نتائج البحث - "W Oostdijk"

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Phenotypic features and response to growth hormone treatment of patients with a molecular defect of the IGF-1 receptor

المؤلفون: Kant Sg, M. Losekoot, Walenkamp Mje, Hokken-Koelega Acs, van Duyvenvoorde Ha, Zandwijken Grj, J.M. Wit, W. Oostdijk, Robers Jml

المصدر: Yearbook of Paediatric Endocrinology.

مصطلحات موضوعية: Growth hormone treatment, medicine.medical_specialty, Endocrinology, Internal medicine, medicine, Biology, Receptor, Phenotype

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::faa39bbcf97de0d74247c606c903371b
https://doi.org/10.1530/ey.16.4.4

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Contents Vol. 81, 2014

المؤلفون: Ghaniya Daar, Julia Kowalczyk, Barbara Wolters, A. Fretzayas, S.G. Kant, Christian L. Roth, Anke Hinney, C. Halsey, Şükrü Hatun, V. Guarnotta, Sibel Kalaça, H. McDevitt, Thomas Reinehr, C. Giordano, A. Papadimitriou, Sümeyye Ercan, D.T. Papadimitriou, A. Papadopoulou, Lou Metherell, Thekla Poukoulidou, D. Haring, Marc Maes, Stine Linding Andersen, A. Ciresi, Satz Mengensatzproduktion, Selim Kurtoglu, Aydin Erdemir, Capan Konca, Yuksel Pehlevan, Aysegul Yuksel, Osman Baştuğ, Zelal Kahramaner, Faruk Hadziselimovic, Şenol Köroğlu, Werner Druck Medien Ag, Sedat Yilmaz, Peter Laurberg, Ferhan Elmali, H.J. van der Kamp, Mehmet Tekin, Abdullah Arpaci, A.C.J. Gijsbers, M.C. Amato, Elif Ozsu, Jean De Schepper, N. El-Fakhri, Ali Yikilmaz, Gül Yeşiltepe Mutlu, W. Oostdijk, S.F. Ahmed, Mehmet Turgut, C. Marakaki, M.G. Shaikh, Mehmet Bülbül, C.A.L. Ruivenkamp, Filiz Mine Çizmecioğlu

المصدر: Hormone Research in Paediatrics. 81:I-VI

مصطلحات موضوعية: Endocrinology, Endocrinology, Diabetes and Metabolism, Pediatrics, Perinatology and Child Health, Botany, Physiology, Biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::5f8e44cb406e0fa138a7b60c63b344fb
https://doi.org/10.1159/000364802

Find this article in full text from ProQuest

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The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients

المساهمون: Endocrinology, Graduate School, Amsterdam Gastroenterology Endocrinology Metabolism, Laboratory for Endocrinology, Amsterdam Neuroscience, Amsterdam Public Health, Human Genetics, Paediatrics, Amsterdam Cardiovascular Sciences, Amsterdam Reproduction & Development (AR&D), Paediatric Endocrinology, Internal Medicine

المصدر: Journal of clinical endocrinology and metabolism, 98(12), 4942-4952. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 98(12), 4942-4952. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 98(12), 4942-4952

مصطلحات موضوعية: Delayed puberty, Adult, Male, medicine.medical_specialty, Aging, Heterozygote, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Immunoglobulins, Context (language use), Biochemistry, Testicular Diseases, Endocrinology, X Chromosome Inactivation, Internal medicine, medicine, Factor V Leiden, Congenital Hypothyroidism, Humans, Child, Aged, 80 and over, Family Health, Metabolic Syndrome, Puberty, Delayed, business.industry, Human Growth Hormone, Biochemistry (medical), Infant, Membrane Proteins, Genetic Diseases, X-Linked, Organ Size, medicine.disease, Congenital hypothyroidism, Hypoprolactinemia, Prolactin, Female, Metabolic syndrome, medicine.symptom, business, Body mass index, Weight gain

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17eb6e22e0801827994fba2a88dfa2d8
https://pure.eur.nl/en/publications/51ed2254-11a0-4202-8c57-63351e3c7191

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IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management

المؤلفون: S D, Joustra, C A, Heinen, N, Schoenmakers, M, Bonomi, B E P B, Ballieux, M-O, Turgeon, D J, Bernard, E, Fliers, A S P, van Trotsenburg, M, Losekoot, L, Persani, J M, Wit, N R, Biermasz, A M, Pereira, W, Oostdijk, N, Zwaveling-Soonawala

المصدر: The Journal of Clinical Endocrinology and Metabolism

مصطلحات موضوعية: Adult, Aged, 80 and over, Male, Adolescent, Immunoglobulins, Infant, Membrane Proteins, Genetic Diseases, X-Linked, Syndrome, Middle Aged, Neuropsychological Tests, Corrections, Thyroxine, Young Adult, Hypothyroidism, Attention Deficit Disorder with Hyperactivity, Child, Preschool, Practice Guidelines as Topic, Quality of Life, Humans, Female, Child, Aged

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::e360e84dc02b1b4709de2f1c4af744e6
https://pubmed.ncbi.nlm.nih.gov/28586455

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Novel Leptin Receptor Mutations Identified in Two Girls with Severe Obesity Are Associated with Increased Bone Mineral Density

المؤلفون: Egbert Bakker, Monique Losekoot, W. Oostdijk, Jan M. Wit, Henriette A. Delemarre-van de Waal, Mieke C Houdijk, Elsa C. Bik, André G. Uitterlinden, Sabine E. Hannema, Sarina G. Kant, Annemieke J.M.H. Verkerk, Arie van Haeringen

المساهمون: Pediatric surgery, Internal Medicine

المصدر: Hannema, S E, Wit, J M, Houdijk, M E C A M, Van Haeringen, A, Bik, E C, Verkerk, A J M H, Uitterlinden, A G, Kant, S G, Oostdijk, W, Bakker, E, Delemarre-Van De Waal, H A & Losekoot, M 2016, ' Novel Leptin Receptor Mutations Identified in Two Girls with Severe Obesity Are Associated with Increased Bone Mineral Density ', Hormone Research in Paediatrics, vol. 85, no. 6, pp. 412-420 . https://doi.org/10.1159/000444055
Hormone Research in Paediatrics, 85(6), 412-420
Hormone Research in Paediatrics, 85(6), 412-420. S. Karger AG
Hormone Research in Paediatrics, 85(6), 412-420. Karger