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1مؤتمر
المؤلفون: Dusatkova, Petra, Pfäffle, Roland W., Obermannova, Barbora, Verkauskienė, Rasa, Akulevich, Natallia, Malikova, Jana, Pribilincova, Zuzana, Sallai, Agnes, Stipancic, Gordana, Krzisnik, Ciril, Blum, Werner, Parks, John, Cinek, Ondrej, Lebl, Jan
المصدر: 9th Joint Meeting of Paediatric Endocrinology. Theme: "Predictive Medicine to Improve the Care of Children" : September 19-22, Milan, Italy : Abstract Book / Organising Committee: Franco Chiarelli, Chieti Marco Cappa [et al.] ; ESPE-PES-APEG-APPES-ASPAE-JSPE-SLEP, Milano : European Society for Paediatric Endocrinology (PSPE), 2013, p. 50, no. FC10-179
مصطلحات موضوعية: Pituitary gland, Pathology, Pituitary hormones, Deficiency, Homeodomain proteins, Genetics, Mutation, Europe, info:eu-repo/classification/udc/616.43
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2مؤتمر
المؤلفون: Dusatkova, Petra, Pfäffle, Roland W., Obermannova, Barbora, Verkauskienė, Rasa, Akulevich, Natallia, Malikova, Jana, Pribilincova, Zuzana, Sallai, Agnes, Stipancic, Gordana, Krzisnik, Ciril, Blum, Werner, Parks, John, Cinek, Ondrej, Lebl, Jan
المصدر: 9th Joint Meeting of Paediatric Endocrinology. Theme: "Predictive Medicine to Improve the Care of Children" : September 19-22, Milan, Italy : Abstract Book / Organising Committee: Franco Chiarelli, Chieti Marco Cappa [et al.] ; ESPE-PES-APEG-APPES-ASPAE-JSPE-SLEP, Milano : European Society for Paediatric Endocrinology (PSPE), 2013, p. 50, no. FC10-179
مصطلحات موضوعية: Pituitary gland, Pathology, Pituitary hormones, Deficiency, Homeodomain proteins, Genetics, Mutation, Europe, info:eu-repo/classification/udc/616.43
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3دورية أكاديمية
المؤلفون: Boesgaard, Trine W, Pruhova, Stepanka, Andersson, Ehm A, Cinek, Ondrej, Obermannova, Barbora, Lauenborg, Jeannet, Damm, Peter, Bergholdt, Regine, Pociot, Flemming, Pisinger, Charlotta, Barbetti, Fabrizio, Lebl, Jan, Pedersen, Oluf, Hansen, Torben
المصدر: Boesgaard , T W , Pruhova , S , Andersson , E A , Cinek , O , Obermannova , B , Lauenborg , J , Damm , P , Bergholdt , R , Pociot , F , Pisinger , C , Barbetti , F , Lebl , J , Pedersen , O & Hansen , T 2010 , ' Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY) ' , BMC Medical Genetics , vol. 11 , pp. 42 . https://doi.org/10.1186/1471-2350-11-42Test
مصطلحات موضوعية: Diabetes Mellitus, Type 1, Type 2, Diabetes, Gestational, Female, Genetic Variation, Humans, Insulin, Male, Mutation, Pedigree, Phenotype, Pregnancy, Young Adult
العلاقة: https://portal.findresearcher.sdu.dk/da/publications/cf30b8d0-aa95-11df-b62d-000ea68e967bTest
الإتاحة: https://doi.org/10.1186/1471-2350-11-42Test
https://portal.findresearcher.sdu.dk/da/publications/cf30b8d0-aa95-11df-b62d-000ea68e967bTest -
4دورية أكاديمية
المؤلفون: Boesgaard, Trine W, Pruhova, Stepanka, Andersson, Ehm A, Cinek, Ondrej, Obermannova, Barbora, Lauenborg, Jeannet, Damm, Peter, Bergholdt, Regine, Pociot, Flemming, Pisinger, Charlotta, Barbetti, Fabrizio, Lebl, Jan, Pedersen, Oluf, Hansen, Torben
المصدر: Boesgaard , T W , Pruhova , S , Andersson , E A , Cinek , O , Obermannova , B , Lauenborg , J , Damm , P , Bergholdt , R , Pociot , F , Pisinger , C , Barbetti , F , Lebl , J , Pedersen , O & Hansen , T 2010 , ' Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY) ' , B M C Medical Genetics , vol. 11 , pp. 42 . https://doi.org/10.1186/1471-2350-11-42Test
مصطلحات موضوعية: Diabetes Mellitus, Type 1, Type 2, Diabetes, Gestational, Female, Genetic Variation, Humans, Insulin, Male, Mutation, Pedigree, Phenotype, Pregnancy, Young Adult
الإتاحة: https://doi.org/10.1186/1471-2350-11-42Test
https://curis.ku.dk/portal/da/publications/further-evidence-that-mutations-in-ins-can-be-a-rare-cause-of-maturityonset-diabetes-of-the-young-modyTest(5a4f0ce9-07ef-405f-a8f0-9101fd28372a).html
