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Page 1
Phenotypical variability and atypical presentations in a French cohort of Andersen-Tawil syndrome.
Villar-Quiles RN, Sternberg D, Tredez G, Beatriz Romero N, Evangelista T, Lafôret P, Cintas P, Sole G, Sacconi S, Bendahhou S, Franques J, Cances C, Noury JB, Delmont E, Blondy P, Perrin L, Hezode M, Fournier E, Fontaine B, Stojkovic T, Vicart S. Villar-Quiles RN, et al. Among authors: bendahhou s. Eur J Neurol. 2022 Aug;29(8):2398-2411. doi: 10.1111/ene.15369. Epub 2022 May 4. Eur J Neurol. 2022. PMID: 35460302
A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.
Xia M, Jin Q, Bendahhou S, He Y, Larroque MM, Chen Y, Zhou Q, Yang Y, Liu Y, Liu B, Zhu Q, Zhou Y, Lin J, Liang B, Li L, Dong X, Pan Z, Wang R, Wan H, Qiu W, Xu W, Eurlings P, Barhanin J, Chen Y. Xia M, et al. Among authors: bendahhou s. Biochem Biophys Res Commun. 2005 Jul 15;332(4):1012-9. doi: 10.1016/j.bbrc.2005.05.054. Biochem Biophys Res Commun. 2005. PMID: 15922306
TWIK1, a unique background channel with variable ion selectivity.
Chatelain FC, Bichet D, Douguet D, Feliciangeli S, Bendahhou S, Reichold M, Warth R, Barhanin J, Lesage F. Chatelain FC, et al. Among authors: bendahhou s. Proc Natl Acad Sci U S A. 2012 Apr 3;109(14):5499-504. doi: 10.1073/pnas.1201132109. Epub 2012 Mar 19. Proc Natl Acad Sci U S A. 2012. PMID: 22431633 Free PMC article.
59 results