Showing results (11-20 of 60) with videos related to
Sort By:
Pageof 6
Revue Medicale De Liege|August 16, 2012
[Genetics and environment in chronic inflammatory bowel diseases]E Louis, C Van Kemseke, P Latour, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 13, 2000
[Hereditary neuropathy with tendency to pressure palsies (HNPP) in a child: clinical and biological diagnosis. A case report]G Lesca, S Meunier, A Zine, et al.Scandinavian Journal of Gastroenterology|January 28, 2016
Long-term evolution and predictive factors of mild inflammatory bowel diseaseC Reenaers, C Pirard, C Vankemseke, et al.Acta Gastro-Enterologica Belgica|October 2, 2021
Unusual intra-rectal "laterally spreading tumour" in immunosuppressed patient with ulcerative colitisS Vieujean, P Latour, C Coimbra, et al.Neuromuscular Disorders : NMD|June 16, 2005
A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsiesH Zéphir, T Stojkovic, P Latour, et al.Annals of Tropical Medicine and Parasitology|June 14, 2003
Failure of an ointment based on IR3535 (ethyl butylacetylaminopropionate) to prevent an outbreak of cercarial dermatitis during swimming races across Lake Annecy, FranceE Caumes, S Felder-Moinet, C Couzigou, et al.Neuropediatrics|November 11, 2008
Clinical, electrophysiological and genetic studies of two families with mutations in the GDAP1 geneC Rougeot, S Chabrier, J-P Camdessanche, et al.Diabete & Metabolisme|July 1, 1991
[Insulin secretion in nondiabetic manioc consumers]H Andrianasolo, M C Fleury-Goyon, A Charrie, et al.Revue Neurologique|March 6, 2012
[Non-fortuitous dynamin II mutation-related association: neutropenia and Charcot-Marie-Tooth disease]A Saint-Lézer, G Solé, E Ribeiro, et al.Revue Neurologique|December 17, 2004
[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy]B Degos, A Echaniz-Laguna, P Latour, et al.Pageof 6