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Journal Abstract Search

177 related items for PubMed ID: 4267723

  • 1. [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]

  • 2. [Genetic aspects of some spino-cerebellar degenerations].
    Badiu G.
    Stud Cercet Neurol; 1969 Jan; 14(5):311-24. PubMed ID: 4906012
    [No Abstract] [Full Text] [Related]

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

  • 4. 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]

  • 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. [Amyotrophic form of a spinocerebellar degeneration. Anatomoclinical study and nosological discussion].
    Boudouresques J, Toga M, Khalil R, Gosset A, Vigouroux RA, Pellissier JF.
    Rev Neurol (Paris); 1971 Jul; 125(1):25-38. PubMed ID: 5138162
    [No Abstract] [Full Text] [Related]

  • 7. [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]

  • 8. [The two siblings of Friedreich's ataxia with proximal neurogenic muscular atrophy (author's transl)].
    Ikeda S, Hanyu N, Oguchi K, Yanagisawa N, Tsukagoshi H.
    Rinsho Shinkeigaku; 1980 Apr; 20(4):280-5. PubMed ID: 7408332
    [No Abstract] [Full Text] [Related]

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

  • 10. [Spinocerebellar syndrome of early onset associated with retinal degeneration. Report of a case].
    Onsurbe Ramírez I, Lorenzo Sanz G, Aparicio Meix JM.
    An Esp Pediatr; 1990 Oct; 33(4):387-9. PubMed ID: 2278445
    [No Abstract] [Full Text] [Related]

  • 11. [Progressive supranuclear palsy with familial occurrence of spinocerebellar degeneration].
    Yamamura Y, Kito S, Itoga E, Kajiwara H.
    Rinsho Shinkeigaku; 1982 Jul; 22(7):586-93. PubMed ID: 7172528
    [No Abstract] [Full Text] [Related]

  • 12. [Retinal degeneration and ophthalmoplegia associated with hereditary cerebellar ataxia].
    De Marco P.
    Riv Patol Nerv Ment; 1968 Feb; 89(1):34-46. PubMed ID: 5760400
    [No Abstract] [Full Text] [Related]

  • 13. [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 Feb; 39():77-89. PubMed ID: 555248
    [No Abstract] [Full Text] [Related]

  • 14. [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]

  • 15. Neurological syndromes associated with pes cavus.
    Heron JR.
    Proc R Soc Med; 1969 Mar 03; 62(3):270-1. PubMed ID: 4181287
    [No Abstract] [Full Text] [Related]

  • 16. [Insulin availability in some familial inherited neurological syndromes (author's transl)].
    Fratino P, Kauchtschischvili G, Nappi G, Poloni M, Favino A, Criffò A.
    Riv Patol Nerv Ment; 1974 Oct 03; 95(5):624-31. PubMed ID: 4283420
    [No Abstract] [Full Text] [Related]

  • 17. [Heredoataxia and tapetoretinal degeneration (genetic relation)].
    Boyazis RM, Hariga J, Myle G.
    Encephale; 1968 Oct 03; 57(6):495-514. PubMed ID: 5730656
    [No Abstract] [Full Text] [Related]

  • 18. [Hereditary association of tapeto-retinal dystrophy, retinitis punctata albescens, with spinal-cerebellar Friedreich's ataxia].
    Travkin AG, Basis VIu, Aladinskaia LV, Kunicheva GS.
    Vestn Oftalmol; 1975 Oct 03; (3):84-7. PubMed ID: 1154603
    [No Abstract] [Full Text] [Related]

  • 19. Association of Friedreich's ataxia and peroneal muscular atrophy (familial ataxia with atrophy). Report of two cases.
    Chopra JS, Dutta AK, Bawa YS.
    J Assoc Physicians India; 1969 Feb 03; 17(2):123-6. PubMed ID: 5346505
    [No Abstract] [Full Text] [Related]

  • 20. [Marie's ataxia with nuclear external ophthalmoplegia and muscle atrophy of lower extremities--report of an autopsy case and its family (author's transl)].
    Kurachi M, Shibata T, Koyama Y, Isaki K, Yamaguchi N.
    Seishin Shinkeigaku Zasshi; 1977 Feb 03; 79(1):1-25. PubMed ID: 577311
    [No Abstract] [Full Text] [Related]

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