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F Leturcq

Showing results (41-50 of 50) with videos related to

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Clinical Genetics|January 6, 2011
Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?M Krahn, M Goicoechea, F Hanisch, et al.
Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Neuropathology and Applied Neurobiology|April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathyM Cerino, E Campana-Salort, A Salvi, et al.
Neurology|May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.
Annals of Neurology|August 1, 1997
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in TurkeyP Dinçer, F Leturcq, I Richard, et al.
Diabetes Care|July 8, 1998
Factors associated with glycemic control. A cross-sectional nationwide study in 2,579 French children with type 1 diabetes. The French Pediatric Diabetes GroupM Rosilio, J B Cotton, M C Wieliczko, et al.
European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Brain : a Journal of Neurology|February 4, 2005
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 geneA Sáenz, F Leturcq, A M Cobo, et al.
Muscle & Nerve|April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort StudyAlexandre Guérémy, V Morel, T Stojkovic, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Clinical Genetics|January 6, 2011
Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?M Krahn, M Goicoechea, F Hanisch, et al.
Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Neuropathology and Applied Neurobiology|April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathyM Cerino, E Campana-Salort, A Salvi, et al.
Neurology|May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.
Annals of Neurology|August 1, 1997
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in TurkeyP Dinçer, F Leturcq, I Richard, et al.
Diabetes Care|July 8, 1998
Factors associated with glycemic control. A cross-sectional nationwide study in 2,579 French children with type 1 diabetes. The French Pediatric Diabetes GroupM Rosilio, J B Cotton, M C Wieliczko, et al.
European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Brain : a Journal of Neurology|February 4, 2005
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 geneA Sáenz, F Leturcq, A M Cobo, et al.
Muscle & Nerve|April 7, 2026
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort StudyAlexandre Guérémy, V Morel, T Stojkovic, et al.
Pageof 5