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C Angelini

Showing results (181-190 of 531) with videos related to

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Minerva Chirurgica|July 19, 2001
[Serious complications of vertical banded gastroplasty. Case report]C M Franciosi, C Mussi, C Angelini, et al.
Neurology|January 28, 1999
The clinical spectrum of sarcoglycanopathiesC Angelini, M Fanin, M P Freda, et al.
Lancet (London, England)|March 4, 1995
Prenatal diagnosis in congenital muscular dystrophyF Muntoni, C Sewry, L Wilson, et al.
Journal of Medical Genetics|May 29, 2007
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2AM Fanin, L Nardetto, A C Nascimbeni, et al.
Mitochondrion|May 23, 2009
Two novel cosegregating mutations in tRNAMet and COX III, in a patient with exercise intolerance and autoimmune polyendocrinopathyB Bortot, E Barbi, S Biffi, et al.
Chemosphere|December 5, 1998
Biological effects of a neurotoxic pesticide at low concentrations on sea urchin early development. A terathogenic assayA Morale, L Coniglio, C Angelini, et al.
Muscle & Nerve|March 1, 1996
Residual muscle cytochrome c oxidase activity accounts for submaximal exercise lactate threshold in chronic progressive external ophthalmoplegiaG Siciliano, B Rossi, L Manca, et al.
European Journal of Neurology|April 21, 2010
EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemiaT Kyriakides, C Angelini, J Schaefer, et al.
Journal of Endocrinological Investigation|May 1, 1994
Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutationI Mastrogiacomo, E Pagani, G Novelli, et al.
Journal of Medical Genetics|February 1, 1992
Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patientsL Vitiello, M L Mostacciuolo, S Oliviero, et al.
Pageof 54

Showing results (181-190 of 531) with videos related to

Sort By:
Pageof 54
Minerva Chirurgica|July 19, 2001
[Serious complications of vertical banded gastroplasty. Case report]C M Franciosi, C Mussi, C Angelini, et al.
Neurology|January 28, 1999
The clinical spectrum of sarcoglycanopathiesC Angelini, M Fanin, M P Freda, et al.
Lancet (London, England)|March 4, 1995
Prenatal diagnosis in congenital muscular dystrophyF Muntoni, C Sewry, L Wilson, et al.
Journal of Medical Genetics|May 29, 2007
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2AM Fanin, L Nardetto, A C Nascimbeni, et al.
Mitochondrion|May 23, 2009
Two novel cosegregating mutations in tRNAMet and COX III, in a patient with exercise intolerance and autoimmune polyendocrinopathyB Bortot, E Barbi, S Biffi, et al.
Chemosphere|December 5, 1998
Biological effects of a neurotoxic pesticide at low concentrations on sea urchin early development. A terathogenic assayA Morale, L Coniglio, C Angelini, et al.
Muscle & Nerve|March 1, 1996
Residual muscle cytochrome c oxidase activity accounts for submaximal exercise lactate threshold in chronic progressive external ophthalmoplegiaG Siciliano, B Rossi, L Manca, et al.
European Journal of Neurology|April 21, 2010
EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemiaT Kyriakides, C Angelini, J Schaefer, et al.
Journal of Endocrinological Investigation|May 1, 1994
Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutationI Mastrogiacomo, E Pagani, G Novelli, et al.
Journal of Medical Genetics|February 1, 1992
Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patientsL Vitiello, M L Mostacciuolo, S Oliviero, et al.
Pageof 54