| dbo:abstract |
هورست بيكل (بالألمانية: Horst Bickel) (و. 1918 – 2000 م) هو طبيب ألماني، ولد في هامبورغ، كان عضوًا في الأكاديمية الألمانية للعلوم ليوبولدينا، توفي عن عمر يناهز 82 عاماً. (ar) Prof. Horst Bickel (* 28. Juni 1918 in Hamburg; † 1. Dezember 2000 in Baabe (Rügen)) war ein deutscher Kinderarzt. (de) Horst Bickel (28 June 1918 – 1 December 2000) was a German medical doctor. With Guido Fanconi, he characterized Glycogen storage disease type XI in 1949. He was also involved in the development of treatments for phenylketonuria. In 1951, Bickel, Evelyn Hickmans and John Gerrard were persuaded by a persistent mother to help her daughter, Sheila, who was suffering from phenylketonuria. They created a diet that was low in phenylalanine and the daughter's condition improved. Bickel, Gerrard and Hickmans were awarded the John Scott Medal in 1962 for their discovery. His birthday, June 28th, which he shares with Robert Guthrie, another important person for Phenylketonuria was taken up by the European Society for Phenylketonuria and Allied Disorders Treated as Phenylketonuria to launch the International PKU Day. (en) Horst Bickel (ur. 18 czerwca 1918 w Hamburgu, zm. 1 grudnia 2000 w Baabe) – niemiecki lekarz. Jako pierwszy na świecie (razem z Guido Fanconim) opisał rzadkie, genetycznie uwarunkowane zaburzenie metaboliczne, nazwane na jego cześć zespołem Fanconiego-Bickela. (pl) |
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هورست بيكل (بالألمانية: Horst Bickel) (و. 1918 – 2000 م) هو طبيب ألماني، ولد في هامبورغ، كان عضوًا في الأكاديمية الألمانية للعلوم ليوبولدينا، توفي عن عمر يناهز 82 عاماً. (ar) Prof. Horst Bickel (* 28. Juni 1918 in Hamburg; † 1. Dezember 2000 in Baabe (Rügen)) war ein deutscher Kinderarzt. (de) Horst Bickel (ur. 18 czerwca 1918 w Hamburgu, zm. 1 grudnia 2000 w Baabe) – niemiecki lekarz. Jako pierwszy na świecie (razem z Guido Fanconim) opisał rzadkie, genetycznie uwarunkowane zaburzenie metaboliczne, nazwane na jego cześć zespołem Fanconiego-Bickela. (pl) Horst Bickel (28 June 1918 – 1 December 2000) was a German medical doctor. With Guido Fanconi, he characterized Glycogen storage disease type XI in 1949. He was also involved in the development of treatments for phenylketonuria. In 1951, Bickel, Evelyn Hickmans and John Gerrard were persuaded by a persistent mother to help her daughter, Sheila, who was suffering from phenylketonuria. They created a diet that was low in phenylalanine and the daughter's condition improved. Bickel, Gerrard and Hickmans were awarded the John Scott Medal in 1962 for their discovery. (en) |
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