Nassima Boudrahem-Addour
Montreal, QC, Canada
Last Updated: 09/26/2026
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Found 8 publications
Posterior Fossa Malformations in a Cohort of 116 Fetuses: A Retrospective Analysis of Imaging Characteristics, Postnatal Imaging Concordance, Pregnancy Outcomes and Yield of Genetic Testing.
Journal: Cerebellum (London, England)
Published: June 30, 2025
mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development: Novel Variants, Topographic Mapping, and Clinical Outcomes.
Journal: Neurology. Genetics
Published: April 21, 2023
Classic "PCH" Genes are a Rare Cause of Radiologic Pontocerebellar Hypoplasia.
Journal: Cerebellum (London, England)
Published: March 08, 2023
PCDH12 variants are associated with basal ganglia anomalies and exudative vitreoretinopathy.
Journal: European journal of medical genetics
Published: May 25, 2021
Diagnostic Approach to Cerebellar Hypoplasia.
Journal: Cerebellum (London, England)
Published: December 02, 2020
Neurogenesis, neuronal migration, and axon guidance.
Journal: Handbook of clinical neurology
Published: September 22, 2020
Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia.
Journal: Journal of child neurology
Published: October 17, 2019
Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia.
Journal: Neurogenetics
Published: December 23, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026