Biochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis (Q30805928)

26 June 2017

title

Biochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis (English)

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26 June 2017

Shigeaki Mitsuhashi

1

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26 June 2017

Masahide Yazaki

2

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26 June 2017

Takahiko Tokuda

3

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26 June 2017

Yoshiki Sekijima

4

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26 June 2017

Yukihiko Washimi

5

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26 June 2017

Yuko Shimizu

6

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26 June 2017

Yukio Ando

7

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26 June 2017

Merrill D Benson

8

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26 June 2017

Shu-Ichi Ikeda

9

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26 June 2017

language of work or name

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1 December 2005

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26 June 2017

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26 June 2017

volume

12

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26 June 2017

issue

4

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26 June 2017

page(s)

216-225

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Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity.

26 June 2017

cites work

1 reference

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Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss).

21 January 2018

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Familial amyloid polyneuropathy associated with the transthyretin Cys114 gene in a Japanese kindred

21 January 2018

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Massive leptomeningeal amyloidosis associated with a Val30Met transthyretin gene

21 January 2018

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Transthyretin amyloidosis: a new mutation associated with dementia

21 January 2018

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Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis

21 January 2018

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Transthyretin amyloidosis and superficial siderosis of the CNS.

21 January 2018

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Oculoleptomeningeal amyloidosis associated with a new transthyretin variant Ser64.

21 January 2018

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https://api.crossref.org/works/10.1080/13506120500352404

Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His

21 January 2018

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Familial leptomeningeal amyloidosis with a transthyretin variant Asp18Gly representing repeated subarachnoid haemorrhages with superficial siderosis

21 January 2018

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D18G transthyretin is monomeric, aggregation prone, and not detectable in plasma and cerebrospinal fluid: a prescription for central nervous system amyloidosis?

21 January 2018

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Rapidly progressive amyloid polyneuropathy associated with a novel variant transthyretin serine 25.

21 January 2018

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Postmortem findings in two familial amyloidosis patients with transthyretin variant Asp38Ala

21 January 2018

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Novel variant transthyretin gene (Ser50 to Ile) in familial cardiac amyloidosis

21 January 2018

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Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis

21 January 2018

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Transthyretin Tyr69-to-Ile mutation (double-nucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome

21 January 2018

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Serum transthyretin monomer in patients with familial amyloid polyneuropathy

21 January 2018

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Paraneoplastic sensorimotor neuropathy and encephalopathy associated with anti-alpha-enolase antibody in a case of gastric adenocarcinoma

21 January 2018

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The biological and chemical basis for tissue-selective amyloid disease

21 January 2018

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Structure of prealbumin: secondary, tertiary and quaternary interactions determined by Fourier refinement at 1.8 A

21 January 2018

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Unusual Self-Association Properties of Transthyretin Y114C Related to Familial Amyloidotic Polyneuropathy: Effects on Detection and Quantification

21 January 2018

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The amyloidogenic potential of transthyretin variants correlates with their tendency to aggregate in solution

21 January 2018

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Tabulation of human transthyretin (TTR) variants, 2003

21 January 2018

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A Dutch kindred with familial amyloidotic polyneuropathy associated with the trans thy retin Cys 114 mutant

21 January 2018

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10.1080/13506120500352404

21 January 2018

Identifiers

DOI

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26 June 2017

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