Detalhe da pesquisa
1.
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families.
Neurodegener Dis
; 17(4-5): 208-212, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28558379
2.
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy.
J Neurol Neurosurg Psychiatry
; 85(5): 486-92, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24198383
3.
Parkinson's Disease Case Ascertainment in the Sister Study: A Cohort for Environmental Health Research.
J Parkinsons Dis
; 13(5): 729-742, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37334620
4.
Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis.
Neurobiol Dis
; 21(1): 102-9, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16084104