Clinical characteristics and prognosis of Chinese patients with hereditary transthyretin amyloid cardiomyopathy
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Clinical characteristics and prognosis of Chinese patients with hereditary transthyretin amyloid cardiomyopathy
Authors
Keywords
-
Journal
Orphanet Journal of Rare Diseases
Volume 14, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2019-11-13
DOI
10.1186/s13023-019-1235-x
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Phenotypic profile of Ile68Leu transthyretin amyloidosis: an underdiagnosed cause of heart failure
- (2018) Christian Gagliardi et al. EUROPEAN JOURNAL OF HEART FAILURE
- Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy
- (2018) Mathew S. Maurer et al. NEW ENGLAND JOURNAL OF MEDICINE
- The identification of a transthyretin variant p.D38G in a Chinese family with early-onset leptomeningeal amyloidosis
- (2018) Kuan Fan et al. JOURNAL OF NEUROLOGY
- Familial amyloid polyneuropathy with chronic paroxysmal dry cough in Mainland China: A Chinese family with a proven heterozygous missense mutation c.349G>T in the transthyretin gene
- (2018) Zhenhua Yuan et al. JOURNAL OF CLINICAL NEUROSCIENCE
- Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths
- (2017) Esther González-López et al. EUROPEAN HEART JOURNAL
- Transthyretin V122I (pV142I)* cardiac amyloidosis: an age-dependent autosomal dominant cardiomyopathy too common to be overlooked as a cause of significant heart disease in elderly African Americans
- (2017) Joel N. Buxbaum et al. GENETICS IN MEDICINE
- Clinical features of familial amyloid polyneuropathy carrying transthyretin mutations in four Chinese kindreds
- (2017) Gonglu Liu et al. JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
- Aortic stenosis and transthyretin cardiac amyloidosis: the chicken or the egg?
- (2016) Arnault Galat et al. EUROPEAN HEART JOURNAL
- Genotype and Phenotype of Transthyretin Cardiac Amyloidosis
- (2016) Mathew S. Maurer et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Noninvasive Identification of ATTRwt Cardiac Amyloid: The Re-emergence of Nuclear Cardiology
- (2015) Mathew S. Maurer AMERICAN JOURNAL OF MEDICINE
- Hereditary ATTR amyloidosis: a single-institution experience with 266 patients
- (2015) Paul L. Swiecicki et al. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
- Hereditary Transthyretin Amyloidosis in Eight Chinese Families
- (2015) Yun Yuan et al. CHINESE MEDICAL JOURNAL
- Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction
- (2015) Esther González-López et al. EUROPEAN HEART JOURNAL
- A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK
- (2015) A S Carr et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Diagnosis, Prognosis, and Therapy of Transthyretin Amyloidosis
- (2015) Morie A. Gertz et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- The Amyloidogenic V122I Transthyretin Variant in Elderly Black Americans
- (2015) C. Cristina Quarta et al. NEW ENGLAND JOURNAL OF MEDICINE
- Transthyretin (TTR) Cardiac Amyloidosis
- (2012) Frederick L. Ruberg et al. CIRCULATION
- Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective
- (2012) C. Rapezzi et al. EUROPEAN HEART JOURNAL
- Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant
- (2011) P. T. Sattianayagam et al. EUROPEAN HEART JOURNAL
- TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?
- (2010) Bernard Bonaïti et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population
- (2008) Urban Hellman et al. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
- Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation inalpha2‐macroglobulinandtau: A population‐based autopsy study
- (2008) Maarit Tanskanen et al. ANNALS OF MEDICINE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now