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Journal Abstract Search

113 related items for PubMed ID: 4252636

  • 41. [Progressive familial myoclonic epilepsy (Unverricht-Lundborg syndrome). Genetic, clinical, polygraphic and histopathologic findings].
    Giuliani G, Marchesi GF, Quattrini A, Jezequel AM, Koch M, Pace DP.
    Minerva Med; 1977 Sep 15; 68(42):2923-54. PubMed ID: 198702
    [No Abstract] [Full Text] [Related]

  • 42. Severer phenotype in Unverricht-Lundborg disease (EPM1) patients compound heterozygous for the dodecamer repeat expansion and the c.202C>T mutation in the CSTB gene.
    Koskenkorva P, Hyppönen J, Aikiä M, Mervaala E, Kiviranta T, Eriksson K, Lehesjoki AE, Vanninen R, Kälviäinen R.
    Neurodegener Dis; 2011 Sep 15; 8(6):515-22. PubMed ID: 21757863
    [Abstract] [Full Text] [Related]

  • 43. Comparative anticonvulsant effect of several Librium analogs.
    Pomina AC, Tarlau M, Berman AJ.
    Electroencephalogr Clin Neurophysiol; 1967 Jul 15; 23(1):96. PubMed ID: 4165623
    [No Abstract] [Full Text] [Related]

  • 44. [MYOCLONIC EPILEPSY OF THE UNVERRICHT-LUNDBORG TYPE. CLINICAL, ELECTROENCEPHALOGRAPHIC AND ELECTROMYOGRAPHIC STUDY OF A CASE].
    MARTINO P, BERT J, ZWINGELSTEIN J, COLLOMB H.
    Bull Soc Med Afr Noire Lang Fr; 1964 Jul 15; 9():181-6. PubMed ID: 14276620
    [No Abstract] [Full Text] [Related]

  • 45. Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration.
    Hirvasniemi A, Lang H, Lehesjoki AE, Leisti J.
    J Med Genet; 1994 Mar 15; 31(3):177-82. PubMed ID: 8014963
    [Abstract] [Full Text] [Related]

  • 46. Lamotrigine adjunctive therapy among children and adolescents with primary generalized tonic-clonic seizures.
    Trevathan E, Kerls SP, Hammer AE, Vuong A, Messenheimer JA.
    Pediatrics; 2006 Aug 15; 118(2):e371-8. PubMed ID: 16847080
    [Abstract] [Full Text] [Related]

  • 47. [Epilepsy, physiopathological course in relation to age].
    Adams RD, Salam MZ.
    Schweiz Med Wochenschr; 1967 Dec 23; 97(51):1707-16. PubMed ID: 4968315
    [No Abstract] [Full Text] [Related]

  • 48. [Mode of inheritance of idiopathic generalized non-myoclonic epilepsy in families investigated by studying members with idiopathic epilepsy with tonic-clonic crises on waking. Antioquia, Colombia].
    Mora O, Jiménez I, Palacio LG, Jiménez M, Sánchez JL, Zuluaga L, Uribe CS, Isaza R, Muñoz A, Arcos-Burgos M.
    Rev Neurol; 1967 Dec 23; 28(8):768-71. PubMed ID: 10363319
    [Abstract] [Full Text] [Related]

  • 49. Clinical, electroencephalographical and neuropharmacological studies in syndromes of progressive myoclonus epilepsy.
    Hambert O, Petersén I.
    Acta Neurol Scand; 1970 Dec 23; 46(2):149-86. PubMed ID: 4317270
    [No Abstract] [Full Text] [Related]

  • 50. [Juvenile myoclonic epilepsy].
    Simonsen N.
    Ugeskr Laeger; 1975 Oct 06; 137(41):2400-2. PubMed ID: 809883
    [No Abstract] [Full Text] [Related]

  • 51. [Myoclonic epilepsies in infancy].
    Palencia R.
    Rev Neurol; 2000 Jun 06; 30 Suppl 1():S15-24. PubMed ID: 10904965
    [Abstract] [Full Text] [Related]

  • 52. [The epileptic reaction of the central nervous system].
    Niedermeyer E.
    Hippokrates; 1967 Nov 30; 38(22):869-80. PubMed ID: 4968660
    [No Abstract] [Full Text] [Related]

  • 53. A study of the late form (type Lundborg) of progressive myoclonic epilepsy.
    Kraus-Ruppert R, Ostertag B, Häfner H.
    J Neurol Sci; 1970 Jul 30; 11(1):1-15. PubMed ID: 4194907
    [No Abstract] [Full Text] [Related]

  • 54. Lack of activation of human secondary somatosensory cortex in Unverricht-Lundborg type of progressive myoclonus epilepsy.
    Forss N, Silén T, Karjalainen T.
    Ann Neurol; 2001 Jan 30; 49(1):90-7. PubMed ID: 11198301
    [Abstract] [Full Text] [Related]

  • 55. Unverricht-Lundborg disease: absence of nonallelic genetic heterogeneity.
    Cochius JI, Figlewicz DA, Kälviäinen R, Nousiainen U, Farrell K, Patry G, Söderfeldt B, Frydman M, Lerman P, Andermann F.
    Ann Neurol; 1993 Nov 30; 34(5):739-41. PubMed ID: 8239570
    [Abstract] [Full Text] [Related]

  • 56. Dosing feasibility and tolerability of intranasal diazepam in adults with epilepsy.
    Sperling MR, Haas KF, Krauss G, Seif Eddeine H, Henney HR, Rabinowicz AL, Bream G, Squillacote D, Carrazana EJ.
    Epilepsia; 2014 Oct 30; 55(10):1544-50. PubMed ID: 25154625
    [Abstract] [Full Text] [Related]

  • 57. [Depakine in the treatment of essential or idiopathic epilepsy].
    Bergamini L, Mutani R, Furian PM, Riccio A.
    Schweiz Arch Neurol Neurochir Psychiatr; 1970 Jan 30; 106(1):1-7. PubMed ID: 4988895
    [No Abstract] [Full Text] [Related]

  • 58. Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.
    Lebas A, Guyant-Maréchal L, Hannequin D, Riant F, Tournier-Lasserve E, Parain D.
    Cephalalgia; 2008 Jul 30; 28(7):774-7. PubMed ID: 18498390
    [Abstract] [Full Text] [Related]

  • 59. [Primary generalized epilepsy in childhood. Clinico-statistical study].
    Borgheresi S, Luti E, Mecherini L, Buti Cossi D, Bardini MR.
    Minerva Pediatr; 1979 Nov 30; 31(22):1601-4. PubMed ID: 122150
    [No Abstract] [Full Text] [Related]

  • 60. [Therapeutic results of some benzodiazepines in chronic seizures in severe epilepsy in children].
    Miribel J, Marinier R.
    J Med Lyon; 1966 Nov 05; 47(108):1583-4 passim. PubMed ID: 4965896
    [No Abstract] [Full Text] [Related]

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