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Journal Abstract Search

112 related items for PubMed ID: 5748751

  • 1. Hereditary muscular atrophy with ataxia, retinitis pigmentosa, and diabetes mellitus. A clinical report of a family.
    Furukawa T, Takagi A, Nakao K, Sugita H, Tsukagoshi H.
    Neurology; 1968 Oct; 18(10):942-7. PubMed ID: 5748751
    [No Abstract] [Full Text] [Related]

  • 2. [Electroretinography and electroencephalography in spinocerebellar degenerations].
    Stanescu B, Wawernia E.
    Arch Ophtalmol Rev Gen Ophtalmol; 1973 Jan; 33(1):43-8. PubMed ID: 4267723
    [No Abstract] [Full Text] [Related]

  • 3. [Ophthalmoplegia plus: clinical, metabolic and histochemical study of a new case].
    Cotrufo R, Di Iorio G, Aguglia U, Cotticelli L, D'Auria N, Bonavita V.
    Acta Neurol Quad (Napoli); 1979 Jan; 39():77-89. PubMed ID: 555248
    [No Abstract] [Full Text] [Related]

  • 4. [Hereditary cerebellar aataxia with spinal muscular atrophies].
    Hopf HC, Duensing F, Lowitzsch K, Krönke R.
    Z Neurol; 1971 Jan; 199(4):344-52. PubMed ID: 4104837
    [No Abstract] [Full Text] [Related]

  • 5. [Nosology of Von Graefe-Lindenov syndrome. Study of mental disorders in this genetic neurosensory disease].
    Nehlil J.
    Ann Med Psychol (Paris); 1981 Mar; 139(3):352-6. PubMed ID: 7325492
    [No Abstract] [Full Text] [Related]

  • 6. [Retinitis pigmentosa with congenital deaf-mutism and cerebellar heredoataxia].
    Stefănescu Dima A.
    Rev Chir Oncol Radiol O R L Oftalmol Stomatol Ser Oftalmol; 1982 Mar; 26(3):231-5. PubMed ID: 6218541
    [No Abstract] [Full Text] [Related]

  • 7. Late onset ataxia, rigidity, and peripheral neuropathy. A familial syndrome with variable therapeutic response to levodopa.
    Ziegler DK, Schimke RN, Kepes JJ, Rose DL, Klinkerfuss G.
    Arch Neurol; 1972 Jul; 27(1):52-66. PubMed ID: 4340377
    [No Abstract] [Full Text] [Related]

  • 8. [A case of spinocerebellar ataxia with retinitis pigmentosa, deafness, seizure and EEG abnormality (author's transl)].
    Itoh J, Akiguchi I, Tanaka M, Nakamura S, Kameyama M.
    Rinsho Shinkeigaku; 1980 Jul; 20(7):577-83. PubMed ID: 7460428
    [No Abstract] [Full Text] [Related]

  • 9. Genetic and epidemiological investigations on pigmentary degeneration of the retina and allied disorders in Switzerland.
    Ammann F, Klein D, Franceschetti A.
    J Neurol Sci; 1965 Jul; 2(2):183-96. PubMed ID: 5878602
    [No Abstract] [Full Text] [Related]

  • 10. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.
    Benomar A, Le Guern E, Dürr A, Ouhabi H, Stevanin G, Yahyaoui M, Chkili T, Agid Y, Brice A.
    Ann Neurol; 1994 Apr; 35(4):439-44. PubMed ID: 8154871
    [Abstract] [Full Text] [Related]

  • 11. The clinical incidence of myoclonus.
    Halliday AM.
    Mod Trends Neurol; 1967 Apr; 4(0):69-105. PubMed ID: 4277685
    [No Abstract] [Full Text] [Related]

  • 12. [Hereditary motor and sensory neuropathy associated with retinitis pigmentosa and neural deafness].
    Murakami K, Sobue G, Takahashi A, Mitsuma T.
    Rinsho Shinkeigaku; 1986 Sep; 26(9):952-9. PubMed ID: 3791775
    [No Abstract] [Full Text] [Related]

  • 13. [A family with progressive neural muscular atrophy--with special reference to relation with allied diseases (author's transl)].
    Hayashi Y, Tomita M, Shimizu K, Takamiya M, Watanabe H.
    Rinsho Shinkeigaku; 1978 Oct; 18(10):593-600. PubMed ID: 709963
    [No Abstract] [Full Text] [Related]

  • 14. [Mitochondrial encephalomyopathy with retinitis pigmentosa, cataract, deafness, ataxia and dementia--a case report].
    Yamamoto M, Wada Y, Sano M, Furukawa T, Tsukagoshi H.
    Rinsho Shinkeigaku; 1986 Oct; 26(10):1080-7. PubMed ID: 3802662
    [No Abstract] [Full Text] [Related]

  • 15. [Ataxia associated with pyramidal tract diseases].
    Nogi K, Tsuchida T.
    Nihon Rinsho; 1971 Aug; 29(8):1870-7. PubMed ID: 5170137
    [No Abstract] [Full Text] [Related]

  • 16. Ocular myopathy.
    Davidson SI.
    Trans Ophthalmol Soc U K (1962); 1970 Aug; 90():139-59. PubMed ID: 4933925
    [No Abstract] [Full Text] [Related]

  • 17. [OLIGOPHRENIA, CONGENITAL CATARACT, RETINITIS PIGMENTOSA, CEREBELLAR ATAXIA, NEUROGENIC AMYOTROPHIA. OBSERVATIONS ON 3 FAMILIAL CASES AND COMPARISON WITH THE MARINESCO-SJOGREN'S SYNDROME].
    CALVI LA.
    Sist Nerv; 1963 Aug; 15():189-98. PubMed ID: 14073896
    [No Abstract] [Full Text] [Related]

  • 18. A patient homozygous for the SCA6 gene with retinitis pigmentosa.
    Fukutake T, Kamitsukasa I, Arai K, Hattori T, Nakajima T.
    Clin Genet; 2002 May; 61(5):375-9. PubMed ID: 12081723
    [Abstract] [Full Text] [Related]

  • 19. Machado disease. A hereditary ataxia in Portuguese emigrants to Massachusetts.
    Nakano KK, Dawson DM, Spence A.
    Neurology; 1972 Jan; 22(1):49-55. PubMed ID: 5061839
    [No Abstract] [Full Text] [Related]

  • 20. Hereditary spastic paraplegia in Western Norway.
    Skre H.
    Clin Genet; 1974 Jan; 6(3):165-83. PubMed ID: 4426134
    [No Abstract] [Full Text] [Related]

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