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Journal Abstract Search

230 related items for PubMed ID: 1336290

  • 1. Progressive myoclonic ataxia without ragged red fibres: Unverricht-Lundborg disease vs Ramsay Hunt syndrome.
    Shakir RA, Khan RA, al-Zuhair AG.
    Acta Neurol Scand; 1992 Nov; 86(5):470-3. PubMed ID: 1336290
    [Abstract] [Full Text] [Related]

  • 2. Progressive myoclonic ataxia (the Ramsay Hunt syndrome).
    Marsden CD, Harding AE, Obeso JA, Lu CS.
    Arch Neurol; 1990 Oct; 47(10):1121-5. PubMed ID: 2121121
    [Abstract] [Full Text] [Related]

  • 3. Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
    Harding AE.
    Mov Disord; 1989 Oct; 4(1):18-9. PubMed ID: 2494437
    [No Abstract] [Full Text] [Related]

  • 4. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes.
    Lance JW.
    Adv Neurol; 1986 Oct; 43():33-55. PubMed ID: 3080851
    [Abstract] [Full Text] [Related]

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

  • 6. [Progressive myoclonus epilepsy in two siblings and 5 cases with dyssynergia cerebellaris myoclonica in several generations of a kinship, a clinical and genetic study].
    Diebold K, Kastner M, Penin H.
    Nervenarzt; 1974 Nov; 45(11):595-601. PubMed ID: 4217888
    [No Abstract] [Full Text] [Related]

  • 7. Sleep abnormalities in four cases of dyssynergia cerebellaris myoclonica of Ramsay-Hunt.
    Benassi E, Abbruzzese M, Ottonello GA, Tanganelli P.
    Ital J Neurol Sci; 1981 May; 2(2):159-63. PubMed ID: 6800975
    [Abstract] [Full Text] [Related]

  • 8. The Ramsay Hunt syndrome revisited: Mediterranean myoclonus versus mitochondrial encephalomyopathy with ragged-red fibers and Baltic myoclonus.
    Genton P, Michelucci R, Tassinari CA, Roger J.
    Acta Neurol Scand; 1990 Jan; 81(1):8-15. PubMed ID: 2109922
    [Abstract] [Full Text] [Related]

  • 9. Ramsay Hunt syndrome: New impressions in the era of molecular genetics.
    Teive HAG, Cassou E, Coutinho L, Camargo CHF, Munhoz RP.
    Parkinsonism Relat Disord; 2022 Apr; 97():101-104. PubMed ID: 35430109
    [Abstract] [Full Text] [Related]

  • 10. Ramsay Hunt syndrome: progressive mental deterioration in association with unusual cerebral white matter change.
    Kobayashi K, Morikawa K, Fukutani Y, Miyazu K, Nakamura I, Yamaguchi N, Watanabe H.
    Clin Neuropathol; 1994 Apr; 13(2):88-96. PubMed ID: 8205732
    [Abstract] [Full Text] [Related]

  • 11. [Spinocerebellar degeneration, optic atrophy, epilepsy, myoclonus and mitochondrial myopathy: a case report (author's transl)].
    Roger J, Pellissier JF, Dravet C, Bureau-Paillas M, Arnoux M, Larrieu JL.
    Rev Neurol (Paris); 1982 Apr; 138(3):187-200. PubMed ID: 6810437
    [Abstract] [Full Text] [Related]

  • 12. Genetic transmission of myoclonus epilepsy with ragged red fibers.
    Roger J.
    Ann Neurol; 1986 Oct; 20(4):545-6. PubMed ID: 3098158
    [No Abstract] [Full Text] [Related]

  • 13. Mitochondrial myopathy and lactic acidaemia with myoclonic epilepsy, ataxia and hypothalamic infertility: a variant of Ramsay-Hunt syndrome?
    Fitzsimons RB, Clifton-Bligh P, Wolfenden WH.
    J Neurol Neurosurg Psychiatry; 1981 Jan; 44(1):79-82. PubMed ID: 6782198
    [Abstract] [Full Text] [Related]

  • 14. The Ramsay Hunt syndrome is no longer a useful diagnostic category.
    Andermann F, Berkovic S, Carpenter S, Andermann E.
    Mov Disord; 1989 Jan; 4(1):13-7. PubMed ID: 2494436
    [No Abstract] [Full Text] [Related]

  • 15. [Unverricht-Lundborg myoclonic epilepsy in 3 siblings].
    Jezierska K, Nawrocka I.
    Neurol Neurochir Pol; 1971 Jan; 5(2):241-4. PubMed ID: 4252636
    [No Abstract] [Full Text] [Related]

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

  • 17. A clinical analysis of myoclonus epilepsy (Unverricht-Lundborg), myoclonic cerebellar dyssynergy (Hunt) and hepatolenticular degeneration (Wilson).
    WOHLFART G, HOOK O.
    Acta Psychiatr Neurol Scand; 1951 Jan; 26(2):219-45. PubMed ID: 14902532
    [No Abstract] [Full Text] [Related]

  • 18. Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 cases.
    Franceschetti S, Antozzi C, Binelli S, Carrara F, Nardocci N, Zeviani M, Avanzini G.
    Acta Neurol Scand; 1993 Mar; 87(3):219-23. PubMed ID: 8386419
    [Abstract] [Full Text] [Related]

  • 19. [The relationship of dyssynergia cerebellaris myoclonica (Hunt) to myoclonus epilepsy (Unverricht-Lundborg)].
    SEITZ D.
    Dtsch Z Nervenheilkd; 1955 Mar; 173(2):111-22. PubMed ID: 14391125
    [No Abstract] [Full Text] [Related]

  • 20. Differential diagnosis of familial adult myoclonic epilepsy.
    Baykan B, Franceschetti S, Canafoglia L, Cavalleri GL, Michelucci R, Scheffer IE.
    Epilepsia; 2023 Jun; 64 Suppl 1():S52-S57. PubMed ID: 36751956
    [Abstract] [Full Text] [Related]

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