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1. The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.

Authors: H Y Zoghbi; C Jodice; L A Sandkuijl; T J Kwiatkowski; A E McCall; S A Huntoon; P Lulli; M Spadaro; M Litt; H M Cann
Journal: Am J Hum Genet Date: 1991-07 Impact factor: 11.025

Review 2. Progress in pathogenesis studies of spinocerebellar ataxia type 1.

Authors: C J Cummings; H T Orr; H Y Zoghbi
Journal: Philos Trans R Soc Lond B Biol Sci Date: 1999-06-29 Impact factor: 6.237

3. Cytoplasmic argyrophilic inclusions in neurons of pontine nuclei in patients with olivopontocerebellar atrophy: immunohistochemical and ultrastructural studies.

Authors: S Kato; H Nakamura
Journal: Acta Neuropathol Date: 1990 Impact factor: 17.088

4. Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis.

Authors: H Y Zoghbi; L A Sandkuyl; J Ott; S P Daiger; M Pollack; W E O'Brien; A L Beaudet
Journal: Am J Hum Genet Date: 1989-02 Impact factor: 11.025

5. Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disorders.

Authors: D Aubby; H K Saggu; P Jenner; N P Quinn; A E Harding; C D Marsden
Journal: J Neurol Neurosurg Psychiatry Date: 1988-07 Impact factor: 10.154

5 in total