Molecular genetics of amyloid neuropathy in Europe (Q69367916)

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1 October 2019

title

Molecular genetics of amyloid neuropathy in Europe (English)

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1 October 2019

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1

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1 October 2019

author name string

A E Harding

2

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1 October 2019

L Middleton

3

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1 October 2019

G Chrysostomou

4

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1 October 2019

G Said

5

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1 October 2019

R H King

6

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1 October 2019

P K Thomas

7

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1 October 2019

language of work or name

English

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publication date

1 March 1989

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1 October 2019

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1 October 2019

volume

1

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1 October 2019

issue

8637

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1 October 2019

page(s)

524-526

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

1 October 2019

cites work

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7 January 2021

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy

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7 January 2021

Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).

1 reference

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7 January 2021

Identification of carriers of mutant prealbumin gene associated with familial amyloidotic polyneuropathy type I by Southern blot procedures: study of six pedigrees in the Arao district of Japan

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy

1 reference

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7 January 2021

Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis

1 reference

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7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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7 January 2021

Polyneuritic amyloidosis in a Japanese family

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7 January 2021

Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)

1 reference

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7 January 2021

Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family

1 reference

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7 January 2021

Onset in the seventh decade and lack of symptoms in heterozygotes for the TTRMet30 mutation in hereditary amyloid neuropathy—type I (Portuguese, Andrade)

1 reference

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7 January 2021

10.1016/S0140-6736(89)90068-8

Identifiers

DOI

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1 October 2019

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