An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation.
about
Sixty 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-FAPFAP neuropathy and emerging treatments.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.Tongue atrophy and fasciculations in transthyretin familial amyloid neuropathy: An ALS mimicker.
P2860
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P2860
An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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name
An amyotrophic lateral scleros ...... novel transthyretin mutation.
@en
An amyotrophic lateral scleros ...... novel transthyretin mutation.
@nl
type
label
An amyotrophic lateral scleros ...... novel transthyretin mutation.
@en
An amyotrophic lateral scleros ...... novel transthyretin mutation.
@nl
prefLabel
An amyotrophic lateral scleros ...... novel transthyretin mutation.
@en
An amyotrophic lateral scleros ...... novel transthyretin mutation.
@nl
P2093
P2860
P1433
P1476
An amyotrophic lateral scleros ...... a novel transthyretin mutation
@en
P2093
Anne Richer
Catherine Lacroix
David Adams
Marie Theaudin
Michel Gugenheim
Micheline Misrahi
P2860
P304
P356
10.3109/13506129.2013.818535
P577
2013-08-05T00:00:00Z