -
DUK10148602_011
NEWS - Coronavirus: München - Shopping in der Innenstadt trotz steigender Coronazahlen
Während die Covid-19 Ansteckungen in Bayern neue Negativrekorde erreichen, gehen am 15.3.2022 in München zahlreiche Menschen shoppen. - While the coronavirus infections reach new highs people go shopping in the Munich pedestrian zone on March 15, 2022. / 150622 *** Local Caption *** 38351357
(c) Dukas -
DUK10148602_010
NEWS - Coronavirus: München - Shopping in der Innenstadt trotz steigender Coronazahlen
Tchibo Filiale. Während die Covid-19 Ansteckungen in Bayern neue Negativrekorde erreichen, gehen am 15.3.2022 in München zahlreiche Menschen shoppen. - Tchibo branch. While the coronavirus infections reach new highs people go shopping in the Munich pedestrian zone on March 15, 2022. / 150622 *** Local Caption *** 38351370
(c) Dukas -
DUK10148602_009
NEWS - Coronavirus: München - Shopping in der Innenstadt trotz steigender Coronazahlen
Während die Covid-19 Ansteckungen in Bayern neue Negativrekorde erreichen, gehen am 15.3.2022 in München zahlreiche Menschen shoppen. - While the coronavirus infections reach new highs people go shopping in the Munich pedestrian zone on March 15, 2022. / 150622 *** Local Caption *** 38351353
(c) Dukas -
DUK10148602_008
NEWS - Coronavirus: München - Shopping in der Innenstadt trotz steigender Coronazahlen
Während die Covid-19 Ansteckungen in Bayern neue Negativrekorde erreichen, gehen am 15.3.2022 in München zahlreiche Menschen shoppen. - While the coronavirus infections reach new highs people go shopping in the Munich pedestrian zone on March 15, 2022. / 150622 *** Local Caption *** 38351355
(c) Dukas -
DUK10148602_007
NEWS - Coronavirus: München - Shopping in der Innenstadt trotz steigender Coronazahlen
The North Face Filiale. Während die Covid-19 Ansteckungen in Bayern neue Negativrekorde erreichen, gehen am 15.3.2022 in München zahlreiche Menschen shoppen. - The North Face branch. While the coronavirus infections reach new highs people go shopping in the Munich pedestrian zone on March 15, 2022. / 150622 *** Local Caption *** 38351362
(c) Dukas -
