T-STAR gene: fine mapping in the candidate region for childhood absence epilepsy on 8q24 and mutational analysis in patients

By Sugimoto Y.   Morita R.   Amano K.   Shah P.U.   Pascual-Castroviejo I.   Khan S.   Delgado-Escueta A.V.   Yamakawa K.  

Epilepsy Research, Vol. 46, Iss. 2, 2001-08 ,pp. : 139-144

Elsevier

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Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME

By Moore T.   Hecquet S.   McLellann A.   Ville D.   Grid D.   Picard F.   Moulard B.   Asherson P.   Makoff A.J.   McCormick D.   Nashef L.   Froguel P.   Arzimanoglou A.   LeGuern E.   Bailleul B.  

Epilepsy Research, Vol. 46, Iss. 2, 2001-08 ,pp. : 157-167

Elsevier

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Linkage analysis between childhood absence epilepsy and genes encoding GABA A and GABA B receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q

By Robinson R.   Taske N.   Sander T.   Heils A.   Whitehouse W.   Goutieres F.   Aicardi J.   Lehesjoki A.-E.   Siren A.   Laue Friis M.   Kjeldsen M.J.   Panayiotopoulos C.   Kennedy C.   Ferrie C.   Rees M.   Gardiner R.M.  

Epilepsy Research, Vol. 48, Iss. 3, 2002-02 ,pp. : 169-179

Elsevier

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Long-term prognosis for childhood and juvenile absence epilepsy

By Trinka Eugen   Baumgartner Sarah   Unterberger Iris   Unterrainer Josef   Luef Gerhard   Haberlandt Edda   Bauer Gerhard  

Journal of Neurology, Vol. 251, Iss. 10, 2004-10 ,pp. : 1235-1241

Springer Publishing Company

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Childhood absence epilepsy and febrile seizures: a family with a GABA A receptor mutation

By Marini C.  

Brain, Vol. 126, Iss. 1, 2003-01 ,pp. : 230-240

Oxford University Press

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