BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

406 related articles for article (PubMed ID: 16302872)

  • 41. Idiopathic generalized epilepsies of adolescence.
    Beghi M; Beghi E; Cornaggia CM; Gobbi G
    Epilepsia; 2006; 47 Suppl 2():107-10. PubMed ID: 17105478
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Role of genetics in the diagnosis and treatment of epilepsy.
    Ferraro TN; Dlugos DJ; Buono RJ
    Expert Rev Neurother; 2006 Dec; 6(12):1789-800. PubMed ID: 17181426
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
    Zucca C; Redaelli F; Epifanio R; Zanotta N; Romeo A; Lodi M; Veggiotti P; Airoldi G; Panzeri C; Romaniello R; De Polo G; Bonanni P; Cardinali S; Baschirotto C; Martorell L; Borgatti R; Bresolin N; Bassi MT
    Arch Neurol; 2008 Apr; 65(4):489-94. PubMed ID: 18413471
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The epilepsies.
    Rees M; Gardiner RM
    Baillieres Clin Neurol; 1994 Aug; 3(2):297-313. PubMed ID: 7952849
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+).
    Scheffer IE; Harkin LA; Dibbens LM; Mulley JC; Berkovic SF
    Epilepsia; 2005; 46 Suppl 10():41-7. PubMed ID: 16359471
    [No Abstract]   [Full Text] [Related]  

  • 46. Idiopathic generalized epilepsies recognized by the International League Against Epilepsy.
    Nordli DR
    Epilepsia; 2005; 46 Suppl 9():48-56. PubMed ID: 16302875
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.
    Sander T; Hildmann T; Wienker TF; Ramel C; Beck-Mannagetta G; Bianchi A; Sailer U; Berek K; Bauer G; Neitzel H; Schmitz B; Durner M; Johnson KJ; Janz D
    Am J Med Genet; 1996 Feb; 67(1):31-9. PubMed ID: 8678111
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.
    Arsov T; Mullen SA; Rogers S; Phillips AM; Lawrence KM; Damiano JA; Goldberg-Stern H; Afawi Z; Kivity S; Trager C; Petrou S; Berkovic SF; Scheffer IE
    Ann Neurol; 2012 Nov; 72(5):807-15. PubMed ID: 23280796
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Gene defects in idiopathic epilepsy.
    Steinlein OK
    Rev Neurol (Paris); 1999 Jul; 155(6-7):450-3. PubMed ID: 10472657
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Clinical aspects of epileptic ion channel disorders].
    Campos-Castelló J; Canelón de López M; García-Fernández M
    Rev Neurol; 2000 Jun; 30 Suppl 1():S42-6. PubMed ID: 10904967
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Lack of an association between candidate gene loci and idiopathic generalized epilepsy in Kuwaiti Arab children.
    Haider MZ; Habeeb Y; Al-Nakkas E; Al-Anzi H; Zaki M; Al-Tawari A; Al-Bloushi M
    J Biomed Sci; 2005 Oct; 12(5):815-8. PubMed ID: 16205844
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy.
    Saint-Martin C; Gauvain G; Teodorescu G; Gourfinkel-An I; Fedirko E; Weber YG; Maljevic S; Ernst JP; Garcia-Olivares J; Fahlke C; Nabbout R; LeGuern E; Lerche H; Poncer JC; Depienne C
    Hum Mutat; 2009 Mar; 30(3):397-405. PubMed ID: 19191339
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15.
    Sander T; Kretz R; Williamson MP; Elmslie FV; Rees M; Hildmann T; Bianchi A; Bauer G; Sailer U; Scaramelli A; Schmitz B; Gardiner RM; Janz D; Beck-Mannagetta G
    Acta Neurol Scand; 1997 Jul; 96(1):1-7. PubMed ID: 9262125
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.
    Haug K; Kremerskothen J; Hallmann K; Sander T; Dullinger J; Rau B; Beyenburg S; Lentze MJ; Barnekow A; Elger CE; Propping P; Heils A
    Mol Cell Probes; 2000 Aug; 14(4):255-60. PubMed ID: 10970730
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
    Martínez-Juárez IE; Alonso ME; Medina MT; Durón RM; Bailey JN; López-Ruiz M; Ramos-Ramírez R; León L; Pineda G; Castroviejo IP; Silva R; Mija L; Perez-Gosiengfiao K; Machado-Salas J; Delgado-Escueta AV
    Brain; 2006 May; 129(Pt 5):1269-80. PubMed ID: 16520331
    [TBL] [Abstract][Full Text] [Related]  

  • 56. KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.
    Singh NA; Westenskow P; Charlier C; Pappas C; Leslie J; Dillon J; Anderson VE; Sanguinetti MC; Leppert MF;
    Brain; 2003 Dec; 126(Pt 12):2726-37. PubMed ID: 14534157
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations.
    Stogmann E; Lichtner P; Baumgartner C; Bonelli S; Assem-Hilger E; Leutmezer F; Schmied M; Hotzy C; Strom TM; Meitinger T; Zimprich F; Zimprich A
    Neurology; 2006 Dec; 67(11):2029-31. PubMed ID: 17159113
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Genetic Causes of Generalized Epilepsies.
    Helbig I
    Semin Neurol; 2015 Jun; 35(3):288-92. PubMed ID: 26060908
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Genetic abnormalities underlying familial epilepsy syndromes.
    Hirose S; Okada M; Yamakawa K; Sugawara T; Fukuma G; Ito M; Kaneko S; Mitsudome A
    Brain Dev; 2002 Jun; 24(4):211-22. PubMed ID: 12015163
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A case report of a family with overlapping features of autosomal dominant febrile seizures and GEFS+.
    Hindocha N; Nabbout R; Elmslie F; Makoff A; Al-Chalabi A; Nashef L
    Epilepsia; 2009 Apr; 50(4):937-42. PubMed ID: 19054398
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.