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Author/Creator Bendahhou, Said

1. A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. (12th January 2016)

Authors:
Habbout, Karima; Poulin, Hugo; Rivier, François; Giuliano, Serena; Sternberg, Damien; Fontaine, Bertrand; Eymard, Bruno; Morales, Raul Juntas; Echenne, Bernard; King, Louise; Hanna, Michael G.; Männikkö, Roope; Chahine, Mohamed; Nicole, Sophie; Bendahhou, Said
Journal:
Neurology
Issue:
Volume 86:Number 2(2016)
Page Start:
Record Type:
Journal Article
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2. A204E mutation in Nav1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs. Issue 1 (December 2018)

Authors:
Kokunai, Yosuke; Dalle, Carine; Vicart, Savine; Sternberg, Damien; Pouliot, Valérie; Bendahhou, Said; Fournier, Emmanuel; Chahine, Mohamed; Fontaine, Bertrand; Nicole, Sophie
Journal:
Scientific reports
Issue:
Volume 8:Issue 1(2018)
Page Start:
1
Record Type:
Journal Article
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3. Phenotypical variability and atypical presentations in a French cohort of Andersen–Tawil syndrome. (4th May 2022)

Authors:
Villar‐Quiles, Rocio Nur; Sternberg, Damien; Tredez, Grégoire; Beatriz Romero, Norma; Evangelista, Teresinha; Lafôret, Pascal; Cintas, Pascal; Sole, Guilhem; Sacconi, Sabrina; Bendahhou, Said; Franques, Jérôme; Cances, Claude; Noury, JB; Delmont, Emilien; Blondy, Patricia; Perrin, Laurence; Hezod...
Journal:
European journal of neurology
Issue:
Volume 29:Number 8(2022)
Page Start:
2398
Record Type:
Journal Article
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