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American Journal of Medical Genetics. Part A|April 8, 2014
Parents' experiences of receiving their child's genetic diagnosis: a qualitative study to inform clinical genetics practiceSetareh Ashtiani, Nancy Makela, Prescilla Carrion, et al.
Clinical Parkinsonism & Related Disorders|November 24, 2021
Hereditary spastic paraplegia initially diagnosed as cerebral palsyOksana Suchowersky, Setareh Ashtiani, Ping-Yee Billie Au, et al.
Movement Disorders Clinical Practice|May 5, 2025
Hereditary Spastic Paraplegia in Alberta: Lessons from a Well-Defined Cohort Including the Indigenous PopulationEkhlas Assaedi, Setareh Ashtiani, Mehrdad A Estiar, et al.
Journal of Neurology|September 19, 2021
The phenotypic spectrum of KCNT1: a new family with variable epilepsy syndromes including mild focal epilepsyChristina Cherian, Juan P Appendino, Setareh Ashtiani, et al.
European Journal of Medical Genetics|December 21, 2018
CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxiaAakash Shetty, Ziv Gan-Or, Setareh Ashtiani, et al.
Neurogenetics|February 8, 2026
Identification of an additional deep intronic splice variant prompts critical evaluation of SPG7 inheritanceEmma H Gillesse, Miranda Wan, Setareh Ashtiani, et al.
Parkinsonism & Related Disorders|April 29, 2022
Genetic, structural and clinical analysis of spastic paraplegia 4Parizad Varghaei, Mehrdad A Estiar, Setareh Ashtiani, et al.
Neurology. Genetics|December 14, 2016
Clinical and genetic study of hereditary spastic paraplegia in CanadaNicolas Chrestian, Nicolas Dupré, Ziv Gan-Or, et al.
BMC Medicine|March 25, 2026
Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disordersMehrdad A Estiar, Eric Yu, Parizad Varghaei, et al.
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