BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 6388270)

  • 21. Progressive ataxia, palatal tremor, and the Romberg sign.
    Teive HA; Munhoz RP
    Arch Neurol; 2009 Feb; 66(2):284-5; author reply 285. PubMed ID: 19204175
    [No Abstract]   [Full Text] [Related]  

  • 22. The olivopontocerebellar atrophies.
    Adv Neurol; 1984; 41():1-286. PubMed ID: 6496223
    [No Abstract]   [Full Text] [Related]  

  • 23. Clinical features of sporadic (Dejerine-Thomas) olivopontocerebellar atrophy.
    Caplan LR
    Adv Neurol; 1984; 41():217-24. PubMed ID: 6496227
    [No Abstract]   [Full Text] [Related]  

  • 24. [Olivo-ponto-cerebellar atrophy with olivary hypertrophy, binucleated neurons and fibrous gliosis in the cerebral white matter (author's transl)].
    Tateishi J; Masuda T; Ohmura I; Kirimoto T
    No To Shinkei; 1979 May; 31(5):523-8. PubMed ID: 486270
    [No Abstract]   [Full Text] [Related]  

  • 25. Olivopontocerebellar atrophy. A review of 117 cases.
    Berciano J
    J Neurol Sci; 1982 Feb; 53(2):253-72. PubMed ID: 7057212
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [An autopsy case of olivopontocerebellar atrophy clinically manifested by parkinsonism and not accompanied by marked cerebellar ataxia throughout the course (author's transl)].
    Yamamura Y; Kito S; Araki S; Terao A; Akamizu H
    Rinsho Shinkeigaku; 1981 Aug; 21(8):682-90. PubMed ID: 7326888
    [No Abstract]   [Full Text] [Related]  

  • 27. An apology and an introduction to the olivopontocerebellar atrophies.
    Duvoisin RC
    Adv Neurol; 1984; 41():5-12. PubMed ID: 6496230
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through six generations.
    Weiner LP; Konigsmark BW; Stoll J; Magladery JW
    Arch Neurol; 1967 Apr; 16(4):364-76. PubMed ID: 6021917
    [No Abstract]   [Full Text] [Related]  

  • 29. [Olivo-ponto-cerebellar atrophy with personality changes and slight disturbance of intelligence].
    Deshimaru M; Miyakawa T; Suzuki T
    No To Shinkei; 1976 Dec; 28(12):1297-302. PubMed ID: 1036031
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Neuroradiologic and neurophysiologic studies in patients with olivo-ponto-cerebellar atrophy].
    Rossi L; Zappoli F; De Scisciolo G; Bindi A; Costantini S; Amantini A; Ronchi O; Pagnini P; Marini P; Zappoli R
    Riv Neurobiol; 1984; 30(2-3):575-89. PubMed ID: 6544507
    [No Abstract]   [Full Text] [Related]  

  • 31. Progression of the olivopontocerebellar form of adrenoleukodystrophy as shown by MRI.
    Suda S; Komaba Y; Kumagai T; Yamazaki M; Katsumata T; Kamiya T; Katayama Y
    Neurology; 2006 Jan; 66(1):144-5. PubMed ID: 16401870
    [No Abstract]   [Full Text] [Related]  

  • 32. Reduction of noradrenaline in cerebellum of patients with olivopontocerebellar atrophy.
    Kish SJ; Shannak KS; Hornykiewicz O
    J Neurochem; 1984 May; 42(5):1476-8. PubMed ID: 6707646
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Morphological changes of olivopontocerebellar atrophy in computed tomography and comments on its pathogenesis.
    Huang YP; Plaitakis A
    Adv Neurol; 1984; 41():39-85. PubMed ID: 6496229
    [No Abstract]   [Full Text] [Related]  

  • 34. Menzel's hereditary ataxia with slow eye movements and myoclonus. A clinico-pathological study.
    Rondot P; De Recondo J; Davous P; Vedrenne C
    J Neurol Sci; 1983 Sep; 61(1):65-80. PubMed ID: 6631453
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Cerebellar atrophies].
    Escourolle R; Gray F; Hauw JJ
    Rev Neurol (Paris); 1982; 138(12):953-65. PubMed ID: 6763297
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Lysosomes and lysosomal enzymes in the central nervous system (author's transl)].
    Davidoff MS; Galabov GP
    Prog Histochem Cytochem; 1974; 6(2):1-64. PubMed ID: 4457953
    [No Abstract]   [Full Text] [Related]  

  • 37. Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN
    Adv Neurol; 1984; 41():179-93. PubMed ID: 6388271
    [No Abstract]   [Full Text] [Related]  

  • 38. [A case of olivo-ponto-cerebellar atrophy (OPCA) with unique gait disturbance. Possible role of reciprocal excitation].
    Neshige R; Oda K; Shibasaki H
    Rinsho Shinkeigaku; 1984 Mar; 24(3):307-12. PubMed ID: 6467750
    [No Abstract]   [Full Text] [Related]  

  • 39. Four biochemically different types of dominantly inherited olivopontocerebellar atrophy.
    Perry TL
    Adv Neurol; 1984; 41():205-16. PubMed ID: 6149676
    [No Abstract]   [Full Text] [Related]  

  • 40. [The clinical picture of olivo-ponto-cerebellar atrophy (Déjérine-Thomas)].
    Kulawik H; Roitzsch E; Barz H
    Psychiatr Neurol Med Psychol (Leipz); 1972 Mar; 24(3):119-27. PubMed ID: 5034933
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.