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 *

78 related articles for article (PubMed ID: 9710024)

  • 21. No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.
    Sander T; Windemuth C; Schulz H; Saar K; Gennaro E; Bianchi A; Zara F; Bulteau C; Kaminska A; Ville D; Cieuta C; Prud'homme JF; Dulac O; Bate L; Gardiner RM; de Haan GJ; Janssen GA; Witte J; Halley DJ; Lindhout D; Wienker TF; Janz D;
    Am J Med Genet; 2002 Aug; 114(6):673-8. PubMed ID: 12210286
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Spastic paraplegia, epilepsy, and mental retardation in several members of a family: a novel genetic disorder.
    Gigli GL; Diomedi M; Bernardi G; Placidi F; Marciani MG; Calia E; Maschio MC; Neri G
    Am J Med Genet; 1993 Mar; 45(6):711-6. PubMed ID: 8456849
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
    ; Leu C; de Kovel CG; Zara F; Striano P; Pezzella M; Robbiano A; Bianchi A; Bisulli F; Coppola A; Giallonardo AT; Beccaria F; Trenité DK; Lindhout D; Gaus V; Schmitz B; Janz D; Weber YG; Becker F; Lerche H; Kleefuss-Lie AA; Hallman K; Kunz WS; Elger CE; Muhle H; Stephani U; Møller RS; Hjalgrim H; Mullen S; Scheffer IE; Berkovic SF; Everett KV; Gardiner MR; Marini C; Guerrini R; Lehesjoki AE; Siren A; Nabbout R; Baulac S; Leguern E; Serratosa JM; Rosenow F; Feucht M; Unterberger I; Covanis A; Suls A; Weckhuysen S; Kaneva R; Caglayan H; Turkdogan D; Baykan B; Bebek N; Ozbek U; Hempelmann A; Schulz H; Rüschendorf F; Trucks H; Nürnberg P; Avanzini G; Koeleman BP; Sander T
    Epilepsia; 2012 Feb; 53(2):308-18. PubMed ID: 22242659
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
    Hedera P; Blair MA; Andermann E; Andermann F; D'Agostino D; Taylor KA; Chahine L; Pandolfo M; Bradford Y; Haines JL; Abou-Khalil B
    Neurology; 2007 Jun; 68(24):2107-12. PubMed ID: 17377072
    [TBL] [Abstract][Full Text] [Related]  

  • 26. New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p.
    Nabbout R; Baulac S; Desguerre I; Bahi-Buisson N; Chiron C; Ruberg M; Dulac O; LeGuern E
    Neurology; 2007 Apr; 68(17):1374-81. PubMed ID: 17452582
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Linkage analysis of idiopathic generalised epilepsy in families of probands with Juvenile Myoclonic Epilepsy and marker loci in the region of EPM 1 on chromosome 21 q: Unverricht-Lundborg disease and JME are not allelic variants.
    Rees M; Curtis D; Parker K; Sundqvist A; Baralle D; Bespalova IN; Burmeister M; Chung E; Gardiner RM; Whitehouse WP
    Neuropediatrics; 1994 Feb; 25(1):20-5. PubMed ID: 8208346
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genome scan of idiopathic generalized epilepsy: evidence for major susceptibility gene and modifying genes influencing the seizure type.
    Durner M; Keddache MA; Tomasini L; Shinnar S; Resor SR; Cohen J; Harden C; Moshe SL; Rosenbaum D; Kang H; Ballaban-Gil K; Hertz S; Labar DR; Luciano D; Wallace S; Yohai D; Klotz I; Dicker E; Greenberg DA
    Ann Neurol; 2001 Mar; 49(3):328-35. PubMed ID: 11261507
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Paroxysmal kinesigenic dyskinesia and generalized seizures: clinical and genetic analysis in a Spanish pedigree.
    Cuenca-Leon E; Cormand B; Thomson T; Macaya A
    Neuropediatrics; 2002 Dec; 33(6):288-93. PubMed ID: 12571782
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients.
    Durner M; Sander T; Greenberg DA; Johnson K; Beck-Mannagetta G; Janz D
    Neurology; 1991 Oct; 41(10):1651-5. PubMed ID: 1922810
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Identification of a recombination event narrowing the Lafora disease gene region.
    Maddox LO; Descartes M; Collins J; Keating J; Rosenfeld S; Palmer C; Carroll AJ; Kuzniecky R
    J Med Genet; 1997 Jul; 34(7):590-1. PubMed ID: 9222970
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33.
    Dai XH; Chen WW; Wang X; Zhu QH; Li C; Li L; Liu MG; Wang QK; Liu JY
    Hum Genet; 2008 Nov; 124(4):423-9. PubMed ID: 18830713
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A gene causing autosomal recessive cataract maps to the short arm of chromosome 3.
    Pras E; Pras E; Bakhan T; Levy-Nissenbaum E; Lahat H; Assia EI; Garzozi HJ; Kastner DL; Goldman B; Frydman M
    Isr Med Assoc J; 2001 Aug; 3(8):559-62. PubMed ID: 11519376
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Preliminary localization of a gene for autosomal dominant hypoparathyroidism to chromosome 3q13.
    Finegold DN; Armitage MM; Galiani M; Matise TC; Pandian MR; Perry YM; Deka R; Ferrell RE
    Pediatr Res; 1994 Sep; 36(3):414-7. PubMed ID: 7808841
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Generalized paroxysmal fast activity in EEG: An unrecognized finding in genetic generalized epilepsy.
    Sagi V; Kim I; Bhatt AB; Sonmezturk H; Abou-Khalil BW; Arain AM
    Epilepsy Behav; 2017 Nov; 76():101-104. PubMed ID: 28874317
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Dominant partial epilepsies. A clinical, electrophysiological and genetic study of 19 European families.
    Picard F; Baulac S; Kahane P; Hirsch E; Sebastianelli R; Thomas P; Vigevano F; Genton P; Guerrini R; Gericke CA; An I; Rudolf G; Herman A; Brice A; Marescaux C; LeGuern E
    Brain; 2000 Jun; 123 ( Pt 6)():1247-62. PubMed ID: 10825362
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
    Charlier C; Singh NA; Ryan SG; Lewis TB; Reus BE; Leach RJ; Leppert M
    Nat Genet; 1998 Jan; 18(1):53-5. PubMed ID: 9425900
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29.
    Modamio-Høybjør S; Moreno-Pelayo MA; Mencía A; del Castillo I; Chardenoux S; Armenta D; Lathrop M; Petit C; Moreno F
    Hum Genet; 2003 Jan; 112(1):24-8. PubMed ID: 12483295
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A locus for autosomal dominant accessory auricular anomaly maps to 14q11.2-q12.
    Yang Y; Guo J; Liu Z; Tang S; Li N; Yang M; Pang Q; Fan F; Bu J; Yuan ST; Xiao X; Chen Y; Zhao K
    Hum Genet; 2006 Aug; 120(1):144-7. PubMed ID: 16775710
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22.
    Hedera P; Ma S; Blair MA; Taylor KA; Hamati A; Bradford Y; Abou-Khalil B; Haines JL
    Epilepsia; 2006 Oct; 47(10):1622-8. PubMed ID: 17054683
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.