Yesim Parman
AuthID: R-00F-JNG
1
TITLE: Assessment of patients with hereditary transthyretin amyloidosis–understanding the impact of management and disease progression
AUTHORS: Conceição, I; Coelho, T; Rapezzi, C; Parman, Y; Obici, L; Galán, L; Rousseau, A;
PUBLISHED: 2019, SOURCE: Amyloid, VOLUME: 26, ISSUE: 3
AUTHORS: Conceição, I; Coelho, T; Rapezzi, C; Parman, Y; Obici, L; Galán, L; Rousseau, A;
PUBLISHED: 2019, SOURCE: Amyloid, VOLUME: 26, ISSUE: 3
INDEXED IN: Scopus
2
TITLE: Assessment of patients with hereditary transthyretin amyloidosis - understanding the impact of management and disease progression Full Text
AUTHORS: Isabel Conceicao; Teresa Coelho; Claudio Rapezzi; Yesim Parman; Laura Obici; Lucia Galan; Antoine Rousseau;
PUBLISHED: 2019, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 26, ISSUE: 3
AUTHORS: Isabel Conceicao; Teresa Coelho; Claudio Rapezzi; Yesim Parman; Laura Obici; Lucia Galan; Antoine Rousseau;
PUBLISHED: 2019, SOURCE: AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, VOLUME: 26, ISSUE: 3
INDEXED IN: WOS
3
TITLE: Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis
AUTHORS: 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; ...More
PUBLISHED: 2018, SOURCE: NEW ENGLAND JOURNAL OF MEDICINE, VOLUME: 379, ISSUE: 1
AUTHORS: 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; ...More
PUBLISHED: 2018, SOURCE: NEW ENGLAND JOURNAL OF MEDICINE, VOLUME: 379, ISSUE: 1
INDEXED IN: Scopus WOS
4
TITLE: 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
AUTHORS: Yesim Parman; David Adams; Laura Obici; Lucia Galan; Velina Guergueltcheva; Ole B Suhr; Teresa Coelho;
PUBLISHED: 2016, SOURCE: CURRENT OPINION IN NEUROLOGY, VOLUME: 29
AUTHORS: Yesim Parman; David Adams; Laura Obici; Lucia Galan; Velina Guergueltcheva; Ole B Suhr; Teresa Coelho;
PUBLISHED: 2016, SOURCE: CURRENT OPINION IN NEUROLOGY, VOLUME: 29
INDEXED IN: WOS
5
TITLE: Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia Full Text
AUTHORS: 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; ...More
PUBLISHED: 2012, SOURCE: NATURE GENETICS, VOLUME: 44, ISSUE: 10
AUTHORS: 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; ...More
PUBLISHED: 2012, SOURCE: NATURE GENETICS, VOLUME: 44, ISSUE: 10
INDEXED IN: Scopus WOS