Description of a large cohort of Caucasian patients with V122I ATTRv amyloidosis: Neurological and cardiological features
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Title
Description of a large cohort of Caucasian patients with
V122I ATTRv
amyloidosis: Neurological and cardiological features
Authors
Keywords
-
Journal
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2020-05-12
DOI
10.1111/jns.12385
References
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Related references
Note: Only part of the references are listed.- Increased Risk of Multiple Outpatient Surgeries in African-American Carriers of Transthyretin Val122Ile Mutation Is Modulated by Non-Coding Variants
- (2019) Renato Polimanti et al. Journal of Clinical Medicine
- Association between hearing loss and hereditary ATTR amyloidosis
- (2019) Sophie Bartier et al. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
- Phenome-wide association study of TTR and RBP4 genes in 361,194 individuals reveals novel insights in the genetics of hereditary and wildtype transthyretin amyloidoses
- (2019) Antonella De Lillo et al. HUMAN GENETICS
- Sporadic Cardiac Amyloidosis by Amyloidogenic Transthyretin V122I Variant
- (2019) Takeshi Nehashi et al. International Heart Journal
- Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry
- (2019) Scott M. Damrauer et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Monoclonal gammopathy of undetermined significance in systemic transthyretin amyloidosis (ATTR)
- (2018) Pooja Phull et al. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
- Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy
- (2018) Mathew S. Maurer et al. NEW ENGLAND JOURNAL OF MEDICINE
- 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
- Val122Ile mt-ATTR Has a Worse Survival Than wt-ATTR Cardiac Amyloidosis
- (2017) Avinainder Singh et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- The Val142Ile transthyretin cardiac amyloidosis
- (2016) Francesco Cappelli et al. Journal of Cardiovascular Medicine
- Genotype and Phenotype of Transthyretin Cardiac Amyloidosis
- (2016) Mathew S. Maurer et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Phenotypic variability of TTR Val122Ile mutation: a Caucasian patient with axonal neuropathy and normal heart
- (2016) Claudia Stancanelli et al. NEUROLOGICAL SCIENCES
- Hereditary ATTR amyloidosis: a single-institution experience with 266 patients
- (2015) Paul L. Swiecicki et al. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
- The Amyloidogenic V122I Transthyretin Variant in Elderly Black Americans
- (2015) C. Cristina Quarta et al. NEW ENGLAND JOURNAL OF MEDICINE
- Homozygosity for the V122I Mutation in Transthyretin Is Associated with Earlier Onset of Cardiac Amyloidosis in the African American Population in the Seventh Decade of Life
- (2013) Honey V. Reddi et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Guideline of transthyretin-related hereditary amyloidosis for clinicians
- (2013) Yukio Ando et al. Orphanet Journal of Rare Diseases
- Transthyretin-related familial amyloidotic polyneuropathy: description of a cohort of patients with Leu64 mutation and late onset
- (2012) Massimo Russo et al. JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
- Familial amyloid polyneuropathy
- (2011) Violaine Planté-Bordeneuve et al. LANCET NEUROLOGY
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