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Journal Abstract Search

151 related items for PubMed ID: 2494436

  • 21. [Ramsay-Hunt syndrome and aniridia in 2 monozygotic twins].
    Chazot G, Guard O, Setiey A, Robert JM, Schott B.
    Rev Neurol (Paris); 1975 Jan; 131(1):43-8. PubMed ID: 1080872
    [No Abstract] [Full Text] [Related]

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

  • 23. Hereditary spino-cerebellar degeneration and Ramsay-Hunt disease.
    Penneau D, Bigorgne JC, Fressinaud-Masdefeix L.
    Cah Med; 1974 Feb; 15(2):93-6. PubMed ID: 4848865
    [No Abstract] [Full Text] [Related]

  • 24. [A case of dyssynergia cerebellaris myoclonica (Ramsay-Hunt syndrome)].
    Cemalović-Boko Z, Hajnsek F.
    Neurologija; 1983 Feb; 31(1-2):63-74. PubMed ID: 6679060
    [No Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. 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]

  • 27. [Electroencephalographic study of myoclonic cerebellar dyssynergia with epilepsy (Ramsay-Hunt syndrome)].
    Tassinari CA, Bureau-Paillas M, Grasso E, Roger J.
    Rev Electroencephalogr Neurophysiol Clin; 1974 Oct; 4(3):407-28. PubMed ID: 4470962
    [No Abstract] [Full Text] [Related]

  • 28. [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]

  • 29. [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]

  • 30. [Generalized status epilepticus of confusional manifestation in a patient with Ramsay Hunt myoclonic cerebellar dyssynergia].
    Mazza S, Ferro FM, Bergonzi P.
    Riv Neurol; 1976 Nov; 46(6):508-14. PubMed ID: 1013612
    [No Abstract] [Full Text] [Related]

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  • 32. [Ramsay Hunt syndrome].
    Fukuda I, Yoshida T, Mozai T.
    Nihon Rinsho; 1977 Nov; 35 Suppl 1():1284-5. PubMed ID: 612821
    [No Abstract] [Full Text] [Related]

  • 33. What is it? Case 2, 1986.
    Mov Disord; 1986 Nov; 1(4):281-7. PubMed ID: 3504252
    [No Abstract] [Full Text] [Related]

  • 34. [Myoclonic cerebellar dyssynergia. Clinico-tomographic and cisternographic study of a case].
    Tessitore A, Battaglia A, Aprile A.
    Acta Neurol Quad (Napoli); 1981 Nov; 42():47-50. PubMed ID: 7270077
    [No Abstract] [Full Text] [Related]

  • 35. Oculomotor abnormalities in Dyssynergia cerebellaris myoclonica.
    Wiest G, Mueller C, Wessely P, Steinhoff N, Trattnig S, Deecke L.
    Acta Otolaryngol Suppl; 1995 Nov; 520 Pt 2():392-4. PubMed ID: 8749170
    [Abstract] [Full Text] [Related]

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  • 38. Cerebellar ataxia and gluten sensitivity: a rare but possible cause of ataxia, even in childhood.
    Gordon N.
    Dev Med Child Neurol; 2000 Apr; 42(4):283-6. PubMed ID: 10795570
    [No Abstract] [Full Text] [Related]

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