يعرض 51 - 57 نتائج من 57 نتيجة بحث عن '"Obermannova, Barbora"', وقت الاستعلام: 0.86s تنقيح النتائج
  1. 51
    دورية أكاديمية
    Treated Autoimmune Thyroid Disease Is Associated with a Decreased Quality of Life among Young Persons with Type 1 Diabetes.

    المؤلفون: Spirkova, Alena, Dusatkova, Petra, Peckova, Monika, Kolouskova, Stanislava, Snajderova, Marta, Obermannova, Barbora, Stechova, Katerina, Hrachovinova, Tamara, Mares, Jiri, Cinek, Ondrej, Lebl, Jan, Sumnik, Zdenek, Pruhova, Stepanka

    المصدر: International Journal of Endocrinology; 5/18/2015, Vol. 2015, p1-9, 9p

    مصطلحات موضوعية: AUTOIMMUNE disease treatment, THYROID diseases, QUALITY of life, TYPE 1 diabetes, IMMUNOPATHOLOGY

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  2. 52
    دورية
    High Incidence of Heterozygous ABCC8and HNF1AMutations in Czech Patients With Congenital Hyperinsulinism

    المؤلفون: Rozenkova, Klara, Malikova, Jana, Nessa, Azizun, Dusatkova, Lenka, Bjørkhaug, Lise, Obermannova, Barbora, Dusatkova, Petra, Kytnarova, Jitka, Aukrust, Ingvild, Najmi, Laeya A., Rypackova, Blanka, Sumnik, Zdenek, Lebl, Jan, Njølstad, Pål R., Hussain, Khalid, Pruhova, Stepanka

    المصدر: The Journal of Clinical Endocrinology & Metabolism; December 2015, Vol. 100 Issue: 12 pE1540-E1549, 10p

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  3. 53
    دورية أكاديمية
    Low-Carbohydrate Diet among Children with Type 1 Diabetes: A Multi-Center Study.

    المؤلفون: Neuman, Vit, Plachy, Lukas, Pruhova, Stepanka, Kolouskova, Stanislava, Petruzelkova, Lenka, Obermannova, Barbora, Vyzralkova, Jana, Konecna, Petra, Vosahlo, Jan, Romanova, Martina, Pavlikova, Marketa, Sumnik, Zdenek

    المصدر: Nutrients; Nov2021, Vol. 13 Issue 11, p3903, 1p

    النص الكامل

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  4. 54
    دورية أكاديمية
    Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).

    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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  5. 55
    دورية أكاديمية
    Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene.

    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


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  6. 56
    دورية
    HNF1Amutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes

    المؤلفون: Dusatkova, Petra, Pruhova, Stepanka, Sumnik, Zdenek, Kolouskova, Stanislava, Obermannova, Barbora, Cinek, Ondrej, Lebl, Jan

    المصدر: Journal of Pediatric Endocrinology & Metabolism; April 2011, Vol. 24 Issue: 3-4 p187-189, 3p


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  7. 57
    دورية أكاديمية
    1378-P: Gluten-Free Diet in Children with Recent-Onset Type 1 Diabetes without Coeliac Disease: A 12-Month Intervention Trial.

    المؤلفون: NEUMAN, VÍT, PRUHOVA, STEPANKA, KULICH, MICHAL, KOLOUŠKOVÁ, STANISLAVA, VOSAHLO, JAN, ROMANOVA, MARTINA, PETRUZELKOVA, LENKA, OBERMANNOVA, BARBORA, CINEK, ONDREJ, SUMNIK, ZDENEK

    المصدر: Diabetes; 2019 Supplement, Vol. 68, pN.PAG-N.PAG, 1p

    النص الكامل

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