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Journal Abstract Search

142 related items for PubMed ID: 2812335

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. [Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)].
    Iwabuchi K, Kosaka K, Haga C, Tuchiya K, Amano N, Itoh K, Yagishita S, Mizutani Y.
    No To Shinkei; 1991 Jun; 43(6):561-8. PubMed ID: 1654964
    [Abstract] [Full Text] [Related]

  • 23. Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.
    Harding BN, Dunger DB, Grant DB, Erdohazi M.
    J Neurol Neurosurg Psychiatry; 1988 Mar; 51(3):385-90. PubMed ID: 3162953
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Changes in vitamin E concentration in red blood cells and plasma of patients with olivopontocerebellar ataxia within the Schut-Swier kindred.
    Vatassery GT, Schut LJ.
    J Am Coll Nutr; 1987 Apr; 6(2):151-6. PubMed ID: 3473124
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Hereditary ataxia.
    Rosenberg RN, Grossman A.
    Neurol Clin; 1989 Feb; 7(1):25-36. PubMed ID: 2564162
    [Abstract] [Full Text] [Related]

  • 28. Olivopontocerebellar atrophy.
    Choi IS, Lee MS, Kim WT, Choi KK.
    Yonsei Med J; 1988 Feb; 29(3):233-8. PubMed ID: 3195154
    [No Abstract] [Full Text] [Related]

  • 29. [Linkage study of hereditary olivopontocerebellar atrophy: genetic evidence for locus heterogeneity in Japanese cases].
    Sasaki H, Wakisaka A, Tashiro K, Hamada T, Shima K.
    Rinsho Shinkeigaku; 1992 Jan; 32(1):17-22. PubMed ID: 1628432
    [Abstract] [Full Text] [Related]

  • 30. [Clinical study of gene locus heterogeneity in hereditary olivopontocerebellar atrophy (OPCA)--report of 2 pedigrees affected with non SCA1 type OPCA].
    Sasaki H, Wakisaka A, Tashiro K, Hamada T, Shima K.
    Rinsho Shinkeigaku; 1991 Nov; 31(11):1170-6. PubMed ID: 1813183
    [Abstract] [Full Text] [Related]

  • 31. Brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophy.
    Kish SJ, Currier RD, Schut L, Perry TL, Morito CL.
    Ann Neurol; 1987 Aug; 22(2):272-5. PubMed ID: 3477997
    [Abstract] [Full Text] [Related]

  • 32. Wadia type olivopontocerebellar degeneration: a case history and review of literature.
    Washington C, Gore E.
    J Miss State Med Assoc; 1991 Jul; 32(7):255-7. PubMed ID: 1658328
    [Abstract] [Full Text] [Related]

  • 33. Cerebellar and brainstem hypometabolism in olivopontocerebellar atrophy detected with positron emission tomography.
    Gilman S, Markel DS, Koeppe RA, Junck L, Kluin KJ, Gebarski SS, Hichwa RD.
    Ann Neurol; 1988 Mar; 23(3):223-30. PubMed ID: 3259853
    [Abstract] [Full Text] [Related]

  • 34. Electroencephalographic findings of hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
    Inazuki G, Baba K, Naito H.
    Jpn J Psychiatry Neurol; 1989 Jun; 43(2):213-20. PubMed ID: 2529387
    [Abstract] [Full Text] [Related]

  • 35. Olivopontocerebellar atrophy with retinal degeneration. An electroretinographic and histopathologic investigation.
    To KW, Adamian M, Jakobiec FA, Berson EL.
    Ophthalmology; 1993 Jan; 100(1):15-23. PubMed ID: 8433819
    [Abstract] [Full Text] [Related]

  • 36. [Olivopontocerebellar atrophy associated with nigrostriatal degeneration].
    Ricart C, Lamarca J, Balaguer E, Fossas P.
    Rev Clin Esp; 1986 Nov; 179(8):432-3. PubMed ID: 3470856
    [No Abstract] [Full Text] [Related]

  • 37. [A family with Menzel's disease showing dementia and various extrapyramidal symptoms].
    Iwabuchi K, Nagatomo H, Tanabe T, Oda T, Itoh H, Hanihara T, Yagishita S.
    No To Shinkei; 1993 Sep; 45(9):841-9. PubMed ID: 8217410
    [Abstract] [Full Text] [Related]

  • 38. 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
    [Abstract] [Full Text] [Related]

  • 39. Olivopontocerebellar atrophy with retinal degeneration. A clinical and ocular histopathologic study.
    Traboulsi EI, Maumenee IH, Green WR, Freimer ML, Moser H.
    Arch Ophthalmol; 1988 Jun; 106(6):801-6. PubMed ID: 3163477
    [Abstract] [Full Text] [Related]

  • 40. Low leukocyte glutamate dehydrogenase activity does not correlate with a particular type of multiple system atrophy.
    Duvoisin RC, Nicklas WJ, Ritchie V, Sage J, Chokroverty S.
    J Neurol Neurosurg Psychiatry; 1988 Dec; 51(12):1508-11. PubMed ID: 3221218
    [Abstract] [Full Text] [Related]

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