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Frontiers in Microbiology|November 15, 2021
Characterization of the Oral Microbiome Among Children With Type 1 Diabetes Compared With Healthy ChildrenMoti Moskovitz, Mira Nassar, Nadav Moriel, et al.Plos Genetics|July 9, 2019
Analysis of the genetic basis of height in large Jewish nuclear familiesDanny Zeevi, Joshua S Bloom, Meru J Sadhu, et al.Pediatric Endocrinology Reviews : PER|August 12, 2020
A Unique Presentation of XY Gonadal Dysgenesis in Frasier Syndrome due to WT1 Mutation and a Literature ReviewEran Lavi, Mahmud Zighan, Abdulsalam Abu Libdeh, et al.The Journal of Clinical Endocrinology and Metabolism|November 6, 2023
Dasiglucagon for the Treatment of Congenital Hyperinsulinism: A Randomized Phase 3 Trial in Infants and ChildrenPaul S Thornton, Diva D De Leon, Susann Empting, et al.Journal of the Endocrine Society|January 24, 2025
A Novel Homozygous BMP15 Mutation Causes Ovarian Dysgenesis and Primary AmenorrheaAmitay Cohen, Raffaella Rossetti, Natan Florsheim, et al.The Journal of Clinical Endocrinology and Metabolism|August 21, 2020
NKX2-2 Mutation Causes Congenital Diabetes and Infantile Obesity With Paradoxical Glucose-Induced Ghrelin SecretionAdi Auerbach, Amitay Cohen, Noa Ofek Shlomai, et al.European Journal of Endocrinology|September 23, 2023
Loss of function of FIGNL1, a DNA damage response gene, causes human ovarian dysgenesisNatan Florsheim, Larisa Naugolni, Fouad Zahdeh, et al.Journal of Medical Genetics|June 14, 2015
Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stressAriella Weinberg-Shukron, Abdulsalam Abu-Libdeh, Fouad Zhadeh, et al.Plos One|October 2, 2014
A novel familial mutation in the PCSK1 gene that alters the oxyanion hole residue of proprotein convertase 1/3 and impairs its enzymatic activityMichael Wilschanski, Montaser Abbasi, Elias Blanco, et al.American Journal of Medical Genetics. Part A|January 13, 2021
Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneityYaniv Faingelernt, Eli Hershkovitz, Bassam Abu-Libdeh, et al.Pageof 4