État du Mississippi And NotLisa S. Friedman
List of bibliographic references
Number of relevant bibliographic references: 9.| Ident. | Authors (with country if any) | Title |
|---|---|---|
| 002678 | Alison La Pean [États-Unis] ; Neal Jeffries [États-Unis] ; Chelsea Grow [États-Unis] ; Bernard Ravina [États-Unis] ; Nicholas A. Di Prospero [États-Unis] | Predictors of progression in patients with Friedreich ataxia |
| 003974 | Matthias Maschke [Allemagne] ; Gary Oehlert [États-Unis] ; Ting-Dong Xie [États-Unis] ; Susan Perlman [États-Unis] ; Sub H. Subramony [États-Unis] ; Neeraj Kumar [États-Unis] ; Louis J. Ptacek [États-Unis] ; Christopher M. Gomez [États-Unis] | Clinical feature profile of spinocerebellar ataxia type 1–8 predicts genetically defined subtypes |
| 003F06 | Roy R. Reeves [États-Unis] ; Vincent Liberto [États-Unis] | Treatment of essential blepharospasm with quetiapine |
| 004469 | S. H. Subramony [États-Unis] ; Dena Hernandez [États-Unis] ; Amanda Adam [États-Unis] ; Stephanie Smith-Jefferson [États-Unis] ; Jennifer Hussey [États-Unis] ; Katrina Gwinn-Hardy [États-Unis] ; Timothy Lynch [États-Unis, Irlande (pays)] ; Olga Mcdaniel [États-Unis] ; John Hardy [États-Unis, Royaume-Uni] ; Matt Farrer [États-Unis] ; Andrew Singleton [États-Unis] | Ethnic differences in the expression of neurodegenerative disease: Machado‐Joseph disease in Africans and Caucasians |
| 004688 | D. Olga Mcdaniel [États-Unis] ; Bronya Keats [États-Unis] ; V. V. Vedanarayanan [États-Unis] ; S. H. Subramony [États-Unis] | Sequence variation in GAA repeat expansions may cause differential penotype display in Friedreich's ataxia |
| 005666 | Subramony [États-Unis] ; J. D. Fratkin [États-Unis] ; B. V. Manyam [États-Unis] ; R. D. Currier [États-Unis] | Dominantly inherited cerebello‐olivary atrophy is not due to a mutation at the spinocerebellar ataxia‐I, machado‐joseph disease, or dentato‐rubro‐pallido‐luysian atrophy locus |
| 005761 | S. H. Subramony [États-Unis] ; R. D. Currier [États-Unis] | Intrafamilial variability in Machado-Joseph disease |
| 005772 | S. H. Subramony [États-Unis] ; J. D. Fratkin ; B. V. Manyam ; R. D. Currier [États-Unis] | Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or dentato-rubro-pallido-luysian atrophy locus |
| 005824 | Xiao-Hui Zhong [Canada] ; John W. Haycock [États-Unis] ; Kathleen Shannak [Canada] ; Yves Robitaille [Canada] ; Jonathan Fratkin [États-Unis] ; Arnuf H. Koeppen [États-Unis] ; Oleh Hornykiewicz [Canada, Autriche] ; Kish [Canada] | Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophy |
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