BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 18248446)

  • 1. An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder.
    Kugler SL; Bali B; Lieberman P; Strug L; Gagnon B; Murphy PL; Clarke T; Greenberg DA; Pal DK
    Epilepsia; 2008 Jun; 49(6):1086-90. PubMed ID: 18248446
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal dominant rolandic epilepsy with speech dyspraxia.
    Scheffer IE
    Epileptic Disord; 2000; 2 Suppl 1():S19-22. PubMed ID: 11231219
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant inheritance of centrotemporal sharp waves in rolandic epilepsy families.
    Bali B; Kull LL; Strug LJ; Clarke T; Murphy PL; Akman CI; Greenberg DA; Pal DK
    Epilepsia; 2007 Dec; 48(12):2266-72. PubMed ID: 17662063
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions.
    Neubauer BA; Moises HW; Lässker U; Waltz S; Diebold U; Stephani U
    Epilepsia; 1997 Jul; 38(7):782-7. PubMed ID: 9579905
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.
    Neubauer BA; Fiedler B; Himmelein B; Kämpfer F; Lässker U; Schwabe G; Spanier I; Tams D; Bretscher C; Moldenhauer K; Kurlemann G; Weise S; Tedroff K; Eeg-Olofsson O; Wadelius C; Stephani U
    Neurology; 1998 Dec; 51(6):1608-12. PubMed ID: 9855510
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pleiotropic effects of the 11p13 locus on developmental verbal dyspraxia and EEG centrotemporal sharp waves.
    Pal DK; Li W; Clarke T; Lieberman P; Strug LJ
    Genes Brain Behav; 2010 Nov; 9(8):1004-12. PubMed ID: 20825490
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autosomal dominant rolandic epilepsy and speech dyspraxia: a new syndrome with anticipation.
    Scheffer IE; Jones L; Pozzebon M; Howell RA; Saling MM; Berkovic SF
    Ann Neurol; 1995 Oct; 38(4):633-42. PubMed ID: 7574460
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).
    Strug LJ; Clarke T; Chiang T; Chien M; Baskurt Z; Li W; Dorfman R; Bali B; Wirrell E; Kugler SL; Mandelbaum DE; Wolf SM; McGoldrick P; Hardison H; Novotny EJ; Ju J; Greenberg DA; Russo JJ; Pal DK
    Eur J Hum Genet; 2009 Sep; 17(9):1171-81. PubMed ID: 19172991
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The genetics of rolandic epilepsy.
    Neubauer BA
    Epileptic Disord; 2000; 2 Suppl 1():S67-8. PubMed ID: 11231229
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Idiopathic partial epilepsy: electroclinical demonstration of a prolonged seizure with sequential rolandic and occipital involvement. Seizure spread due to regional susceptibility?
    Parmeggiani L; Guerrini R
    Epileptic Disord; 1999 Mar; 1(1):35-40. PubMed ID: 10937130
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.
    Guerrini R; Bonanni P; Nardocci N; Parmeggiani L; Piccirilli M; De Fusco M; Aridon P; Ballabio A; Carrozzo R; Casari G
    Ann Neurol; 1999 Mar; 45(3):344-52. PubMed ID: 10072049
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Typical benign epilepsy potentials in childhood (Rolandic spikes)--neurobiological and neuropsychological symptoms and their clinical significance in child and adolescent psychiatry].
    Holtmann M; Becker K; el-Faddagh M; Schmidt MH
    Z Kinder Jugendpsychiatr Psychother; 2004 May; 32(2):117-29. PubMed ID: 15181787
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autistic regression with rolandic spikes.
    Nass R; Devinsky O
    Neuropsychiatry Neuropsychol Behav Neurol; 1999 Jul; 12(3):193-7. PubMed ID: 10456804
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
    Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Bifocal atypical rolandic epilepsy with speech dyspraxia].
    Karlov VA; Baiarrnaa Dondovyn ; Gnezditskiĭ VV
    Zh Nevrol Psikhiatr Im S S Korsakova; 2004; 104(12):4-9. PubMed ID: 15849864
    [TBL] [Abstract][Full Text] [Related]  

  • 16. EEG criteria predictive of complicated evolution in idiopathic rolandic epilepsy.
    Massa R; de Saint-Martin A; Carcangiu R; Rudolf G; Seegmuller C; Kleitz C; Metz-Lutz MN; Hirsch E; Marescaux C
    Neurology; 2001 Sep; 57(6):1071-9. PubMed ID: 11571336
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci.
    Addis L; Chiang T; Clarke T; Hardison H; Kugler S; Mandelbaum DE; Novotny E; Wolf S; Strug LJ; Pal DK
    Genes Brain Behav; 2014 Mar; 13(3):333-40. PubMed ID: 24286483
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exclusion of linkage of genetic focal sharp waves to the HLA region on chromosome 6p in families with benign partial epilepsy with centrotemporal sharp waves.
    Whitehouse W; Diebold U; Rees M; Parker K; Doose H; Gardiner RM
    Neuropediatrics; 1993 Aug; 24(4):208-10. PubMed ID: 8232778
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Benign rolandic epilepsy investigated by magnetoencephalography.
    Kamada K; Möller M; Saguer M; Kassubek J; Kober H; Wenzel D; Vieth JB
    Biomed Tech (Berl); 1997; 42 Suppl():185-7. PubMed ID: 9517106
    [No Abstract]   [Full Text] [Related]  

  • 20. [The atypical developments of rolandic epilepsy are predictable complications].
    Pesántez-Ríos G; Martínez-Bermejo A; Arcas J; Merino-Andreu M; Ugalde-Canitrot A
    Rev Neurol; 2015 Aug; 61(3):106-13. PubMed ID: 26178515
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.