Michel Sylvain
Quebec, QC, Canada
Last Updated: 09/26/2026
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Found 8 publications
Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophy.
Journal: Molecular genetics and metabolism
Published: March 19, 2024
Craniofacial features of POLR3-related leukodystrophy caused by biallelic variants in POLR3A, POLR3B and POLR1C.
Journal: Journal of medical genetics
Published: February 16, 2023
Solving inherited white matter disorder etiologies in the neurology clinic: Challenges and lessons learned using next-generation sequencing.
Journal: Frontiers in neurology
Published: January 20, 2023
Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot Study.
Journal: Journal of child neurology
Published: July 29, 2020
Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C.
Journal: The Journal of clinical endocrinology and metabolism
Published: May 29, 2020
Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness.
Journal: American journal of human genetics
Published: February 20, 2014
Tremor-ataxia with central hypomyelination (TACH): dystonia as a new clinical feature.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 06, 2012
TACH leukodystrophy: locus refinement to chromosome 10q22.3-23.1.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: March 06, 2012
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Last Updated: 09/26/2026