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European Journal of Pediatrics|November 9, 2002
Glucagon therapy as a possible cause of erythema necrolyticum migrans in two neonates with persistent hyperinsulinaemic hypoglycaemiaMartin Wald, Karin Lawrenz, Doris Luckner, et al.Pediatric Endocrinology Reviews : PER|January 3, 2018
Spontaneous Growth and Effect of Early Therapy with Calcitriol and Phosphate in X-linked Hypophosphatemic RicketsMichele Cagnoli, Roland Richter, Peter Böhm, et al.Orphanet Journal of Rare Diseases|August 11, 2019
Quality of life of children with achondroplasia and their parents - a German cross-sectional studyStefanie Witt, Beate Kolb, Janika Bloemeke, et al.Medizinische Klinik (Munich, Germany : 1983)|March 26, 2002
[Manifestation of Cushing syndrome and osteoporotic fractures in pregnancy in a patient with Carney complex]Kirsten Reschke, Silke Klose, Klaus Mohnike, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 18, 2015
Therapy monitoring in congenital adrenal hyperplasia by dried blood samplesIsabelle Wieacker, Michael Peter, Katrin Borucki, et al.American Journal of Medical Genetics. Part A|August 29, 2018
Development of body proportions in achondroplasia: Sitting height, leg length, arm span, and foot lengthAndrea Merker, Luitgard Neumeyer, Niels Thomas Hertel, et al.The Journal of Endocrinology|December 14, 2004
Serum MEPE-ASARM-peptides are elevated in X-linked rickets (HYP): implications for phosphaturia and ricketsDoron Bresler, Jan Bruder, Klaus Mohnike, et al.Frontiers in Endocrinology|October 14, 2022
Somatostatin receptors in congenital hyperinsulinism: Biology to bedsideMirjam E van Albada, Klaus Mohnike, Mark J Dunne, et al.Seminars in Pediatric Surgery|December 28, 2010
Glucose metabolism and neurological outcome in congenital hyperinsulinismAnja Ludwig, Katja Ziegenhorn, Susann Empting, et al.Bone|March 18, 2025
Limb lengthening in individuals with achondroplasia: Analysis of an international surveyChristoph Beger, Inês Alves, Patricia Carl-Innig, et al.Pageof 11