K Gwinn Hardy
Affiliation: Mayo Clinic
- Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4pK Gwinn-Hardy
Department of Neurology, Mayo Clinic Jacksonville, FL 32224, USA
Acta Neuropathol 99:663-72. 2000..We also discuss the relationship of this familial disorder to a Lewy body disease clinical spectrum, ranging from Parkinson's disease to dementia with psychosis...
- Spinocerebellar ataxia type 2 with parkinsonism in ethnic ChineseK Gwinn-Hardy
Departments of Neurology and Pharmacology, Mayo Clinic Jacksonville, FL 32224, USA
Neurology 55:800-5. 2000..To describe the clinical and molecular genetic analysis of a large family of northern Chinese descent with a mutation at the SCA2 locus causing carbidopa-levodopa-responsive parkinsonism...
- Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black familyK Gwinn-Hardy
Mayo Clinic Jacksonville, 4500 San Pablo Rd, Jacksonville, FL 32224, USA
Arch Neurol 58:296-9. 2001..However, classically, atypical features, including pyramidal and cerebellar signs, peripheral neuropathy, and/or anterior horn cell dysfunction, are also seen. Levodopa responsiveness is unusual in this disorder...
- Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesiaM K Bruno
Department of Neurology, University of California, San Francisco, CA 94158, USA
Neurology 68:1782-9. 2007..Paroxysmal nonkinesigenic dyskinesia (PNKD) is a rare disorder characterized by episodic hyperkinetic movement attacks. We have recently identified mutations in the MR-1 gene causing familial PNKD...