Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications.
Shan, Din-E
Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications. [electronic resource] - Movement disorders : official journal of the Movement Disorder Society Nov 2004 - 1357-60 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0885-3185
10.1002/mds.20212 doi
Aged
Alleles
Antiparkinson Agents--therapeutic use
Ataxins
Caudate Nucleus--diagnostic imaging
DNA Mutational Analysis
Dominance, Cerebral--physiology
Genetic Carrier Screening
Genetic Testing
Humans
Levodopa--therapeutic use
Male
Middle Aged
Nerve Tissue Proteins
Neurologic Examination
Parkinson Disease--diagnostic imaging
Polymerase Chain Reaction
Positron-Emission Tomography
Proteins--genetics
Putamen--diagnostic imaging
Spinocerebellar Ataxias--diagnostic imaging
Treatment Outcome
Trinucleotide Repeats
Ubiquitin-Protein Ligases--genetics
Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications. [electronic resource] - Movement disorders : official journal of the Movement Disorder Society Nov 2004 - 1357-60 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0885-3185
10.1002/mds.20212 doi
Aged
Alleles
Antiparkinson Agents--therapeutic use
Ataxins
Caudate Nucleus--diagnostic imaging
DNA Mutational Analysis
Dominance, Cerebral--physiology
Genetic Carrier Screening
Genetic Testing
Humans
Levodopa--therapeutic use
Male
Middle Aged
Nerve Tissue Proteins
Neurologic Examination
Parkinson Disease--diagnostic imaging
Polymerase Chain Reaction
Positron-Emission Tomography
Proteins--genetics
Putamen--diagnostic imaging
Spinocerebellar Ataxias--diagnostic imaging
Treatment Outcome
Trinucleotide Repeats
Ubiquitin-Protein Ligases--genetics