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List of works by Michel Vanasse

A case of secondary dystonia responding to levodopa.

scientific article published on 6 October 2009

A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.

scientific article published on 3 May 2006

A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21.

scientific article published on 7 June 2006

A newborn with spinal muscular atrophy type 0 presenting with a clinicopathological picture suggestive of myotubular myopathy.

scientific article published in November 2007

A progressive neurological syndrome associated with an isolated vitamin E deficiency

scientific article published on 01 November 1984

Acute combined central and peripheral nervous system demyelination in children

scientific article

All-Cause Mortality and Cardiovascular Outcomes With Prophylactic Steroid Therapy in Duchenne Muscular Dystrophy ⬇️

scientific article published on January 23, 2013

Alu-PCR combined with non-Alu primers reveals multiple polymorphic loci

scientific article

An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorder

scientific article

Auditory brainstem response audiometry in congenitally hypothyroid children under early replacement therapy

scientific article published in June 1986

Autosomal dominant juvenile myoclonic epilepsy and GABRA1.

scientific article published in January 2005

Brain tumors in children in a French Canadian environment

scientific article published on August 1, 1979

Carrier status diagnosis in Duchenne muscular dystrophy with "conformational" DNA polymorphism

scientific article published on 01 January 1992

Chronic inflammatory demyelinating polyneuropathy

scientific article published on 01 January 2013

Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplication

scientific article

Clinical and genetic study of chronic (types II and III) childhood onset spinal muscular atrophy

scientific article published on 01 December 1996

Congenital axonal neuropathy and encephalopathy

scientific article published on April 2008

Correlation between serum lipoamide dehydrogenase activity and phosphatidylcholine therapy in Friedreich's ataxia.

scientific article

Critical illness polyneuromyopathy in a child with severe demyelinating myelitis

scientific article published on 4 March 2009

Deflazacort use in Duchenne muscular dystrophy: an 8-year follow-up

scientific article

Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec ⬇️

scientific article published on June 1, 1992

Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophy

scientific article published on 26 August 2016

Efficacy and safety of lacosamide as an adjunctive therapy for refractory focal epilepsy in paediatric patients: a retrospective single-centre study

scientific article

Electromyography in the differential diagnosis of infant hypotonia

scientific article published on 01 April 1982

Evolution and treatment of childhood chronic inflammatory polyneuropathy

scientific article published on 01 February 2007

Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability

scientific article

Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability

scientific journal article

Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster

scientific article

Friedreich's ataxia: malic enzyme activity in cellular fractions of cultured skin fibroblasts

scientific article published on 01 November 1984

Gross Motor Function Measure Evolution Ratio: Use as a Control for Natural Progression in Cerebral Palsy

scientific article published on 17 August 2015

HBO2 and cerebral palsy in children

scholarly article by Pierre Marois & Michel Vanasse published 1 January 2007 in Undersea and Hyperbaric Medicine

Health-Related Quality of Life for Patients With Genetically Determined Leukoencephalopathy

scientific article published on 09 April 2018

Hereditary motor and sensory neuropathy with agenesis of the corpus callosum

scientific article

Hyperbaric oxygen for children with cerebral palsy: a randomised multicentre trial. HBO-CP Research Group

scientific article

Hyperbaric oxygen therapy and cerebral palsy

scientific article published on 01 September 2003

Impaired muscle differentiation in explant cultures of Duchenne muscular dystrophy

scientific article published on 01 February 1984

Intellectual disability without epilepsy associated with STXBP1 disruption

scientific article

Intermittent peripheral weakness as the presenting feature of pyruvate dehydrogenase deficiency

scientific article published on 22 March 2006

Intermittent treatment of febrile convulsions with nitrazepam.

scientific article

Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian population

scientific article published on 01 March 1994

Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian families

scientific article published on 01 September 1992

Lipid profile, fatty acid composition and pro- and anti-oxidant status in pediatric patients with attention-deficit/hyperactivity disorder

scientific article published in July 2008

Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation

scientific article (publication date: September 2007)

Medical and psychosocial considerations in rehabilitation care of childhood neuromuscular diseases

scientific article published on January 1, 2013

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

scientific article (publication date: June 2002)

Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans

scientific article

Myelination Delay and Allan-Herndon-Dudley Syndrome Caused by a Novel Mutation in the SLC16A2 Gene

scientific article published on 7 November 2014

Neurologic crises in hereditary tyrosinemia

scientific article published on 01 February 1990

Neuropsychological effects of hyperbaric oxygen therapy in cerebral palsy

scientific article published in July 2002

Omega-3 fatty acid treatment of children with attention-deficit hyperactivity disorder: A randomized, double-blind, placebo-controlled study

scientific article published on February 2009

Oral lecithin and linoleic acid in Friedreich's ataxia: I. Design of the study, material and methods

scientific article published on 01 May 1982

Oral lecithin and linoleic acid in Friedreich's ataxia: II. Clinical results

scientific article published on May 1982

Oral lecithin and linoleic acid in Friedreich's ataxia: III. Biochemical results

scientific article published on 01 May 1982

Phenotypic Manifestations in French-Canadian Population with Charcot-Marie-Tooth Disease Type 1A Associated with 17p11.2 Duplication

Phenotypic manifestations in French-Canadian populations with Charcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication

scientific article published on 01 September 1999

Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion

scientific article published on 01 May 1997

SMN(T) and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): genotype/phenotype correlations with disease severity

scientific article published on 01 October 1997

Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus

scientific article published on 01 June 1992

Somatosensory evoked potentials and auditory brain-stem responses in congenital hypothyroidism. I. A longitudinal study before and after treatment in six infants detected in the neonatal period

scientific article published in December 1986

Somatosensory evoked potentials and auditory brain-stem responses in congenital hypothyroidism. II. A cross-sectional study in childhood. Correlations with hormonal levels and developmental quotients

scientific article

The Andermann Syndrome: Agenesis of the Corpus Callosum Associated with Mental Retardation and Progressive Sensorimotor Neuronopathy ⬇️

scientific article published on May 1, 1984

The beta-amino acid transport system in Friedreich's ataxia

scientific article published on 01 November 1980

Toxic reactions with valproic acid therapy

scientific article published on 01 May 1981

Transient Creatine Phosphokinase Elevations in Children: A Single-Center Experience ⬇️

scientific article published on May 17, 2011

Tremor-ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3-10q23.31.

scientific article

Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians

scientific article published on 01 May 2005

Utility of short-latency evoked potentials in the classification of progressive, early onset cerebellar ataxias

scientific article published on January 1990

[Congenital myopathies. 9 case reports and general review]

scientific article published on 01 February 1980

[Fucosidosis: 1st Canadian case]

scientific article published on 01 October 1978

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