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TÍTULO: Assessment of patients with hereditary transthyretin amyloidosis–understanding the impact of management and disease progression
AUTORES: Conceição, I; Coelho, T; Rapezzi, C; Parman, Y; Obici, L; Galán, L; Rousseau, A;
PUBLICAÇÃO: 2019, FONTE: Amyloid, VOLUME: 26, NÚMERO: 3
INDEXADO EM: Scopus
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TÍTULO: Assessment of patients with hereditary transthyretin amyloidosis - understanding the impact of management and disease progression  Full Text
AUTORES: Isabel Conceicao; Teresa Coelho; Claudio Rapezzi; Yesim Parman; Laura Obici; Lucia Galan; Antoine Rousseau;
PUBLICAÇÃO: 2019, FONTE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 26, NÚMERO: 3
INDEXADO EM: WOS
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TÍTULO: Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis
AUTORES: Adams, D; Gonzalez Duarte, A; O'Riordan, WD; Yang, CC; Ueda, M; Kristen, AV; Tournev, I; Schmidt, HH; Coelho, T; Berk, JL; Lin, KP; Vita, G; Attarian, S; Plante Bordeneuve, V; Mezei, MM; Campistol, JM; Buades, J; Brannagan, TH; Kim, BJ; Oh, J; Parman, Y; Sekijima, Y; Hawkins, PN; Solomon, SD; Polydefkis, M; Dyck, PJ; Gandhi, PJ; Goyal, S; Chen, J; Strahs, AL; Nochur, SV; Sweetser, MT; Garg, PP; Vaishnaw, AK; Gollob, JA; Suhr, OB; ...Mais
PUBLICAÇÃO: 2018, FONTE: NEW ENGLAND JOURNAL OF MEDICINE, VOLUME: 379, NÚMERO: 1
INDEXADO EM: Scopus WOS
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TÍTULO: Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns for TTR-FAP
AUTORES: Yesim Parman; David Adams; Laura Obici; Lucia Galan; Velina Guergueltcheva; Ole B Suhr; Teresa Coelho;
PUBLICAÇÃO: 2016, FONTE: CURRENT OPINION IN NEUROLOGY, VOLUME: 29
INDEXADO EM: WOS
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TÍTULO: Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia  Full Text
AUTORES: Magdalena Zimon; Jonathan Baets; Leonardo Almeida Souza; Els De Vriendt; Jelena Nikodinovic; Yesim Parman; Esra Battaloglu; Zeliha Matur; Velina Guergueltcheva; Ivailo Tournev; Michaela Auer Grumbach; Peter De Rijk; Britt Sabina Petersen; Thomas Mueller; Erik Fransen; Philip Van Damme; Wolfgang N Loescher; Nina Barisic; Zoran Mitrovic; Stefano C Previtali; Haluk Topaloglu; Guenther Bernert; Ana Beleza Meireles; Slobodanka Todorovic; Dusanka Savic Pavicevic; Boryana Ishpekova; Silvia Lechner; Kristien Peeters; Tinne Ooms; Angelika F Hahn; Stephan Zuechner; Vincent Timmerman; Patrick Van Dijck; Vedrana Milic Rasic; Andreas R Janecke; Peter De Jonghe; Albena Jordanova; ...Mais
PUBLICAÇÃO: 2012, FONTE: NATURE GENETICS, VOLUME: 44, NÚMERO: 10
INDEXADO EM: Scopus WOS