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 *

145 related articles for article (PubMed ID: 15048902)

  • 1. Genetic variation of CACNA1H in idiopathic generalized epilepsy.
    Heron SE; Phillips HA; Mulley JC; Mazarib A; Neufeld MY; Berkovic SF; Scheffer IE
    Ann Neurol; 2004 Apr; 55(4):595-6. PubMed ID: 15048902
    [No Abstract]   [Full Text] [Related]  

  • 2. Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.
    Heron SE; Khosravani H; Varela D; Bladen C; Williams TC; Newman MR; Scheffer IE; Berkovic SF; Mulley JC; Zamponi GW
    Ann Neurol; 2007 Dec; 62(6):560-8. PubMed ID: 17696120
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Effects of Cav3.2 channel mutations linked to idiopathic generalized epilepsy.
    Khosravani H; Bladen C; Parker DB; Snutch TP; McRory JE; Zamponi GW
    Ann Neurol; 2005 May; 57(5):745-9. PubMed ID: 15852375
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A profile of alternative RNA splicing and transcript variation of CACNA1H, a human T-channel gene candidate for idiopathic generalized epilepsies.
    Zhong X; Liu JR; Kyle JW; Hanck DA; Agnew WS
    Hum Mol Genet; 2006 May; 15(9):1497-512. PubMed ID: 16565161
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association between genetic variation of CACNA1H and childhood absence epilepsy.
    Chen Y; Lu J; Pan H; Zhang Y; Wu H; Xu K; Liu X; Jiang Y; Bao X; Yao Z; Ding K; Lo WH; Qiang B; Chan P; Shen Y; Wu X
    Ann Neurol; 2003 Aug; 54(2):239-43. PubMed ID: 12891677
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene.
    Kapoor A; Satishchandra P; Ratnapriya R; Reddy R; Kadandale J; Shankar SK; Anand A
    Ann Neurol; 2008 Aug; 64(2):158-67. PubMed ID: 18756473
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and genetic study of Tunisian families with genetic generalized epilepsy: contribution of CACNA1H and MAST4 genes.
    Landoulsi Z; Laatar F; NoƩ E; Mrabet S; Ben Djebara M; Achaz G; Nava C; Baulac S; Kacem I; Gargouri-Berrechid A; Gouider R; Leguern E
    Neurogenetics; 2018 Aug; 19(3):165-178. PubMed ID: 29948376
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association between D18S474 locus on chromosome 18q12 and idiopathic generalized epilepsy.
    Lucarelli P; Rizzo R; Gagliano A; Palmarino M; Volzone A; Arpino C; Curatolo P
    Brain Dev; 2007 Jan; 29(1):9-12. PubMed ID: 16790332
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Copy number variants--an unexpected risk factor for the idiopathic generalized epilepsies.
    Scheffer IE; Berkovic SF
    Brain; 2010 Jan; 133(Pt 1):7-8. PubMed ID: 20047903
    [No Abstract]   [Full Text] [Related]  

  • 11. Pathogenic Cav3.2 channel mutation in a child with primary generalized epilepsy.
    Souza IA; Gandini MA; Zhang FX; Mitchell WG; Matsumoto J; Lerner J; Pierson TM; Zamponi GW
    Mol Brain; 2019 Oct; 12(1):86. PubMed ID: 31651342
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epilepsy genetics: yet more exciting news.
    Lowenstein D; Messing R
    Ann Neurol; 2007 Dec; 62(6):549-50. PubMed ID: 17932953
    [No Abstract]   [Full Text] [Related]  

  • 13. Susceptibility genes for complex epilepsy.
    Mulley JC; Scheffer IE; Harkin LA; Berkovic SF; Dibbens LM
    Hum Mol Genet; 2005 Oct; 14 Spec No. 2():R243-9. PubMed ID: 16244322
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.
    Marini C; Scheffer IE; Crossland KM; Grinton BE; Phillips FL; McMahon JM; Turner SJ; Dean JT; Kivity S; Mazarib A; Neufeld MY; Korczyn AD; Harkin LA; Dibbens LM; Wallace RH; Mulley JC; Berkovic SF
    Epilepsia; 2004 May; 45(5):467-78. PubMed ID: 15101828
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Biparental inheritance in idiopathic generalized epilepsy.
    Jansen AC; Andermann E; Andermann F
    Epilepsia; 2004 Oct; 45(10):1294-5. PubMed ID: 15461686
    [No Abstract]   [Full Text] [Related]  

  • 16. Genetics of idiopathic generalized epilepsies.
    Gardiner M
    Epilepsia; 2005; 46 Suppl 9():15-20. PubMed ID: 16302872
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular characterization of T-type calcium channels.
    Perez-Reyes E
    Cell Calcium; 2006 Aug; 40(2):89-96. PubMed ID: 16759699
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The effect of CACNA1H gene G773D mutation on calcium channel function].
    Wang JL; Han CY; Jing YH; Chen YC; Feng N; Lu JJ; Zhang YH; Pan H; Wu HS; Xu KM; Jiang YW; Liang JM; Wang L; Wang XL; Shen Y; Wu XR
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):369-73. PubMed ID: 16883519
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SCN1A variant in a Scandinavian GEFS+ family: a wolf in sheep's clothing?
    Holland KD
    Acta Neurol Scand; 2008 Nov; 118(5):344-5; author reply 346. PubMed ID: 18616623
    [No Abstract]   [Full Text] [Related]  

  • 20. Familial generalized epilepsy in Bulgarian Roma.
    Tournev I; Royer B; Szepetowski P; Guergueltcheva V; Radionova M; Velizarova R; Yonova M; Lathrop M; Jamali S; Petkov R; Raycheva M; Genton P
    Epileptic Disord; 2007 Sep; 9(3):300-6. PubMed ID: 17884754
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.