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PUBMED FOR HANDHELDS

Journal Abstract Search


175 related items for PubMed ID: 5001029

  • 21. [Clinico-electromyographic characteristics of movement disorders during seizures in epileptic patients].
    Beliaev IuI, Klushin DF.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(11):1658-62. PubMed ID: 4204936
    [No Abstract] [Full Text] [Related]

  • 22. Photosensitivity--genetics and clinical significance.
    Doose H, Waltz S.
    Neuropediatrics; 1993 Oct; 24(5):249-55. PubMed ID: 8309513
    [Abstract] [Full Text] [Related]

  • 23. [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]

  • 24. Genetic factors in spike-wave absences.
    Doose H, Gerken H, Horstmann T, Völzke E.
    Epilepsia; 1973 Mar; 14(1):57-75. PubMed ID: 4200260
    [No Abstract] [Full Text] [Related]

  • 25. Photosensitivity in epileptic syndromes of childhood and adolescence.
    Lu Y, Waltz S, Stenzel K, Muhle H, Stephani U.
    Epileptic Disord; 2008 Jun; 10(2):136-43. PubMed ID: 18539564
    [Abstract] [Full Text] [Related]

  • 26. [Influence of alcohol on photomyoclomus and photoconvulsive response (author's transl)].
    Klingler D, Wessely P.
    EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb; 1976 Jun; 7(2):81-6. PubMed ID: 829052
    [Abstract] [Full Text] [Related]

  • 27. Childhood absence epilepsy evolving to juvenile myoclonic epilepsy: electroclinical and genetic features.
    Medina MT, Durón RM, Alonso ME, Dravet C, León L, López-Ruiz M, Ramos-Ramírez R, Castroviejo IP, Weissbecker K, Westling B, Perez-Gosiengfiao KT, Khan S, Pineda G, Morita R, Rasmussen A, Peek JR, Cordova S, Martínez-Juárez IE, Rubio-Donnadieu F, Ochoa-Morales A, Jara-Prado A, Bailey JN, Tanaka M, Bai D, Machado-Salas J, Delgado-Escueta AV.
    Adv Neurol; 2005 Jun; 95():197-215. PubMed ID: 15508924
    [No Abstract] [Full Text] [Related]

  • 28. The clinical significance of spike and wave abnormalities in the adult.
    Crews J, Sidell AD.
    Bull Los Angeles Neurol Soc; 1973 Apr; 38(2):60-8. PubMed ID: 4634004
    [No Abstract] [Full Text] [Related]

  • 29. "Benign" or "functional" (versus "organic") epilepsies in different stages of life: an analysis of the corresponding age-related variations in the predisposition to epilepsy.
    Gastaut H.
    Electroencephalogr Clin Neurophysiol Suppl; 1982 Apr; (35):17-44. PubMed ID: 6811248
    [No Abstract] [Full Text] [Related]

  • 30. [Editorial: epilepsy].
    Gastaut H, Roger J, Tassinari CA.
    Afr J Med Sci; 1970 Apr; 1(2):115-23. PubMed ID: 5000528
    [No Abstract] [Full Text] [Related]

  • 31. Genetics of photosensitive epilepsy.
    Doose H, Gerken H, Hien-Völpel KF, Völzke E.
    Neuropadiatrie; 1969 Apr; 1(1):56-73. PubMed ID: 5409292
    [No Abstract] [Full Text] [Related]

  • 32. [Diagnostic focus on the child with myoclonic seizures in isolation or associated with other types of seizures].
    Herranz JL, de las Cuevas I.
    Rev Neurol; 1998 Feb; 26(150):301-7. PubMed ID: 9563099
    [Abstract] [Full Text] [Related]

  • 33. [Epileptic seizures and myoclonus in kidney failure].
    Karbowski K, Wegmüller E.
    Schweiz Rundsch Med Prax; 1983 Jun 14; 72(24):832-9. PubMed ID: 6410367
    [No Abstract] [Full Text] [Related]

  • 34. Eyelid myoclonia with absences (Jeavons syndrome): a well-defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions?
    Striano S, Capovilla G, Sofia V, Romeo A, Rubboli G, Striano P, Trenité DK.
    Epilepsia; 2009 May 14; 50 Suppl 5():15-9. PubMed ID: 19469840
    [Abstract] [Full Text] [Related]

  • 35. [Dyssynergia cerebellaris myoclonica Hunt].
    Tieber E, Schenck K.
    Neuropadiatrie; 1970 Apr 14; 1(4):461-8. PubMed ID: 5538084
    [No Abstract] [Full Text] [Related]

  • 36. [Clinical and EEG studies in children of epileptics (author's transl)].
    Christiani K.
    Fortschr Neurol Psychiatr Grenzgeb; 1979 May 14; 47(5):221-63. PubMed ID: 256553
    [No Abstract] [Full Text] [Related]

  • 37. On the genetics of EEG-anomalies in childhood. IV. Photoconvulsive reaction.
    Doose H, Gerken H.
    Neuropadiatrie; 1973 Apr 14; 4(2):162-71. PubMed ID: 4740439
    [No Abstract] [Full Text] [Related]

  • 38. [Siblings with myoclonus corpuscle disease (Unverricht-Lundborg). Family and longitudinal section study].
    Barolin GS, Pateisky K.
    Wien Z Nervenheilkd Grenzgeb; 1969 Apr 14; 27(1):1-8. PubMed ID: 4241179
    [No Abstract] [Full Text] [Related]

  • 39. The prognosis of seizures in the first three years of life.
    Brett EM.
    Mod Trends Neurol; 1975 Apr 14; 6():303-19. PubMed ID: 811972
    [No Abstract] [Full Text] [Related]

  • 40. Spectrum of epilepsy in terminal 1p36 deletion syndrome.
    Bahi-Buisson N, Guttierrez-Delicado E, Soufflet C, Rio M, Daire VC, Lacombe D, Héron D, Verloes A, Zuberi S, Burglen L, Afenjar A, Moutard ML, Edery P, Novelli A, Bernardini L, Dulac O, Nabbout R, Plouin P, Battaglia A.
    Epilepsia; 2008 Mar 14; 49(3):509-15. PubMed ID: 18031548
    [Abstract] [Full Text] [Related]


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