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Molecular and Cellular Endocrinology|November 15, 2002
Current approaches for deciphering the molecular basis of combined anterior pituitary hormone deficiency in humansSerge AmselemThe Journal of Clinical Endocrinology and Metabolism|July 7, 2005
Functional relationship between LHX4 and POU1F1 in light of the LHX4 mutation identified in patients with pituitary defectsKalotina Machinis, Serge AmselemOrphanet Journal of Rare Diseases|April 8, 2025
The RaDiCo information system for rare disease cohortsPaul Landais, Sonia Gueguen, Annick Clement, et al.Clinical Endocrinology|April 28, 2011
A novel POU1F1 mutation (p.Thr168IlefsX7) associated with an early and severe form of combined pituitary hormone deficiency: functional analysis and follow-up from infancy to adulthoodYardena Tenenbaum-Rakover, Marie-Laure Sobrier, Serge AmselemPaediatric Respiratory Reviews|June 2, 2015
Biomarkers in Interstitial lung diseasesNadia Nathan, Harriet Corvol, Serge Amselem, et al.Paediatric Respiratory Reviews|May 5, 2009
Ciliary defects and genetics of primary ciliary dyskinesiaEstelle Escudier, Philippe Duquesnoy, Jean François Papon, et al.Orphanet Journal of Rare Diseases|October 30, 2021
RaDiCo, the French national research program on rare disease cohortsSerge Amselem, Sonia Gueguen, Jérôme Weinbach, et al.Anesthesia and Analgesia|January 29, 2002
Screening patients with prolonged neuromuscular blockade after succinylcholine and mivacuriumCharles Cerf, Martine Mesguish, Inanna Gabriel, et al.Arthritis and Rheumatism|March 20, 2013
Familial Mediterranean fever in heterozygotes: are we able to accurately diagnose the disease in very young children?Véronique Hentgen, Gilles Grateau, Katia Stankovic-Stojanovic, et al.Journal of Medical Case Reports|December 31, 2014
Clinical and molecular findings in a Moroccan patient with popliteal pterygium syndrome: a case reportIlham Ratbi, Nawfal Fejjal, Marie Legendre, et al.Pageof 13