Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Helen J. Cross"'
Autor:
Joerg Klepper, Cigdem Akman, Marisa Armeno, Stéphane Auvin, Mackenzie Cervenka, Helen J. Cross, Valentina De Giorgis, Adela Della Marina, Kristin Engelstad, Nicole Heussinger, Eric H. Kossoff, Wilhelmina G. Leen, Baerbel Leiendecker, Umrao R. Monani, Hirokazu Oguni, Elizabeth Neal, Juan M. Pascual, Toni S. Pearson, Roser Pons, Ingrid E. Scheffer, Pierangelo Veggiotti, Michél Willemsen, Sameer M. Zuberi, Darryl C. De Vivo
Publikováno v:
Epilepsia Open, Vol 5, Iss 3, Pp 354-365 (2020)
Abstract Glut1 deficiency syndrome (Glut1DS) is a brain energy failure syndrome caused by impaired glucose transport across brain tissue barriers. Glucose diffusion across tissue barriers is facilitated by a family of proteins including glucose trans
Externí odkaz:
https://doaj.org/article/2fa0007690e94933a2416d2145d27364
Autor:
Nicola Specchio, Elaine C. Wirrell, Ingrid E. Scheffer, Rima Nabbout, Kate Riney, Pauline Samia, Marilisa Guerreiro, Sam Gwer, Sameer M. Zuberi, Jo M. Wilmshurst, Elissa Yozawitz, Ronit Pressler, Edouard Hirsch, Samuel Wiebe, Helen J. Cross, Emilio Perucca, Solomon L. Moshé, Paolo Tinuper, Stéphane Auvin
Publikováno v:
Epilepsia. 63:1398-1442
The 2017 International League Against Epilepsy classification has defined a three‐tier system with epilepsy syndrome identification at the third level. Although a syndrome cannot be determined in all children with epilepsy, identification of a spec
Publikováno v:
Epileptic disorders : international epilepsy journal with videotape. 22(S1)
Cannabis sativa L. is an ancient medicinal plant wherefrom over 120 cannabinoids are extracted. In the past two decades, there has been increasing interest in the therapeutic potential of cannabis-based treatments for neurological disorders such as e
Autor:
Alexis, Arzimanoglou, Helen J, Cross
Publikováno v:
Epileptic disorders : international epilepsy journal with videotape. 21(S1)
Encephalopathy related to Status Epilepticus during slow Sleep (ESES) is an age-dependent phenomenon, with usual spontaneous resolution during teenage years. However, cognitive outcome is often more disappointing, with permanent cognitive deficits in
Autor:
Carla, Marini, Davide, Mei, Teresa, Temudo, Anna Rita, Ferrari, Daniela, Buti, Charlotte, Dravet, Ana I, Dias, Ana, Moreira, Eulalia, Calado, Stefano, Seri, Brian, Neville, Juan, Narbona, Evan, Reid, Roberto, Michelucci, Federico, Sicca, Helen J, Cross, Renzo, Guerrini
Publikováno v:
Epilepsia. 48(9)
SCN1A is the most clinically relevant epilepsy gene, most mutations lead to severe myoclonic epilepsy of infancy (SMEI) and generalized epilepsy with febrile seizures plus (GEFS+). We studied 132 patients with epilepsy syndromes with seizures precipi