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Movement Disorders (revue) - Curation (Ncbi)

Index « Keywords » - entrée « Machado-Joseph Disease (diagnosis) »
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List of bibliographic references

Number of relevant bibliographic references: 7.
Ident.Authors (with country if any)Title
000953 (2002) Joseph H. Friedman [États-Unis]Presumed rapid eye movement behavior disorder in Machado-Joseph disease (spinocerebellar ataxia type 3).
000C99 (2004) Jacob Appel ; Joseph H. FriedmanGenetic markers and the majority's right not to know.
001622 (2006) José Berciano [Espagne] ; Jon Infante ; Antonio García ; Carmen De Pablos ; Guillermo Amer ; José Miguel Polo ; Victor Volpini ; Onofre CombarrosStiff man-like syndrome and generalized myokymia in spinocerebellar ataxia type 3.
001649 (2006) Marcondes C. França [Brésil] ; Maria E. Calcagnotto ; Jaderson C. Da Costa ; Iscia Lopes-CendesSpinocerebellar ataxia types 2 and 3 segregating simultaneously in a single family.
001E35 (2007) Anelyssa D'Abreu [Brésil] ; Marcondes Franca ; Iscia Lopes-Cendes ; Fernando CendesThe international cooperative ataxia rating scale in Machado-Joseph disease. Comparison with the unified multiple system atrophy rating scale.
004A78 (1996) S H Subramony [États-Unis] ; J D Fratkin ; B V Manyam ; R D CurrierDominantly 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.
004C34 (1996) S H Subramony [États-Unis] ; R D CurrierIntrafamilial variability in Machado-Joseph disease.

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