Dravet Syndrome in Lebanon: First Report on Cases with <i>SCN1A</i> Mutations.

Alame, Saada; El-Houwayek, Eliane; Nava, Caroline; Sabbagh, Sandra; Fawaz, Ali; Gillart, Anne-Celine; Hasbini, Dana; Depienne, Christel; Mégarbané, André

Dravet Syndrome in Lebanon: First Report on Cases with SCN1A Mutations.

Alame, Saada; El-Houwayek, Eliane; Nava, Caroline; Sabbagh, Sandra; Fawaz, Ali; Gillart, Anne-Celine; Hasbini, Dana; Depienne, Christel; Mégarbané, André.

Afiliação

Alame S; Neuropediatrics Department, Lebanese University, Beirut, Lebanon.
El-Houwayek E; Pediatrics, Lebanese University, Beirut, Lebanon.
Nava C; Neuropediatrics, Hopital Universitaire des Enfants Reine Fabiola (HUDERF), Brussels, Belgium.
Sabbagh S; Inserm U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle épinière (ICM), F-75013 Paris, France.
Fawaz A; AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Département de Génétique, 75013 Paris, France.
Gillart AC; Service de Pediatrie, Hotel-Dieu de France, Beirut, Lebanon.
Hasbini D; Neuropediatrics Department, Lebanese University, Beirut, Lebanon.
Depienne C; Institut Jérôme Lejeune, Paris, France.
Mégarbané A; Neuropediatrics Department, Rafic Hariri University Hospital, Beirut, Lebanon.

Case Rep Med ; 2019: 5270503, 2019.

Article em En | MEDLINE | ID: mdl-30805006

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article