Detalhe da pesquisa
1.
Clinical Trial-Ready Patient Cohorts for Multiple System Atrophy: Coupling Biospecimen and iPSC Banking to Longitudinal Deep-Phenotyping.
Cerebellum
; 2022 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36190676
2.
Functional validation of novel variants in B4GALNT1 associated with early-onset complex hereditary spastic paraplegia with impaired ganglioside synthesis.
Am J Med Genet A
; 188(9): 2590-2598, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35775650
3.
Correction to: Clinical trial-ready patient cohorts for multiple system atrophy: coupling biospecimen and iPSC banking to longitudinal deep-phenotyping.
Cerebellum
; 2022 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36456723
4.
Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology.
Mov Disord Clin Pract
; 11(4): 411-423, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38258626
5.
Transition From Pediatric to Adult Neurologic Care.
Continuum (Minneap Minn)
; 24(1, Child Neurology): 276-287, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29432247