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DUK10138432_004
NEWS - Coronavirus: Corona Impfung
THE HAGUE - vaccine against coronavirus COVID-19 coronavirus coronavacccin A doctor vaccinates a patient. Minister Hugo de Jonge, together with Germany, France and Italy, is buying 300 million doses of a British vaccine that has yet to be proven to be effective and safe. Countries and pharmaceutical companies are hastily looking for a drug and vaccine for the corona virus.
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(c) Dukas -
DUK10138432_011
NEWS - Coronavirus: Corona Impfung
THE HAGUE - vaccine against coronavirus COVID-19 coronavirus coronavacccin A doctor vaccinates a patient. Minister Hugo de Jonge, together with Germany, France and Italy, is buying 300 million doses of a British vaccine that has yet to be proven to be effective and safe. Countries and pharmaceutical companies are hastily looking for a drug and vaccine for the corona virus.
*** Local Caption *** 31421955
(c) Dukas -
DUK10138432_010
NEWS - Coronavirus: Corona Impfung
THE HAGUE - vaccine against coronavirus COVID-19 coronavirus coronavacccin A doctor vaccinates a patient. Minister Hugo de Jonge, together with Germany, France and Italy, is buying 300 million doses of a British vaccine that has yet to be proven to be effective and safe. Countries and pharmaceutical companies are hastily looking for a drug and vaccine for the corona virus.
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(c) Dukas -
DUK10111766_043
FEATURE - Pix of the Day: Bilder des Tages
The produce department of a supermarket in New York on Tuesday, January 15, 2019. (ÂPhoto by Richard B. Levine) *** Local Caption *** 25286054
(c) Dukas -
DUK10107120_012
NEWS - Heftige Explosion in Paris
January 12, 2019 - Paris, France - An injured man is seen after the explosion of a bakery on the corner of the streets Saint-Cecile and Rue de Trevise in central Paris on January 12, 2019 (FOTO: DUKAS/ZUMA)
(c) Dukas -
DUK10108112_047
FEATURE - Pix of the Day: Bilder des Tages
A worker checks the shelves in the Dirty Lemon beverage store in New York on Friday, September 14, 2018. Coca-Cola is reported to be in talks to take an investment in Dirty Lemon. The store called "The Drug Store" in the Tribeca neighborhood operates on the honor system where after you make your choice you text the company and they charge your pre-set up account. (Photo by Richard B. Levine) *** Local Caption *** 24655403
(c) Dukas -
DUK10075194_045
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Citlalli grabs the door of the refrigerator before her mother can lock it shut at their home in Mexico City, Mexico on June 1, 2017. Because of Citlalli’s condition, her mother keeps the refrigerator and kitchen under lock and key. Delia Citlalli Pineda Corzo, a 21-year-old Mexican girl, lives with her 42-year-old mother Diana Cristina Corzo Zárate in a two-room apartment in Mexico City. She was diagnosed with Prader-Willi syndrome at age four. At age 15, doctors detected that she had diabetes. Citlalli weighs 106 kilos (233.6 pounds) and stands 150 centimeters (4 feet 11 inches). She has a BMI of 50.5, making her morbidly obese. She also suffers from sleep apnea. Citlalli lacks the faculty of speech and cannot read, but her mother says they have developed their own form of communication. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272667
(c) Dukas -
DUK10075194_022
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Citlalli grabs the door of the refrigerator before her mother can lock it shut at their home in Mexico City, Mexico on June 1, 2017. Because of Citlalli’s condition, her mother keeps the refrigerator and kitchen under lock and key. Delia Citlalli Pineda Corzo, a 21-year-old Mexican girl, lives with her 42-year-old mother Diana Cristina Corzo Zárate in a two-room apartment in Mexico City. She was diagnosed with Prader-Willi syndrome at age four. At age 15, doctors detected that she had diabetes. Citlalli weighs 106 kilos (233.6 pounds) and stands 150 centimeters (4 feet 11 inches). She has a BMI of 50.5, making her morbidly obese. She also suffers from sleep apnea. Citlalli lacks the faculty of speech and cannot read, but her mother says they have developed their own form of communication. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272668
(c) Dukas -
DUK10075194_099
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Citlalli eats the popcorn she had just grabbed from the refrigerator before her mother could lock it shut at their home in Mexico City, Mexico on March 29, 2017.
Because of her condition, her mother keeps their refrigerator and kitchen under lock and key. Delia Citlalli Pineda Corzo, a 21-year-old Mexican girl, lives with her 42-year-old mother Diana Cristina Corzo Zárate in a two-room apartment in Mexico City. She was diagnosed with Prader-Willi syndrome at age four. At age 15, doctors detected that she had diabetes. Citlalli weighs 106 kilos (233.6 pounds) and stands 150 centimeters (4 feet 11 inches). She has a BMI of 50.5, making her morbidly obese. She also suffers from sleep apnea. Citlalli lacks the faculty of speech and cannot read, but her mother says they have developed their own form of communication. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272466
(c) Dukas -
DUK10075194_021
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Citlalli gets upset and clutches a pot of popcorn that she grabbed from the refrigerator before her mother locked it shut at their home in Mexico City, Mexico on March 29, 2017. Because of her condition, her mother keeps the refrigerator and kitchen under lock and key. Delia Citlalli Pineda Corzo, a 21-year-old Mexican girl, lives with her 42-year-old mother Diana Cristina Corzo Zárate in a two-room apartment in Mexico City. She was diagnosed with Prader-Willi syndrome at age four. At age 15, doctors detected that she had diabetes. Citlalli weighs 106 kilos (233.6 pounds) and stands 150 centimeters (4 feet 11 inches). She has a BMI of 50.5, making her morbidly obese. She also suffers from sleep apnea. Citlalli lacks the faculty of speech and cannot read, but her mother says they have developed their own form of communication. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272459
(c) Dukas -
DUK10075194_016
REPORTAGE - Mexiko: Leben mit dem Prader-Willi Syndrome
Citlalli gets upset and clutches a pot of popcorn that she grabbed from the refrigerator before her mother locked it shut at their home in Mexico City, Mexico on March 29, 2017. Because of her condition, her mother keeps the refrigerator and kitchen under lock and key. Delia Citlalli Pineda Corzo, a 21-year-old Mexican girl, lives with her 42-year-old mother Diana Cristina Corzo Zárate in a two-room apartment in Mexico City. She was diagnosed with Prader-Willi syndrome at age four. At age 15, doctors detected that she had diabetes. Citlalli weighs 106 kilos (233.6 pounds) and stands 150 centimeters (4 feet 11 inches). She has a BMI of 50.5, making her morbidly obese. She also suffers from sleep apnea. Citlalli lacks the faculty of speech and cannot read, but her mother says they have developed their own form of communication. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In newborns symptoms include weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to obesity and Type 2 diabetes. There may also be mild to moderate intellectual impairment and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Bénédicte Desrus/Sipa USA) *** Local Caption *** 21272454
(c) Dukas