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Journal of Inherited Metabolic Disease|March 3, 2020
Cardiometabolic risk factor clustering in patients with deficient branched-chain amino acid catabolism: A case-control studySofiya Gancheva, Daria Caspari, Alessandra Bierwagen, et al.European Journal of Pediatrics|April 18, 2021
Consensus statements on the information to deliver after a febrile seizureAnna Loussouarn, Anita Devlin, Thomas Bast, et al.Nature Medicine|March 17, 2015
Characterization of pancreatic NMDA receptors as possible drug targets for diabetes treatmentJan Marquard, Silke Otter, Alena Welters, et al.Arthritis Research & Therapy|April 10, 2024
Anxiety and depression symptoms in adolescents and young adults with juvenile idiopathic arthritis: results of an outpatient screeningFlorian Milatz, Jens Klotsche, Martina Niewerth, et al.Diabetologia|November 1, 2025
Heterogeneity in clinically diagnosed type 1 diabetes: characterising a unique cohort with maintained C-peptide secretion in GhanaWilfred Aniagyei, Osei Sarfo-Kantanka, Sumaya Mohayideen, et al.European Journal of Endocrinology|June 2, 2017
Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinaseSarah M Leiter, Victoria E R Parker, Alena Welters, et al.Orphanet Journal of Rare Diseases|January 12, 2013
Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patientsSarah C Grünert, Stephanie Müllerleile, Linda De Silva, et al.American Journal of Human Genetics|January 31, 2017
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual DisabilityYair Anikster, Tobias B Haack, Thierry Vilboux, et al.Nature Communications|November 30, 2016
Increased DNA methylation variability in type 1 diabetes across three immune effector cell typesDirk S Paul, Andrew E Teschendorff, Mary A N Dang, et al.Pageof 13