Setareh Ashtiani
Calgary, AB, Canada
Last Updated: 09/26/2026
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Found 12 publications
Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disorders.
Journal: BMC medicine
Published: July 29, 2025
Identification of a Second-Hit Brain Somatic DEPDC5 Variant Supports Causality of a DEPDC5 Germline Variant of Uncertain Significance. Time for a Classification Update?
Journal: American journal of medical genetics. Part A
Published: April 16, 2025
Hereditary Spastic Paraplegia in Alberta: Lessons from a Well-Defined Cohort Including the Indigenous Population.
Journal: Movement disorders clinical practice
Published: November 05, 2024
EEFSEC deficiency: A selenopathy with early-onset neurodegeneration.
Journal: American journal of human genetics
Published: June 07, 2024
Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies.
Journal: Brain communications
Published: January 09, 2023
Genetic, structural and clinical analysis of spastic paraplegia 4.
Journal: Parkinsonism & related disorders
Published: January 25, 2022
Hereditary spastic paraplegia initially diagnosed as cerebral palsy.
Journal: Clinical parkinsonism & related disorders
Published: August 20, 2021
CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia.
Journal: European journal of medical genetics
Published: June 22, 2018
Clinical and genetic study of hereditary spastic paraplegia in Canada.
Journal: Neurology. Genetics
Published: June 30, 2016
Parents' experiences of receiving their child's genetic diagnosis: a qualitative study to inform clinical genetics practice.
Journal: American journal of medical genetics. Part A
Published: October 29, 2013
Showing 1-12 of 12
Last Updated: 09/26/2026