Genotype and Phenotype of Transthyretin Cardiac Amyloidosis in the United States: The Transthyretin Amyloid Outcome Survey (THAOS)

BACKGROUND: Transthyretin amyloidosis (ATTR) is a heterogeneous disorder with multiorgan involvement and a genetic or nongenetic basis. OBJECTIVES: We described ATTR in the United States in the THAOS (Transthyretin Amyloidosis Outcomes Survey) registry. METHODS: Demographic, clinical, and genetic fe...

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Bibliografiset tiedot
Julkaisussa:J Am Coll Cardiol
Päätekijät: Maurer, Mathew S., Hanna, Mazen, Grogan, Martha, Dispenzieri, Angela, Witteles, Ronald, Drachman, Brian, Judge, Daniel P., Lenihan, Daniel J., Gottlieb, Stephen S., Shah, Sanjiv J., Steidley, D. Eric, Ventura, Hector, Murali, Srinivas, Silver, Marc A., Jacoby, Daniel, Fedson, Savitri, Hummel, Scott L., Kristen, Arnt V., Damy, Thibaud, Planté-Bordeneuve, Violaine, Coelho, Teresa, Mundayat, Rajiv, Suhr, Ole B, Cruz, Márcia Waddington, Rapezzi, Claudio
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2016
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4940135/
https://ncbi.nlm.nih.gov/pubmed/27386769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacc.2016.03.596
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