(Q40807251)

23 September 2017

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title

Familial amyloid polyneuropathy (English)

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23 September 2017

Reilly MM

1

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23 September 2017

King RH

series ordinal

2

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23 September 2017

publication date

1 April 1993

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23 September 2017

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23 September 2017

volume

3

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23 September 2017

issue

2

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23 September 2017

page(s)

165-176

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A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves

23 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Familial amyloidotic polyneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Neuropathy, M components, and amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Variant apolipoprotein AI as a major constituent of a human hereditary amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Polyneuritic amyloidosis in a Japanese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Primary structure of an amyloid prealbumin and its plasma precursor in a heredofamilial polyneuropathy of Swedish origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Hereditary amyloid polyneuropathy in north west Ireland

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Irish (Donegal) amyloidosis is associated with the transthyretinALA60 (Appalachian) variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

A novel transthyretin mutation associated with familial amyloidotic polyneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

New mutant gene (transthyretin Arg 58) in cases with hereditary polyneuropathy detected by non-isotope method of single-strand conformation polymorphism analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Familial amyloidotic polyneuropathy presenting with carpal tunnel syndrome and a new transthyretin mutation, asparagine 70

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Inherited predisposition to generalized amyloidosis. Clinical and pathological study of a family with neuropathy, nephropathy, and peptic ulcer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Mutation in gelsolin gene in Finnish hereditary amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Peripheral nerve changes in amyloid neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Familial amyloid polyneuropathy: an electron microscope study of the peripheral nerve in five cases. I. Interstitial changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Familial amyloid polyneuropathy: an electron microscope study of the peripheral nerve in five cases. II. Nerve fibre changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Localization of the human prealbumin gene to chromosome 18.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

A new prealbumin variant in familial amyloid cardiomyopathy of Danish origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Fibril in senile systemic amyloidosis is derived from normal transthyretin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Recent advances in the molecular pathology of familial amyloid polyneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Production of recombinant human transthyretin with biological activities toward the understanding of the molecular basis of familial amyloidotic polyneuropathy (FAP).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Detection of single base changes in nucleic acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00741.X

10.1111/J.1750-3639.1993.TB00741.X

21 January 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference