Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24

By Morita R.   Miyazaki E.   Shah P.U.   Castroviejo I.P.   Delgado-Escueta A.V.   Yamakawa K.  

Epilepsy Research, Vol. 37, Iss. 2, 1999-11 ,pp. : 151-158

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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Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5

By Suzuki T.   Morita R.   Sugimoto Y.   Sugawara T.   Bai D.-S.   Alonso M.E.   Medina M.T.   Bailey J.N.   Rasmussen A.   Ramos-Peek J.   Cordova S.   Rubio-Donnadieu F.   Ochoa A.   Jara-Prado A.   Inazawa J.   Delgado-Escueta A.V.   Yamakawa K.  

Epilepsy Research, Vol. 50, Iss. 3, 2002-07 ,pp. : 265-275

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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