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1دورية أكاديمية
المؤلفون: Obermannova, Barbora1, Pfaeffle, Roland2, Zygmunt-Gorska, Agata3, Starzyk, Jerzy3, Verkauskiene, Rasa4, Smetanina, Natalija4, Bezlepkina, Olga5, Peterkova, Valentina5, Frisch, Herwig6, Cinek, Ondrej1, Child, Christopher J.7, Blum, Werner F.8, Lebl, Jan1
المصدر: Hormone Research in Paediatrics. Nov2011, Vol. 76 Issue 5, p348-354. 7p. 4 Charts, 2 Graphs.
مصطلحات موضوعية: *GENETIC mutation, *MAGNETIC resonance imaging, *PITUITARY gland, *PHENOTYPES, *PITUITARY hormones, *TRANSCRIPTION factors, *CELL lines, *MOLECULAR genetics
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2دورية 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: BMC Medical Genetics; 2010, Vol. 11, p42-45, 4p, 1 Diagram, 1 Chart
مصطلحات موضوعية: GENETIC mutation, INSULIN, GENES, DIAGNOSIS of diabetes, DIABETES in children
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3دورية أكاديمية
المؤلفون: Obermannova, Barbora1,2 obermannova@seznam.cz, Banghova, Karolina1, Sumník, Zdenek1, Dvorakova, Hana M.3, Betka, Jan4, Fencl, Filip1, Kolouskova, Stanislava1, Cinek, Ondrej1, Lebl, Jan1, Sumník, Zdenek (AUTHOR)
المصدر: European Journal of Pediatrics. May2009, Vol. 168 Issue 5, p569-573. 5p. 1 Black and White Photograph.
مصطلحات موضوعية: *HYPERPARATHYROIDISM, *NEONATOLOGY, *NEWBORN infants, *GENETIC mutation, *GENES, *CEREBRAL atrophy, *ADRENALECTOMY, *CALCIUM-binding proteins, *COMPARATIVE studies, *HYPERCALCEMIA, *RESEARCH methodology, *MEDICAL cooperation, *PRENATAL diagnosis, *RESEARCH, *PHENOTYPES, *VITAMIN D deficiency, *EVALUATION research, *SEVERITY of illness index, *GENETIC carriers, *DISEASE complications, *DIAGNOSIS