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3. [Oligodendroglial inclusions, a marker of multisystemic atrophies]. Costa C; Duyckaerts C; Cervera P; Hauw JJ Rev Neurol (Paris); 1992; 148(4):274-80. PubMed ID: 1332174 [TBL] [Abstract][Full Text] [Related]
4. Differences between multiple system atrophy and olivopontocerebellar atrophy. Quinn N; Daniel S Ann Neurol; 1996 Dec; 40(6):945-6. PubMed ID: 9007105 [No Abstract] [Full Text] [Related]
5. Multiple system atrophy with retinal degeneration in a young child. Nishimura M; Mito T; Takashima S; Kawahara H; Tanaka J; Nakamura H; Kisa T Neuropediatrics; 1987 May; 18(2):91-5. PubMed ID: 3474543 [TBL] [Abstract][Full Text] [Related]
6. An adult case of adrenoleukodystrophy with features of olivo-ponto-cerebellar atrophy: I. Clinical and pathological studies. Takada K; Onoda K; Takahashi K; Nakamura H; Taketomi T Jpn J Exp Med; 1987 Feb; 57(1):53-8. PubMed ID: 3476776 [TBL] [Abstract][Full Text] [Related]
8. [Clinico-pathological study of the central autonomic nervous system in idiopathic parkinsonism--in comparison with sporadic olivopontocerebellar atrophy]. Mitake S; Mizutani T Rinsho Shinkeigaku; 1987 Apr; 27(4):472-8. PubMed ID: 3476231 [No Abstract] [Full Text] [Related]
9. Expression of the endocytosis regulatory proteins Rab5 and Rabaptin-5 in glial cytoplasmic inclusions from brains with multiple system atrophy. Nakamura S; Kawamoto Y; Nakano S; Akiguchi I Clin Neuropathol; 2000; 19(2):51-6. PubMed ID: 10749284 [TBL] [Abstract][Full Text] [Related]
10. Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome). Papp MI; Kahn JE; Lantos PL J Neurol Sci; 1989 Dec; 94(1-3):79-100. PubMed ID: 2559165 [TBL] [Abstract][Full Text] [Related]
11. Glial and neuronal cytoplasmic inclusions in familial olivopontocerebellar atrophy. Berciano J; Ferrer I Ann Neurol; 1996 Nov; 40(5):819-20. PubMed ID: 8957028 [No Abstract] [Full Text] [Related]
12. An autopsy case of early ("minimal change") olivopontocerebellar atrophy (multiple system atrophy-cerebellar). Wakabayashi K; Mori F; Nishie M; Oyama Y; Kurihara A; Yoshimoto M; Kuroda N Acta Neuropathol; 2005 Aug; 110(2):185-90. PubMed ID: 15971057 [TBL] [Abstract][Full Text] [Related]
13. [Peculiar forms of familial olivo-ponto-cerebellar atrophy (Menzel type) and Joseph disease; clinico-neuropathological study of two families with nosological considerations]. Ikeda T Seishin Shinkeigaku Zasshi; 1987; 89(4):245-81. PubMed ID: 3476971 [No Abstract] [Full Text] [Related]
15. Nuclear inclusions in spinocerebellar ataxia type 1. Duyckaerts C; Dürr A; Cancel G; Brice A Acta Neuropathol; 1999 Feb; 97(2):201-7. PubMed ID: 9928833 [TBL] [Abstract][Full Text] [Related]
16. Accumulation of tubular structures in oligodendroglial and neuronal cells as the basic alteration in multiple system atrophy. Papp MI; Lantos PL J Neurol Sci; 1992 Feb; 107(2):172-82. PubMed ID: 1314292 [TBL] [Abstract][Full Text] [Related]
17. Glial cytoplasmic inclusions in multiple system atrophy. Lynch T; Sima AA Ann Neurol; 1996 Mar; 39(3):416. PubMed ID: 8602769 [No Abstract] [Full Text] [Related]
18. [Olivocerebellar atrophy predominantly affecting the vermis (clinical and etiopathogenic aspects apropos of 34 cases)]. Ka M; Kone S; Ndiaye M; Ndiaye IP Dakar Med; 1988; 33(1-4):30-5. PubMed ID: 3079273 [No Abstract] [Full Text] [Related]
19. [Immunohistochemical study of glial cytoplasmic inclusion in multiple system atrophy]. Arai N; Nishimura M; Oda M; Morimatsu Y; Oue R No To Shinkei; 1991 Sep; 43(9):857-62. PubMed ID: 1720637 [TBL] [Abstract][Full Text] [Related]