A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected (Q33673848)

28 July 2017

1 reference

title

A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected (English)

1 reference

28 July 2017

Coelho T

1

1 reference

28 July 2017

Sousa A

series ordinal

2

1 reference

28 July 2017

Lourenço E

series ordinal

3

1 reference

28 July 2017

Ramalheira J

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 April 1994

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

31

1 reference

28 July 2017

293-299

1 reference

28 July 2017

4

1 reference

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

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049801

Familial amyloidotic polyneuropathy in Sweden: a pedigree analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049801

Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049801

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049801

Familial amyloidotic polyneuropathy in Sweden: geographical distribution, age of onset, and prevalence

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049801

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049801

The genetic aspect of the familial amyloidotic polyneuropathy. Portuguese type of paramyloidosis

30 October 2018

1 reference

12 December 2020

Structurally abnormal transthyretin causing familial amyloidotic polyneuropathy in Sweden

1 reference

12 December 2020

Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis

1 reference

12 December 2020

Hereditary amyloidosis with polyneuropathy

1 reference

12 December 2020

Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial amyloidosis with polyneuropathy. A clinical study based on patients living in northern Sweden

1 reference

12 December 2020

Presence of an abnormal transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy

1 reference

12 December 2020

[PARAMYLOIDOSIS OF PERIPHERAL NERVES IN PORTUGAL]

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.31.4.293

1 reference

28 July 2017

1 reference

28 July 2017

1 reference