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American Journal of Medical Genetics. Part A|April 23, 2017
Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feetMelanie Lacaria, Myriam Srour, Jacques L Michaud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 3, 1999
[Protein requirements in children during states of stress. Committee on Nutrition of the French Society of Pediatrics]B Beaufrère, J L Bresson, A Briend, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 15, 2021
Differential auditory brain response abnormalities in two intellectual disability conditions: SYNGAP1 mutations and Down syndromeValérie Côté, Inga S Knoth, Kristian Agbogba, et al.
Revue Neurologique|March 31, 2000
[Late cerebrovascular complications of cardiac transplantation]B Guillon, S Wiertlewski, J N Trochu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 1996
[Liver transplantation in an adolescent with cystic fibrosis]P Thevenot, F Gottrand, E Tassin, et al.
Preventive Medicine|July 9, 2022
Effectiveness of incentives to improve the reach of health promotion programs- a systematic review and meta-analysisTzeyu L Michaud, Paul A Estabrooks, Wen You, et al.
Human Mutation|April 14, 2015
A Gain-of-Function Mutation in NALCN in a Child with Intellectual Disability, Ataxia, and ArthrogryposisKyota Aoyagi, Elsa Rossignol, Fadi F Hamdan, et al.
Analytical Chemistry|January 31, 2002
Enzymatic decarboxylation of tyrosine and phenylalanine to enhance volatility for high-precision isotopic analysisBassem I Ziadeh, Anthony L Michaud, Nabil M R Saad, et al.
Alimentary Pharmacology & Therapeutics|September 13, 2001
Lansoprazole in children: pharmacokinetics and efficacy in reflux oesophagitisC Faure, L Michaud, E K Shaghaghi, et al.
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