Characteristics of Patients with Late- vs. Early-Onset Val30Met Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey (THAOS)
出版年份 2021 全文链接
标题
Characteristics of Patients with Late- vs. Early-Onset Val30Met Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey (THAOS)
作者
关键词
-
出版物
Neurology and Therapy
Volume -, Issue -, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2021-05-23
DOI
10.1007/s40120-021-00258-z
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy
- (2020) David Adams et al. JOURNAL OF NEUROLOGY
- C1QA and C1QC modify age-at-onset in familial amyloid polyneuropathy patients
- (2019) Andreia Dias et al. Annals of Clinical and Translational Neurology
- Late-onset hereditary ATTR V30M amyloidosis with polyneuropathy: Characterization of Brazilian subjects from the THAOS registry
- (2019) MarcusVinicius Pinto et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Assessment of patients with hereditary transthyretin amyloidosis – understanding the impact of management and disease progression
- (2019) Isabel Conceição et al. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
- Transthyretin Amyloid Cardiomyopathy
- (2019) Frederick L. Ruberg et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- The morphology of amyloid fibrils and their impact on tissue damage in hereditary transthyretin amyloidosis: An ultrastructural study
- (2018) Haruki Koike et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Epidemiology of ATTRV30M neuropathy in Cyprus and the modifier effect of complement C1q on the age of disease onset
- (2018) Savanna Andreou et al. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
- Tafamidis delays neurological progression comparably across Val30Met and non-Val30Met genotypes in transthyretin familial amyloid polyneuropathy
- (2017) B. K. Gundapaneni et al. EUROPEAN JOURNAL OF NEUROLOGY
- One mutation, two distinct disease variants: unravelling the impact of transthyretin amyloid fibril composition
- (2017) O. B. Suhr et al. JOURNAL OF INTERNAL MEDICINE
- mtDNA copy number associated with age of onset in familial amyloid polyneuropathy
- (2017) Diana Santos et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy
- (2016) David Adams et al. CURRENT OPINION IN NEUROLOGY
- Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe
- (2016) Yesim Parman et al. CURRENT OPINION IN NEUROLOGY
- Clinical measures in transthyretin familial amyloid polyneuropathy
- (2016) Teresa Coelho et al. MUSCLE & NERVE
- Schwann cell and endothelial cell damage in transthyretin familial amyloid polyneuropathy
- (2016) Haruki Koike et al. NEUROLOGY
- Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M)
- (2015) Diana Santos et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Rapid progression of familial amyloidotic polyneuropathy
- (2015) David Adams et al. NEUROLOGY
- Amyloid Cardiomyopathy in Hereditary Transthyretin V30M Amyloidosis - Impact of Sex and Amyloid Fibril Composition
- (2015) Sandra Arvidsson et al. PLoS One
- Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis
- (2013) Elisabet Ihse et al. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
- Guideline of transthyretin-related hereditary amyloidosis for clinicians
- (2013) Yukio Ando et al. Orphanet Journal of Rare Diseases
- The Transthyretin Amyloidosis Outcomes Survey (THAOS) registry: design and methodology
- (2012) Violaine Planté-Bordeneuve et al. CURRENT MEDICAL RESEARCH AND OPINION
- Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas
- (2012) Haruki Koike et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Familial amyloid polyneuropathy
- (2011) Violaine Planté-Bordeneuve et al. LANCET NEUROLOGY
- Variation in amount of wild-type transthyretin in different fibril and tissue types in ATTR amyloidosis
- (2010) Elisabet Ihse et al. JOURNAL OF MOLECULAR MEDICINE-JMM
- Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients
- (2009) M Olsson et al. CLINICAL GENETICS
- Distinct characteristics of amyloid deposits in early- and late-onset transthyretin Val30Met familial amyloid polyneuropathy
- (2009) Haruki Koike et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
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