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I Richard

Showing results (111-120 of 157) with videos related to

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Journal of Medical Genetics|May 1, 1993
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian familiesM R Passos-Bueno, I Richard, M Vainzof, et al.
The American Journal of Pathology|October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2AL V Anderson, K Davison, J A Moss, et al.
Microorganisms|January 23, 2020
Inter- Versus Intra-Host Sequence Diversity of pH1N1 and Associated Clinical OutcomesHebah A Al Khatib, Muna A Al Maslamani, Peter V Coyle, et al.
Brain : a Journal of Neurology|March 6, 2007
Zaspopathy in a large classic late-onset distal myopathy familyR Griggs, A Vihola, P Hackman, et al.
Physical Review Letters|March 5, 2009
Enhanced relaxation and intermixing in Ge islands grown on pit-patterned Si(001) substratesT U Schülli, G Vastola, M-I Richard, et al.
Brain : a Journal of Neurology|February 1, 1996
Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion IslandM Fardeau, D Hillaire, C Mignard, et al.
Clinical Neurology and Neurosurgery|March 18, 2008
An autopsy case of acute multiple sclerosis (Marburg's type) during pregnancyF Letournel, J Cassereau, C Scherer-Gagou, et al.
Molecular and Cellular Biology|May 18, 1999
Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional eventsM Herasse, Y Ono, F Fougerousse, et al.
Neurology|April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
Pageof 16

Showing results (111-120 of 157) with videos related to

Sort By:
Pageof 16
Journal of Medical Genetics|May 1, 1993
Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian familiesM R Passos-Bueno, I Richard, M Vainzof, et al.
The American Journal of Pathology|October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2AL V Anderson, K Davison, J A Moss, et al.
Microorganisms|January 23, 2020
Inter- Versus Intra-Host Sequence Diversity of pH1N1 and Associated Clinical OutcomesHebah A Al Khatib, Muna A Al Maslamani, Peter V Coyle, et al.
Brain : a Journal of Neurology|March 6, 2007
Zaspopathy in a large classic late-onset distal myopathy familyR Griggs, A Vihola, P Hackman, et al.
Physical Review Letters|March 5, 2009
Enhanced relaxation and intermixing in Ge islands grown on pit-patterned Si(001) substratesT U Schülli, G Vastola, M-I Richard, et al.
Brain : a Journal of Neurology|February 1, 1996
Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion IslandM Fardeau, D Hillaire, C Mignard, et al.
Clinical Neurology and Neurosurgery|March 18, 2008
An autopsy case of acute multiple sclerosis (Marburg's type) during pregnancyF Letournel, J Cassereau, C Scherer-Gagou, et al.
Molecular and Cellular Biology|May 18, 1999
Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional eventsM Herasse, Y Ono, F Fougerousse, et al.
Neurology|April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
Pageof 16