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Andersen-Tawil Syndrome Presenting with Complete Heart Block.
Suetterlin K, Männikkö R, Flossmann E, Sud R, Fialho D, Vivekanandam V, James N, Gossios TD, Hanna MG, Savvatis K, Matthews E. Suetterlin K, et al. Among authors: fialho d. J Neuromuscul Dis. 2021;8(1):151-154. doi: 10.3233/JND-200572. J Neuromuscul Dis. 2021. PMID: 33074188
The primary periodic paralyses: diagnosis, pathogenesis and treatment.
Venance SL, Cannon SC, Fialho D, Fontaine B, Hanna MG, Ptacek LJ, Tristani-Firouzi M, Tawil R, Griggs RC; CINCH investigators. Venance SL, et al. Among authors: fialho d. Brain. 2006 Jan;129(Pt 1):8-17. doi: 10.1093/brain/awh639. Epub 2005 Sep 29. Brain. 2006. PMID: 16195244 Review.
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation.
Davies NP, Imbrici P, Fialho D, Herd C, Bilsland LG, Weber A, Mueller R, Hilton-Jones D, Ealing J, Boothman BR, Giunti P, Parsons LM, Thomas M, Manzur AY, Jurkat-Rott K, Lehmann-Horn F, Chinnery PF, Rose M, Kullmann DM, Hanna MG. Davies NP, et al. Among authors: fialho d. Neurology. 2005 Oct 11;65(7):1083-9. doi: 10.1212/01.wnl.0000178888.03767.74. Neurology. 2005. PMID: 16217063
Periodic paralysis.
Fialho D, Hanna MG. Fialho D, et al. Handb Clin Neurol. 2007;86:77-106. doi: 10.1016/S0072-9752(07)86004-0. Handb Clin Neurol. 2007. PMID: 18808996 No abstract available.
The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.
Matthews E, Fialho D, Tan SV, Venance SL, Cannon SC, Sternberg D, Fontaine B, Amato AA, Barohn RJ, Griggs RC, Hanna MG; CINCH Investigators. Matthews E, et al. Among authors: fialho d. Brain. 2010 Jan;133(Pt 1):9-22. doi: 10.1093/brain/awp294. Epub 2009 Nov 16. Brain. 2010. PMID: 19917643 Free PMC article. Review.
51 results