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FAP neuropathy and emerging treatments.
Adams D, Théaudin M, Cauquil C, Algalarrondo V, Slama M. Adams D, et al. Among authors: slama m. Curr Neurol Neurosci Rep. 2014 Mar;14(3):435. doi: 10.1007/s11910-013-0435-3. Curr Neurol Neurosci Rep. 2014. PMID: 24482069 Review.
Prevalence and clinical phenotype of hereditary transthyretin amyloid cardiomyopathy in patients with increased left ventricular wall thickness.
Damy T, Costes B, Hagège AA, Donal E, Eicher JC, Slama M, Guellich A, Rappeneau S, Gueffet JP, Logeart D, Planté-Bordeneuve V, Bouvaist H, Huttin O, Mulak G, Dubois-Randé JL, Goossens M, Canoui-Poitrine F, Buxbaum JN. Damy T, et al. Among authors: slama m. Eur Heart J. 2016 Jun 14;37(23):1826-34. doi: 10.1093/eurheartj/ehv583. Epub 2015 Nov 3. Eur Heart J. 2016. PMID: 26537620 Clinical Trial.
[Treatment of familial amyloid polyneuropathy].
Adams D, Samuel D, Slama M. Adams D, et al. Among authors: slama m. Presse Med. 2012 Sep;41(9 Pt 1):793-806. doi: 10.1016/j.lpm.2011.11.027. Epub 2012 Feb 16. Presse Med. 2012. PMID: 22341949 French.
Aortic stenosis and transthyretin cardiac amyloidosis: the chicken or the egg?
Galat A, Guellich A, Bodez D, Slama M, Dijos M, Zeitoun DM, Milleron O, Attias D, Dubois-Randé JL, Mohty D, Audureau E, Teiger E, Rosso J, Monin JL, Damy T. Galat A, et al. Among authors: slama m. Eur Heart J. 2016 Dec 14;37(47):3525-3531. doi: 10.1093/eurheartj/ehw033. Epub 2016 Feb 22. Eur Heart J. 2016. PMID: 26908951
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