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M Vanasse

Showing results (31-40 of 50) with videos related to

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Genomics|September 1, 1992
Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian familiesL R Simard, M Vanasse, C Rochette, et al.
Undersea & Hyperbaric Medicine : Journal of the Undersea and Hyperbaric Medical Society, Inc|January 21, 2000
Effects of hyperbaric oxygen therapy on children with spastic diplegic cerebral palsy: a pilot projectD Montgomery, J Goldberg, M Amar, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1982
Oral lecithin and linoleic acid in Friedreich's ataxia: II. Clinical resultsS B Melancon, M Vanasse, G Geoffroy, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 1, 1995
Alu-PCR combined with non-Alu primers reveals multiple polymorphic lociJ Q Tang, M Korab-Laskowska, M Jarnik, et al.
Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1990
Utility of short-latency evoked potentials in the classification of progressive, early onset cerebellar ataxiasM Vanasse, J Y Gabet, J De Léan, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1982
Oral lecithin and linoleic acid in Friedreich's ataxia: III. Biochemical resultsS B Melancon, L Dallaire, M Potier, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 19, 1999
Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplicationN Dupré, J P Bouchard, L Cossette, et al.
Human Molecular Genetics|March 1, 1994
Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian populationL R Simard, G Prescott, C Rochette, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
<i>LPIN1</i> deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomyI A Meijer, F Sasarman, C Maftei, et al.
Pediatric Research|June 1, 1986
Auditory brainstem response audiometry in congenitally hypothyroid children under early replacement therapyR Hébert, E Laureau, M Vanasse, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Genomics|September 1, 1992
Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian familiesL R Simard, M Vanasse, C Rochette, et al.
Undersea & Hyperbaric Medicine : Journal of the Undersea and Hyperbaric Medical Society, Inc|January 21, 2000
Effects of hyperbaric oxygen therapy on children with spastic diplegic cerebral palsy: a pilot projectD Montgomery, J Goldberg, M Amar, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1982
Oral lecithin and linoleic acid in Friedreich's ataxia: II. Clinical resultsS B Melancon, M Vanasse, G Geoffroy, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 1, 1995
Alu-PCR combined with non-Alu primers reveals multiple polymorphic lociJ Q Tang, M Korab-Laskowska, M Jarnik, et al.
Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1990
Utility of short-latency evoked potentials in the classification of progressive, early onset cerebellar ataxiasM Vanasse, J Y Gabet, J De Léan, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1982
Oral lecithin and linoleic acid in Friedreich's ataxia: III. Biochemical resultsS B Melancon, L Dallaire, M Potier, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 19, 1999
Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplicationN Dupré, J P Bouchard, L Cossette, et al.
Human Molecular Genetics|March 1, 1994
Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian populationL R Simard, G Prescott, C Rochette, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
<i>LPIN1</i> deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomyI A Meijer, F Sasarman, C Maftei, et al.
Pediatric Research|June 1, 1986
Auditory brainstem response audiometry in congenitally hypothyroid children under early replacement therapyR Hébert, E Laureau, M Vanasse, et al.
Pageof 5