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M Vanasse

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The New England Journal of Medicine|February 15, 1990
Neurologic crises in hereditary tyrosinemiaG Mitchell, J Larochelle, M Lambert, et al.
Annals of Neurology|July 1, 1993
Myoblast transfer in Duchenne muscular dystrophyG Karpati, D Ajdukovic, D Arnold, et al.
Neurogenetics|March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.
The Journal of Pediatrics|November 1, 1992
Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patientsJ F Lemay, M A Lambert, G A Mitchell, et al.
Brain : a Journal of Neurology|June 9, 2006
A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21M Tétreault, A Duquette, I Thiffault, et al.
American Journal of Medical Genetics. Part A|October 26, 2022
Teaching perspectives on the communication of difficult news of genetic conditions to medical studentsAshley M Vanasse, Tracey Weiler, Elizabeth A Roth, et al.
Lancet (London, England)|September 18, 2001
Hyperbaric oxygen for children with cerebral palsy: a randomised multicentre trial. HBO-CP Research GroupJ P Collet, M Vanasse, P Marois, et al.
Brain : a Journal of Neurology|May 5, 2006
A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34I Thiffault, M F Rioux, M Tetreault, et al.
Neurology|May 25, 2005
Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French CanadiansK Roddier, T Thomas, G Marleau, et al.
Annals of Neurology|May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansionL Montermini, A Richter, K Morgan, 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.
The New England Journal of Medicine|February 15, 1990
Neurologic crises in hereditary tyrosinemiaG Mitchell, J Larochelle, M Lambert, et al.
Annals of Neurology|July 1, 1993
Myoblast transfer in Duchenne muscular dystrophyG Karpati, D Ajdukovic, D Arnold, et al.
Neurogenetics|March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.
The Journal of Pediatrics|November 1, 1992
Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patientsJ F Lemay, M A Lambert, G A Mitchell, et al.
Brain : a Journal of Neurology|June 9, 2006
A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21M Tétreault, A Duquette, I Thiffault, et al.
American Journal of Medical Genetics. Part A|October 26, 2022
Teaching perspectives on the communication of difficult news of genetic conditions to medical studentsAshley M Vanasse, Tracey Weiler, Elizabeth A Roth, et al.
Lancet (London, England)|September 18, 2001
Hyperbaric oxygen for children with cerebral palsy: a randomised multicentre trial. HBO-CP Research GroupJ P Collet, M Vanasse, P Marois, et al.
Brain : a Journal of Neurology|May 5, 2006
A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34I Thiffault, M F Rioux, M Tetreault, et al.
Neurology|May 25, 2005
Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French CanadiansK Roddier, T Thomas, G Marleau, et al.
Annals of Neurology|May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansionL Montermini, A Richter, K Morgan, et al.
Pageof 5