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F Piccolo

Showing results (21-30 of 32) with videos related to

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European Journal of Human Genetics : EJHG|October 22, 1998
Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan geneA Lasa, F Piccolo, C de Diego, et al.
Alimentary Pharmacology & Therapeutics|January 6, 2006
Switch therapy with ciprofloxacin vs. intravenous ceftazidime in the treatment of spontaneous bacterial peritonitis in patients with cirrhosis: similar efficacy at lower costP Angeli, S Guarda, S Fasolato, et al.
Human Molecular Genetics|December 1, 1994
Adhalin gene polymorphismV Allamand, F Leturcq, F Piccolo, et al.
Cell|August 26, 1994
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophyS L Roberds, F Leturcq, V Allamand, et al.
European Journal of Neurology|May 15, 2014
Large deletion mutation of SPAST in a multi-generation family from SardiniaL Racis, R Di Fabio, A Tessa, et al.
Neuromuscular Disorders : NMD|December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overviewM Jeanpierre, A Carrié, F Piccolo, et al.
Human Molecular Genetics|December 1, 1996
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of IndiaF Piccolo, M Jeanpierre, F Leturcq, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, 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.
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.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
European Journal of Human Genetics : EJHG|October 22, 1998
Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan geneA Lasa, F Piccolo, C de Diego, et al.
Alimentary Pharmacology & Therapeutics|January 6, 2006
Switch therapy with ciprofloxacin vs. intravenous ceftazidime in the treatment of spontaneous bacterial peritonitis in patients with cirrhosis: similar efficacy at lower costP Angeli, S Guarda, S Fasolato, et al.
Human Molecular Genetics|December 1, 1994
Adhalin gene polymorphismV Allamand, F Leturcq, F Piccolo, et al.
Cell|August 26, 1994
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophyS L Roberds, F Leturcq, V Allamand, et al.
European Journal of Neurology|May 15, 2014
Large deletion mutation of SPAST in a multi-generation family from SardiniaL Racis, R Di Fabio, A Tessa, et al.
Neuromuscular Disorders : NMD|December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overviewM Jeanpierre, A Carrié, F Piccolo, et al.
Human Molecular Genetics|December 1, 1996
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of IndiaF Piccolo, M Jeanpierre, F Leturcq, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, 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.
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.
Pageof 4