Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser.
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Neuromuscular abnormality and autonomic dysfunction in patients with cerebrotendinous xanthomatosis.FAP neuropathy and emerging treatments.The Temporal Profiles of Changes in Nerve Excitability Indices in Familial Amyloid Polyneuropathy.Effect of glycemic control on sudomotor denervation in type 2 diabetes.Structural and functional characterization of nerve fibres in polyneuropathy and healthy subjects.Amyloid neuropathies.Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in FranceSudomotor innervation in transthyretin amyloid neuropathy: Pathology and functional correlates.Current and future treatment of amyloid neuropathies.Hypothalamic gene expression profile indicates a reduction in G protein signaling in the Wfs1 mutant mice.Progress in the treatment of small fiber peripheral neuropathy.TTR kinetic stabilizers and TTR gene silencing: a new era in therapy for familial amyloidotic polyneuropathies.Cutaneous nerve biomarkers in transthyretin familial amyloid polyneuropathy.A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK.Transthyretin amyloid neuropathy has earlier neural involvement but better prognosis than primary amyloid counterpart: an answer to the paradox?Phenotypic expressions of hereditary Transthyretin Ala97Ser related Amyloidosis (ATTR) in Taiwanese.Familial amyloidotic polyneuropathy: current and emerging treatment options for transthyretin-mediated amyloidosis.Tyr78Phe Transthyretin Mutation with Predominant Motor Neuropathy as the Initial Presentation.A prospective, observational study of patients with uncommon distal symmetric painful small-fiber neuropathy.Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients.Effect on disability and safety of Tafamidis in late onset of Met30 transthyretin familial amyloid polyneuropathy.Clinical features of familial amyloid polyneuropathy carrying transthyretin mutations in four Chinese kindreds.A Missense Variant p.Ala117Ser in the Transthyretin Gene of a Han Chinese Family with Familial Amyloid Polyneuropathy.Familial amyloidotic polineuropathy and systemic lupus.
P2860
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P2860
Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Clinical presentations and ski ...... due to transthyretin Ala97Ser.
@en
Clinical presentations and ski ...... due to transthyretin Ala97Ser.
@nl
type
label
Clinical presentations and ski ...... due to transthyretin Ala97Ser.
@en
Clinical presentations and ski ...... due to transthyretin Ala97Ser.
@nl
prefLabel
Clinical presentations and ski ...... due to transthyretin Ala97Ser.
@en
Clinical presentations and ski ...... due to transthyretin Ala97Ser.
@nl
P2093
P50
P1433
P1476
Clinical presentations and ski ...... due to transthyretin Ala97Ser
@en
P2093
N C-C Yang
Y-T Chuang
P304
P356
10.1212/WNL.0B013E3181EC7FDA
P407
P577
2010-08-01T00:00:00Z