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: 9545186)

  • 1. Trisomy 12p and epilepsy with myoclonic absences.
    Elia M; Musumeci SA; Ferri R; Cammarata M
    Brain Dev; 1998 Mar; 20(2):127-30. PubMed ID: 9545186
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Myoclonic absence-like seizures and chromosome abnormality syndromes.
    Elia M; Guerrini R; Musumeci SA; Bonanni P; Gambardella A; Aguglia U
    Epilepsia; 1998 Jun; 39(6):660-3. PubMed ID: 9637609
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Perioral myoclonia with absences and myoclonic status aggravated by oxcarbazepine.
    Vrielynck P; Rostomashvili N; Degroote E; Ghariani S; van Rijckevorsel K
    Epileptic Disord; 2011 Sep; 13(3):308-12. PubMed ID: 21873142
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Eyelid myoclonia with absences in monozygotic twins.
    Adachi M; Inoue T; Tsuneishi S; Takada S; Nakamura H
    Pediatr Int; 2005 Jun; 47(3):343-7. PubMed ID: 15910466
    [No Abstract]   [Full Text] [Related]  

  • 5. A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study.
    Capovilla G; Rubboli G; Beccaria F; Lorenzetti ME; Montagnini A; Resi C; Gardella E; Gambardella A; Romeo A; Tassinari CA
    Epileptic Disord; 2001 Jun; 3(2):57-62. PubMed ID: 11431166
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Trisomy 12p syndrome: a chromosomal disorder associated with generalized 3-Hz spike and wave discharges.
    Guerrini R; Bureau M; Mattei MG; Battaglia A; Galland MC; Roger J
    Epilepsia; 1990; 31(5):557-66. PubMed ID: 2401247
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Absences in juvenile myoclonic epilepsy: a clinical and video-electroencephalographic study.
    Panayiotopoulos CP; Obeid T; Waheed G
    Ann Neurol; 1989 Apr; 25(4):391-7. PubMed ID: 2496640
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Juvenile myoclonic epilepsy in an elderly patient.
    Jacob S; Martin D; Rajabally YA
    Age Ageing; 2006 Mar; 35(2):194-6. PubMed ID: 16414965
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Idiopathic generalized epilepsy (IGE) syndromes in development: IGE with absences of early childhood, IGE with phantom absences, and perioral myoclonia with absences.
    Rubboli G; Gardella E; Capovilla G
    Epilepsia; 2009 May; 50 Suppl 5():24-8. PubMed ID: 19469842
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neck myoclonia with absence seizures in an Indian girl.
    Jain P; Sharma S; Aneja S
    J Child Neurol; 2014 Nov; 29(11):NP131-4. PubMed ID: 24556548
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Epilepsy and electroencephalographic findings in pericentric inversion of chromosome 12.
    Grosso S; Pucci L; Farnetani M; Di Bartolo RM; Galimberti D; Mostardini R; Anichini C; Balestri M; Morgese G; Balestri P
    J Child Neurol; 2004 Aug; 19(8):604-8. PubMed ID: 15605470
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epilepsy with myoclonic absences.
    Genton P; Bureau M
    CNS Drugs; 2006; 20(11):911-6. PubMed ID: 17044728
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Differentiation of typical absence seizures in epileptic syndromes. A video EEG study of 224 seizures in 20 patients.
    Panayiotopoulos CP; Obeid T; Waheed G
    Brain; 1989 Aug; 112 ( Pt 4)():1039-56. PubMed ID: 2505885
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Syndromic classification of patients with typical absence seizures.
    Guilhoto LM; Manreza ML; Yacubian EM
    Arq Neuropsiquiatr; 2003 Sep; 61(3A):580-7. PubMed ID: 14513161
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Myoclonic-astatic epilepsy.
    Doose H
    Epilepsy Res Suppl; 1992; 6():163-8. PubMed ID: 1418479
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Neck myoclonia with absence seizures: report of 3 cases.
    Yang Z; Liu X; Qin J; Jiang Y
    J Child Neurol; 2009 Aug; 24(8):1026-9. PubMed ID: 19666886
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Eyelid myoclonia with absences (EMA) in two monovular twins.
    DeMarco P
    Clin Electroencephalogr; 1989 Jul; 20(3):193-5. PubMed ID: 2502335
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Familial progressive myoclonus epilepsy (pme) (type Unverricht)].
    Herbstund A; Schröter P
    Psychiatr Neurol Med Psychol Beih; 1973; 17-18():100-17. PubMed ID: 4220172
    [No Abstract]   [Full Text] [Related]  

  • 20. Epilepsy with myoclonic absences.
    Bureau M; Tassinari CA
    Brain Dev; 2005 Apr; 27(3):178-84. PubMed ID: 15737698
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.