These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 11968442)

  • 1. Genetics of idiopathic myoclonic epilepsies: an overview.
    Delgado-Escueta AV; Medina MT; Bai DS; Fong CY; Tanaka M; Alonso ME
    Adv Neurol; 2002; 89():161-84. PubMed ID: 11968442
    [No Abstract]   [Full Text] [Related]  

  • 2. Genetics of inherited epilepsies.
    Bate L; Gardiner M
    Epileptic Disord; 1999 Mar; 1(1):7-19. PubMed ID: 10937127
    [No Abstract]   [Full Text] [Related]  

  • 3. Segregation analysis of juvenile myoclonic epilepsy.
    Greenberg DA; Delgado-Escueta AV; Maldonado HM; Widelitz H
    Genet Epidemiol; 1988; 5(2):81-94. PubMed ID: 3136050
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Epilepsy and genetics].
    Poza JJ
    Neurologia; 2000; 15(7):278-87. PubMed ID: 11075576
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial benign nonprogressive myoclonic epilepsies.
    Striano P; de Falco FA; Minetti C; Zara F
    Epilepsia; 2009 May; 50 Suppl 5():37-40. PubMed ID: 19469844
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Eyelid myoclonia with absences (EMA)].
    Adachi M; Tsuneishi S; Nakamura H
    Ryoikibetsu Shokogun Shirizu; 2002; (37 Pt 6):341-5. PubMed ID: 12483897
    [No Abstract]   [Full Text] [Related]  

  • 7. Autosomal recessive benign myoclonic epilepsy of infancy.
    Zara F; De Falco FA
    Adv Neurol; 2005; 95():139-45. PubMed ID: 15508919
    [No Abstract]   [Full Text] [Related]  

  • 8. Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature.
    Haliloglu G; Chattopadhyay A; Skorodis L; Manzur A; Mercuri E; Talim B; Akçören Z; Renda Y; Muntoni F; Topaloğlu H
    Neuropediatrics; 2002 Dec; 33(6):314-9. PubMed ID: 12571787
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial adult myoclonic epilepsy (FAME).
    Uyama E; Fu YH; Ptácek LJ
    Adv Neurol; 2005; 95():281-8. PubMed ID: 15508931
    [No Abstract]   [Full Text] [Related]  

  • 10. [Clinical picture and type of myoclonus epilepsy with dominant heredity (author's transl)].
    Naito H; Kaji S
    Seishin Shinkeigaku Zasshi; 1979; 81(9):571-86. PubMed ID: 119245
    [No Abstract]   [Full Text] [Related]  

  • 11. Idiopathic epilepsies with a complex mode of inheritance.
    Serratosa JM
    Epilepsia; 1999; 40 Suppl 3():12-6. PubMed ID: 10446745
    [No Abstract]   [Full Text] [Related]  

  • 12. FAME 3: a novel form of progressive myoclonus and epilepsy.
    Carr JA; van der Walt PE; Nakayama J; Fu YH; Corfield V; Brink P; Ptacek L
    Neurology; 2007 Apr; 68(17):1382-9. PubMed ID: 17452583
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Severe myoclonic epilepsy in infancy: Dravet syndrome.
    Dravet C; Bureau M; Oguni H; Fukuyama Y; Cokar O
    Adv Neurol; 2005; 95():71-102. PubMed ID: 15508915
    [No Abstract]   [Full Text] [Related]  

  • 14. Myoclonic epilepsy and a maternally derived deletion of 15pter-->q13.
    Mizuguchi M; Tsukamoto K; Suzuki Y; Nakagome Y
    Clin Genet; 1994 Jan; 45(1):44-7. PubMed ID: 8149652
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort.
    Oguni H; Hayashi K; Osawa M; Awaya Y; Fukuyama Y; Fukuma G; Hirose S; Mitsudome A; Kaneko S
    Adv Neurol; 2005; 95():103-17. PubMed ID: 15508916
    [No Abstract]   [Full Text] [Related]  

  • 16. Autosomal dominant cortical myoclonus and epilepsy (ADCME) with linkage to chromosome 2p11.1-q12.2.
    Guerrini R; Parmeggiani L; Marini C; Brovedani P; Bonanni P
    Adv Neurol; 2005; 95():273-9. PubMed ID: 15508930
    [No Abstract]   [Full Text] [Related]  

  • 17. Is juvenile myoclonic epilepsy an autosomal recessive disease?
    Greenberg DA; Durner M; Delgado-Escueta AV; Janz D
    Ann Neurol; 1990 Jul; 28(1):110-1. PubMed ID: 2115759
    [No Abstract]   [Full Text] [Related]  

  • 18. SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures.
    Ebach K; Joos H; Doose H; Stephani U; Kurlemann G; Fiedler B; Hahn A; Hauser E; Hundt K; Holthausen H; Müller U; Neubauer BA
    Neuropediatrics; 2005 Jun; 36(3):210-3. PubMed ID: 15944908
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A case of Wolf-Hirschhorn syndrome progressing to resistant epilepsy.
    Unalp A; Uran N; Giray O; Ercal D
    Pediatr Neurol; 2007 Aug; 37(2):140-3. PubMed ID: 17675032
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation of a potassium channel-related gene in progressive myoclonic epilepsy.
    Van Bogaert P; Azizieh R; Désir J; Aeby A; De Meirleir L; Laes JF; Christiaens F; Abramowicz MJ
    Ann Neurol; 2007 Jun; 61(6):579-86. PubMed ID: 17455289
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.