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Nicolas Chrestian

Showing results (21-30 of 24) with videos related to

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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 13, 2024
Equitable Access to Disease-Modifying Therapies for Canadian Children with SMA and Four <i>SMN2</i> CopiesHugh J McMillan, Hernan Gonorazky, Craig Campbell, 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.
American Journal of Human Genetics|September 29, 2021
ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomaliesGabrielle Lemire, Yoko A Ito, Aren E Marshall, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 5, 2020
A National Spinal Muscular Atrophy Registry for Real-World EvidenceVictoria L Hodgkinson, Maryam Oskoui, Joshua Lounsberry, et al.
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Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 13, 2024
Equitable Access to Disease-Modifying Therapies for Canadian Children with SMA and Four <i>SMN2</i> CopiesHugh J McMillan, Hernan Gonorazky, Craig Campbell, 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.
American Journal of Human Genetics|September 29, 2021
ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomaliesGabrielle Lemire, Yoko A Ito, Aren E Marshall, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 5, 2020
A National Spinal Muscular Atrophy Registry for Real-World EvidenceVictoria L Hodgkinson, Maryam Oskoui, Joshua Lounsberry, et al.
Pageof 3