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SCA8 should not be tested in isolation for ataxia

Roda, Ricardo H.; Schindler, Alice B.; Blackstone, Craig

Neurology. Volume 3:Number 3(2017); 201706; - -- [Wolters Kluwer]

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SCA8 should not be tested in isolation for ataxia

Roda, Ricardo H.; Schindler, Alice B.; Blackstone, Craig

Neurology. Genetics. Volume 3:Number 3 (2017) -- [Wolters Kluwer]

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De novo REEP2 missense mutation in pure hereditary spastic paraplegia

Roda, Ricardo H.; Schindler, Alice B.; Blackstone, Craig

Annals of clinical and translational neurology. Volume 4:Issue 5 (2017); pp 347-350 -- Wiley Periodicals, Inc on behalf of American Neurological Association

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Multigeneration family with dominant SPG30 hereditary spastic paraplegia

Roda, Ricardo H.; Schindler, Alice B.; Blackstone, Craig

Annals of clinical and translational neurology. Volume 4:Issue 11 (2017); pp 821-824 -- Wiley Periodicals, Inc on behalf of American Neurological Association

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Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site

Roda, Ricardo H. et al.

Annals of clinical and translational neurology. Volume 3:Issue 8 (2016); pp 650-654 -- Wiley Periodicals, Inc on behalf of American Neurological Association

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TUBB2B Mutation in an Adult Patient with Myoclonus-Dystonia

Geiger, Joshua T. et al.

Case reports in neurology. Volume 9:Number 2 (2017, August 31st); pp 216-221 -- Karger

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Nucleocytoplasmic transport defect in a North American patient with ALS8

Guber, Robert D. et al.

Annals of clinical and translational neurology. Volume 5:Issue 3 (2018); pp 369-375 -- Wiley Periodicals, Inc on behalf of American Neurological Association

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Patient‐identified impact of symptoms in spinal and bulbar muscular atrophy

Guber, Robert D. et al.

Muscle & nerve. Volume 57:Issue 1 (2018); pp 40-44 -- John Wiley & Sons

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Laing distal myopathy pathologically resembling inclusion body myositis

Roda, Ricardo H. et al.

Annals of clinical and translational neurology. Volume 1:Number 12 (2014); pp 1053-1058 -- Wiley Periodicals, Inc on behalf of American Neurological Association

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A Review of Genetic Counseling for Charcot Marie Tooth Disease (CMT)

Siskind, Carly E. et al.

Journal of genetic counseling. Volume 22:Issue 4 (2013); pp 422-436 -- Wiley Periodicals, Inc

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