Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Martine Eugie"'
Autor:
Ana Rita Salgueiro-Pereira, Fabrice Duprat, Paula A. Pousinha, Alexandre Loucif, Vincent Douchamps, Cristina Regondi, Marion Ayrault, Martine Eugie, Marion I. Stunault, Andrew Escayg, Romain Goutagny, Vadym Gnatkovsky, Carolina Frassoni, Hélène Marie, Ingrid Bethus, Massimo Mantegazza
Publikováno v:
Neurobiology of Disease, Vol 125, Iss , Pp 31-44 (2019)
SCN1A (NaV1.1 sodium channel) mutations cause Dravet syndrome (DS) and GEFS+ (which is in general milder), and are risk factors in other epilepsies. Phenotypic variability limits precision medicine in epilepsy, and it is important to identify factors
Externí odkaz:
https://doaj.org/article/8709f3f818c945c2a74432572ef04cdb
Autor:
Romain Goutagny, Hélène Marie, Ingrid Bethus, Martine Eugie, Andrew Escayg, Ana Rita Salgueiro-Pereira, Paula A. Pousinha, Marion I. Stunault, Vincent Douchamps, Alexandre J.C. Loucif, Vadym Gnatkovsky, Marion Ayrault, Fabrice Duprat, Massimo Mantegazza, Carolina Frassoni, Cristina Regondi
Publikováno v:
Neurobiology of Disease
Neurobiology of Disease, Elsevier, 2019, 125, pp.31-44. ⟨10.1016/j.nbd.2019.01.006⟩
Neurobiology of Disease, Vol 125, Iss, Pp 31-44 (2019)
Neurobiology of Disease, 2019, 125, pp.31-44. ⟨10.1016/j.nbd.2019.01.006⟩
Neurobiology of Disease, Elsevier, 2019, 125, pp.31-44. ⟨10.1016/j.nbd.2019.01.006⟩
Neurobiology of Disease, Vol 125, Iss, Pp 31-44 (2019)
Neurobiology of Disease, 2019, 125, pp.31-44. ⟨10.1016/j.nbd.2019.01.006⟩
International audience; SCN1A (NaV1.1 sodium channel) mutations cause Dravet syndrome (DS) and GEFS+ (which is in general milder), and are risk factors in other epilepsies. Phenotypic variability limits precision medicine in epilepsy, and it is impor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3146c1da3b3f4b3000af24b4e3fcb4c7
https://hal.archives-ouvertes.fr/hal-02166065
https://hal.archives-ouvertes.fr/hal-02166065
