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Journal Abstract Search

237 related items for PubMed ID: 1232666

  • 21. Progressive myoclonic epilepsy, nerve deafness and spinal muscular atrophy.
    Lance JW, Evans WA.
    Clin Exp Neurol; 1984; 20():141-51. PubMed ID: 6439445
    [Abstract] [Full Text] [Related]

  • 22. [Infantile neuro-axonal dystrophy: anatomo clinical study of one case (author's transl)].
    Onnis L, Nardelli E, Buonanno F, Galiazzo-Rizzuto S, Panizon F, Rizzuto N.
    Riv Patol Nerv Ment; 1975; 96(5):322-39. PubMed ID: 1235007
    [Abstract] [Full Text] [Related]

  • 23. [Dentatorubropallidoluysian atrophy (DRPLA): comparative pathological study on clinical groups classified into juvenile, early adult and late adult types].
    Takeda S, Takahashi H, Ikuta F.
    No To Shinkei; 1992 Feb; 44(2):111-6. PubMed ID: 1567729
    [Abstract] [Full Text] [Related]

  • 24. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
    Iwabuchi K, Kogure T, Oda T, Kato Y, Ohtani K, Endo K, Kosaka K, Amano N, Yagishita S.
    No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
    [Abstract] [Full Text] [Related]

  • 25. Sporadic multi-system atrophy with early onset and rapid fatal outcome (atypical O.P.C.A.?). Case report.
    Barontini F, Marconi GP, Arnetoli G.
    Riv Patol Nerv Ment; 1983 Mar; 104(6):243-54. PubMed ID: 6543985
    [Abstract] [Full Text] [Related]

  • 26. [Myoclonus and epilepsies in children].
    Fejerman N.
    Rev Neurol (Paris); 1991 Mar; 147(12):782-97. PubMed ID: 1780607
    [Abstract] [Full Text] [Related]

  • 27. [A nosological study of a patient showing ataxia & lower motor neuron involvement].
    Murakami N, Yoshida M, Hashizume Y, Muroga T, Takahashi A.
    Rinsho Shinkeigaku; 1989 Sep; 29(9):1116-21. PubMed ID: 2598537
    [Abstract] [Full Text] [Related]

  • 28. [Myoclonic cerebellar dyssynergia (Ramsay Hunt). Description of 2 cases].
    Fryze C, Korwin-Piotrowska T, Potemkowski A, Niezabitowski K.
    Neurol Neurochir Pol; 1985 Sep; 19(6):508-11. PubMed ID: 3835491
    [Abstract] [Full Text] [Related]

  • 29. [A case of juvenile Alzheimer's disease with various neurological features such as myoclonus, showing grumose degeneration in the dentate nucleus].
    Hattori H, Tanaka S, Kondoh H, Nishimura T, Hashimoto S.
    Rinsho Shinkeigaku; 1990 Jun; 30(6):647-53. PubMed ID: 2225661
    [Abstract] [Full Text] [Related]

  • 30. [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]

  • 31. [Acute cerebellar encephalitis in adulthood].
    Kömpf D, Engelhardt A, Dietrich HJ, Neundörfer B.
    Nervenarzt; 1985 Aug; 56(8):431-9. PubMed ID: 4058617
    [Abstract] [Full Text] [Related]

  • 32. [Myoclonic epilepsies].
    Loiseau P.
    Encephale; 1971 Aug; 60(3):245-64. PubMed ID: 5000885
    [No Abstract] [Full Text] [Related]

  • 33. Progressive myoclonus and epilepsy with dentatorubral degeneration: a clinicopathological study of the Ramsay Hunt syndrome.
    Bird TD, Shaw CM.
    J Neurol Neurosurg Psychiatry; 1978 Feb; 41(2):140-9. PubMed ID: 632821
    [Abstract] [Full Text] [Related]

  • 34. [Action myoclonus in Ramsay Hunt myoclonic cerebellar dyssynergyand in Lance-Adams syndrome].
    Tassinari CA, Roger J, Regis H, Sedan R, Lyagoubi S, Gambarelli F, Vallicioni P, Dravet C, Soulayrol R.
    Rev Neurol (Paris); 1970 Nov; 123(5):335-6. PubMed ID: 5513635
    [No Abstract] [Full Text] [Related]

  • 35. [Myoclonal cerebellar dyssynergia].
    Shutov AA, Borodina LG, Zykova TA.
    Vrach Delo; 1985 Jan; (1):102-5. PubMed ID: 3984311
    [No Abstract] [Full Text] [Related]

  • 36. [Myoclonic cerebellar dyssynergia (Ramsay Hunt syndrome)].
    Berciano J, Combarros O.
    Med Clin (Barc); 1986 Jan 18; 86(2):78-82. PubMed ID: 3515066
    [No Abstract] [Full Text] [Related]

  • 37. [An autopsy case of hereditary ataxia (hereditary spastic ataxia)].
    Yagishita S, Nakano T, Iwabuchi K, Sakai H.
    No To Shinkei; 1985 Jun 18; 37(6):603-9. PubMed ID: 4041292
    [Abstract] [Full Text] [Related]

  • 38. Progressive myoclonus epilepsies. Criteria for diagnosis on the basis of the follow-up of 37 cases.
    Guazzi GC, Federico A.
    Acta Neurol (Napoli); 1992 Jun 18; 14(4-6):469-84. PubMed ID: 1293989
    [Abstract] [Full Text] [Related]

  • 39. MRI-based volumetric differentiation of sporadic cerebellar ataxia.
    Burk K, Globas C, Wahl T, Bühring U, Dietz K, Zuhlke C, Luft A, Schulz JB, Voigt K, Dichgans J.
    Brain; 2004 Jan 18; 127(Pt 1):175-81. PubMed ID: 14570820
    [Abstract] [Full Text] [Related]

  • 40. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea].
    Iwabuchi K, Nakazawa Y, Akai J, Yagishita S, Amano N.
    No To Shinkei; 1994 Jun 18; 46(6):563-71. PubMed ID: 8068439
    [Abstract] [Full Text] [Related]

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