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A Gelot

Showing results (61-70 of 69) with videos related to

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Acta Neuropathologica|May 20, 1999
Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two casesD Rodriguez, A Gelot, B della Gaspera, et al.
Digestive Diseases and Sciences|July 1, 1996
Crohn's disease and vitamin B12 metabolismD Lambert, S Benhayoun, C Adjalla, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 2, 2010
[Impact of prenatal corpus callosum agenesis diagnosis on pregnancy outcome. Evaluation of 155 cases between 2000 and 2006]A Isapof, V Kieffer, S Sacco, et al.
Neurology|July 25, 2007
Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated familiesS Passemard, A Gelot, A Fogli, et al.
Neurogastroenterology and Motility|May 20, 2016
Colonic overexpression of the T-type calcium channel Ca<sub>v</sub> 3.2 in a mouse model of visceral hypersensitivity and in irritable bowel syndrome patientsJ Scanzi, A Accarie, E Muller, et al.
Scientific Reports|January 19, 2016
Anti-nociceptive effect of Faecalibacterium prausnitzii in non-inflammatory IBS-like modelsS Miquel, R Martín, A Lashermes, et al.
Cell|March 7, 1998
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndromeV des Portes, J M Pinard, P Billuart, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
Perinatal-lethal Gaucher diseaseC Mignot, A Gelot, B Bessières, et al.
American Journal of Human Genetics|September 22, 2001
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlationD Rodriguez, F Gauthier, E Bertini, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
Acta Neuropathologica|May 20, 1999
Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two casesD Rodriguez, A Gelot, B della Gaspera, et al.
Digestive Diseases and Sciences|July 1, 1996
Crohn's disease and vitamin B12 metabolismD Lambert, S Benhayoun, C Adjalla, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 2, 2010
[Impact of prenatal corpus callosum agenesis diagnosis on pregnancy outcome. Evaluation of 155 cases between 2000 and 2006]A Isapof, V Kieffer, S Sacco, et al.
Neurology|July 25, 2007
Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated familiesS Passemard, A Gelot, A Fogli, et al.
Neurogastroenterology and Motility|May 20, 2016
Colonic overexpression of the T-type calcium channel Ca<sub>v</sub> 3.2 in a mouse model of visceral hypersensitivity and in irritable bowel syndrome patientsJ Scanzi, A Accarie, E Muller, et al.
Scientific Reports|January 19, 2016
Anti-nociceptive effect of Faecalibacterium prausnitzii in non-inflammatory IBS-like modelsS Miquel, R Martín, A Lashermes, et al.
Cell|March 7, 1998
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndromeV des Portes, J M Pinard, P Billuart, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
Perinatal-lethal Gaucher diseaseC Mignot, A Gelot, B Bessières, et al.
American Journal of Human Genetics|September 22, 2001
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlationD Rodriguez, F Gauthier, E Bertini, et al.
Pageof 7