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Primary Care Diabetes|January 25, 2023
Effects of a digital diabetes prevention program on cardiovascular risk among individuals with prediabetesTzeyu L Michaud, Fabio A Almeida, Gwenndolyn C Porter, et al.Clinical Genetics|April 28, 2018
Refining the phenotype associated with biallelic DNAJC21 mutationsG D'Amours, F Lopes, J Gauthier, et al.Gastroenterologie Clinique Et Biologique|January 3, 2009
Prevention of relapse by mesalazine (Pentasa) in pediatric Crohn's disease: a multicenter, double-blind, randomized, placebo-controlled trialJ-P Cezard, A Munck, O Mouterde, et al.Human Mutation|June 18, 2011
Mutations in NOTCH2 in families with Hajdu-Cheney syndromeJacek Majewski, Jeremy A Schwartzentruber, Aurore Caqueret, et al.Human Mutation|October 4, 2012
Identification and biochemical characterization of a novel mutation in DDX11 causing Warsaw breakage syndromeJosé-Mario Capo-Chichi, Sanjay Kumar Bharti, Joshua A Sommers, et al.Journal of Medical Genetics|March 26, 2015
Loss-of-function de novo mutations play an important role in severe human neural tube defectsPhilippe Lemay, Marie-Claude Guyot, Élizabeth Tremblay, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 11, 2021
The role of nutrition in non-alcoholic fatty liver disease treatment in obese childrenD Guimber, D Debray, A Bocquet, et al.American Journal of Men'S Health|May 13, 2022
Stress Correlates Related to Depressive Symptoms Among Young Black Men in Southern CaliforniaKeyonna M King, Markisha Key-Hagan, Avni Desai, et al.European Journal of Human Genetics : EJHG|November 20, 2014
A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndromeJulie Gauthier, Bouchra Ouled Amar Bencheikh, Fadi F Hamdan, et al.British Journal of Pharmacology|December 1, 1998
Genotypic and phenotypic analysis of the polymorphic thiopurine S-methyltransferase gene (TPMT) in a European populationC Spire-Vayron de la Moureyre, H Debuysere, B Mastain, et al.Pageof 50