Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy.
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"Red-flag" symptom clusters in transthyretin familial amyloid polyneuropathyOcular Manifestations and Therapeutic Options in Patients with Familial Amyloid Polyneuropathy: A Systematic ReviewFirst European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathyRecommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosisSixty 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-FAPEvolving landscape in the management of transthyretin amyloidosisTransthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic AreaA woman with a rare p.Glu74Gly transthyretin mutation presenting exclusively with a rapidly progressive neuropathy: a case report.Rapid progression of familial amyloidotic polyneuropathy: a multinational natural history studyGenome-wide association analysis in dogs implicates 99 loci as risk variants for anterior cruciate ligament rupture.Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in FranceCurrent and future treatment of amyloid neuropathies.TTR kinetic stabilizers and TTR gene silencing: a new era in therapy for familial amyloidotic polyneuropathies.Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnoses.Elevation of plasma 1-deoxy-sphingolipids in type 2 diabetes mellitus: a susceptibility to neuropathy?Iatrogenic amyloid polyneuropathy after domino liver transplantation.Transthyretin familial amyloid polyneuropathy (TTR-FAP) in Mallorca: a comparison between late- and early-onset disease.A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK.Late-onset Familial Amyloidotic Polyneuropathy with Bence Jones Proteinuria and Cardiomyopathy.Phenotypic expressions of hereditary Transthyretin Ala97Ser related Amyloidosis (ATTR) in Taiwanese.Diagnostic challenges in hereditary transthyretin amyloidosis with polyneuropathy: avoiding misdiagnosis of a treatable hereditary neuropathyAssessing mNIS+7Ionis and international neurologists' proficiency in a familial amyloidotic polyneuropathy trial.Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm.Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
P2860
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P2860
Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Diagnostic hallmarks and pitfa ...... in-related amyloid-neuropathy.
@en
Diagnostic hallmarks and pitfa ...... in-related amyloid-neuropathy.
@nl
type
label
Diagnostic hallmarks and pitfa ...... in-related amyloid-neuropathy.
@en
Diagnostic hallmarks and pitfa ...... in-related amyloid-neuropathy.
@nl
prefLabel
Diagnostic hallmarks and pitfa ...... in-related amyloid-neuropathy.
@en
Diagnostic hallmarks and pitfa ...... in-related amyloid-neuropathy.
@nl
P2093
P2860
P50
P1433
P1476
Diagnostic hallmarks and pitfa ...... tin-related amyloid-neuropathy
@en
P2093
Andreas Ferbert
J Michael Schröder
Jean-Jacques Martin
Joachim Weis
Katrin Hinderhofer
Maike F Dohrn
Matthias Vorgerd
Peter Y Van den Bergh
P2860
P2888
P304
P356
10.1007/S00415-013-7124-7
P577
2013-10-08T00:00:00Z