K Gwinn Hardy

Summary

Affiliation: Mayo Clinic
Country: USA

Publications

  1. ncbi Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p
    K Gwinn-Hardy
    Department of Neurology, Mayo Clinic Jacksonville, FL 32224, USA
    Acta Neuropathol 99:663-72. 2000
  2. ncbi Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese
    K Gwinn-Hardy
    Departments of Neurology and Pharmacology, Mayo Clinic Jacksonville, FL 32224, USA
    Neurology 55:800-5. 2000
  3. ncbi Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family
    K Gwinn-Hardy
    Mayo Clinic Jacksonville, 4500 San Pablo Rd, Jacksonville, FL 32224, USA
    Arch Neurol 58:296-9. 2001
  4. ncbi Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia
    M K Bruno
    Department of Neurology, University of California, San Francisco, CA 94158, USA
    Neurology 68:1782-9. 2007

Collaborators

  • J Hardy
  • A Friedman
  • P Van Bogaert
  • M Hallett
  • J Y Chen
  • M Pandolfo
  • J E Nielsen
  • K Gwinn-Hardy
  • M K Bruno
  • M Farrer
  • A Singleton
  • M Boss
  • A Adam
  • E Bertini
  • H-Y Lee
  • H Y Lee
  • L Ptacek
  • B Sorenson
  • H Kwiecinski
  • Y-H Fu
  • G W J Auburger
  • Y Averyanov
  • S Servidei
  • Y H Fu
  • A E Lang
  • P Critchley
  • J Hussey
  • P O'Suilleabhain
  • D Nicholl
  • S H Yen
  • D Maraganore
  • D W Dickson
  • M Muenter
  • N D Mehta
  • H C Liu
  • C Waters
  • W Seltzer
  • T Y Liu
  • W Koroshetz

Detail Information

Publications4

  1. ncbi Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p
    K 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...
  2. ncbi Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese
    K 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...
  3. ncbi Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family
    K 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...
  4. ncbi Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia
    M 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...