Oksana Suchowersky

Edmonton, AB, Canada

Last Updated: 09/26/2026

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Found 75 publications

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Journal: CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne
Published: January 26, 2026

MDSGene Systematic Review of Common Forms of Dominant Hereditary Spastic Paraplegia: Novel Insights.

MDSGene Systematic Review of Common Forms of Dominant Hereditary Spastic Paraplegia: Novel Insights.

Journal: Movement disorders clinical practice
Published: December 24, 2025

Reprint of : First case of Cayman ataxia far north of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY gene.

Reprint of : First case of Cayman ataxia far north of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY gene.

Journal: Parkinsonism & related disorders
Published: November 06, 2025

Identification of an additional deep intronic splice variant prompts critical evaluation of SPG7 inheritance.

Identification of an additional deep intronic splice variant prompts critical evaluation of SPG7 inheritance.

Journal: Neurogenetics
Published: October 10, 2025

Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.

Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 24, 2025

Best practice recommendations for the clinical care of spinal bulbar muscular atrophy.

Best practice recommendations for the clinical care of spinal bulbar muscular atrophy.

Journal: CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne
Published: September 22, 2025

Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disorders.

Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disorders.

Journal: BMC medicine
Published: July 29, 2025

Never Late: Cerebrotendinous Xanthomatosis and Improvements in Neurocognitive Functions in an Adult Patient on Chenodeoxycholic Acid Treatment.

Never Late: Cerebrotendinous Xanthomatosis and Improvements in Neurocognitive Functions in an Adult Patient on Chenodeoxycholic Acid Treatment.

Journal: Clinical genetics
Published: February 24, 2025

Therapeutic modalities of deferiprone in Parkinson's disease: SKY and EMBARK studies.

Therapeutic modalities of deferiprone in Parkinson's disease: SKY and EMBARK studies.

Journal: Journal of Parkinson's disease
Published: February 20, 2025

First case of Cayman ataxia far north of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY gene.

First case of Cayman ataxia far north of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY gene.

Journal: Parkinsonism & related disorders
Published: February 17, 2025

Rare Spinocerebellar Ataxia Types in Canada: A Case Series and Review of the Literature.

Rare Spinocerebellar Ataxia Types in Canada: A Case Series and Review of the Literature.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: December 02, 2024

Hereditary Spastic Paraplegia in Alberta: Lessons from a Well-Defined Cohort Including the Indigenous Population.

Hereditary Spastic Paraplegia in Alberta: Lessons from a Well-Defined Cohort Including the Indigenous Population.

Journal: Movement disorders clinical practice
Published: November 05, 2024
Showing 1-12 of 75

Last Updated: 09/26/2026