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-FAP (Q28078350)

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English	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-FAP	scientific article

Statements

scholarly article

1 reference

4 references

24 March 2019

22 April 2019

25 April 2019

1 October 2020

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-FAP (English)

1 reference

familial amyloid neuropathy

4 references

24 March 2019

22 April 2019

25 April 2019

1 October 2020

disease management

1 reference

1 October 2020

1

0 references

Velina Guergueltcheva

5

0 references

author name string

David Adams

2

1 reference

Laura Obici

3

1 reference

Lucía Galán

4

1 reference

Ole B. Suhr

6

1 reference

Teresa Coelho

7

1 reference

language of work or name

1 reference

publication date

February 2016

1 reference

1 February 2016

4 references

24 March 2019

22 April 2019

25 April 2019

1 October 2020

Current Opinion in Neurology

5 references

24 March 2019

22 April 2019

25 April 2019

1 October 2020

29 Suppl 1

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S3-S13

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copyright license

Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International

4 references

Europe PubMed Central

24 March 2019

Europe PubMed Central

22 April 2019

Europe PubMed Central

25 April 2019

Europe PubMed Central

1 October 2020

on focus list of Wikimedia project

0 references

Recommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

20 March 2017

First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

20 March 2017

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

1 reference

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20 March 2017

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

20 March 2017

Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Current and future treatment of amyloid neuropathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Epidemiology of transthyretin-associated familial amyloid polyneuropathy in the Majorcan area: Son Llàtzer Hospital descriptive study

1 reference

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29 September 2017

FAP neuropathy and emerging treatments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Familial amyloid polyneuropathy

1 reference

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29 September 2017

Recent advances in the treatment of familial amyloid polyneuropathy

1 reference

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29 September 2017

Guideline of transthyretin-related hereditary amyloidosis for clinicians.

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29 September 2017

Regional difference and similarity of familial amyloidosis with polyneuropathy in France

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Familial amyloid polyneuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

The molecular biology and clinical features of amyloid neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Genetic study of transthyretin amyloid neuropathies: carrier risks among French and Portuguese families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Hereditary and acquired amyloid neuropathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Transthyretin and familial amyloidotic polyneuropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Restless legs syndrome and nocturnal myoclonus: initial clinical manifestation of familial amyloid polyneuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Generalized amyloid in a family of Swedish origin. A study of 426 family members in seven generations of a new kinship with neuropathy, nephropathy, and central nervous system involvement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

29 September 2017

Familial amyloidotic polyneuropathy: current and emerging treatment options for transthyretin-mediated amyloidosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

2 June 2018

Familial amyloidotic polyneuropathy: description of an Italian kindred

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

2 June 2018

Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

2 June 2018

Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

2 June 2018

Most recent common ancestor ofTTRVal30Met mutation in Italian population and its potential role in genotype-phenotype correlation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

Frequency of the transthyretin Val30Met mutation in the northern Swedish population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

Overcoming artefact: anticipation in 284 Portuguese kindreds with familial amyloid polyneuropathy (FAP) ATTRV30M.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

The Transthyretin Amyloidosis Outcomes Survey (THAOS) registry: design and methodology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

Heart complications in familial transthyretin amyloidosis: impact of age and gender.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

Epidemiological, clinical and genetic study of familial amyloidotic polyneuropathy in Cyprus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

On the Origin of the Transthyretin Val30Met Familial Amyloid Polyneuropathy

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27 November 2018

Gender-related risk of myocardial involvement in systemic amyloidosis.

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27 November 2018

Myocardial hypertrophy and function are related to age at onset in familial amyloidotic polyneuropathy

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27 November 2018

Phenotypic and genotypic heterogeneity in transthyretin-related cardiac amyloidosis: towards tailoring of therapeutic strategies?

1 reference

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27 November 2018

Familial amyloidotic polyneuropathy with severe renal involvement in association with transthyretin Gly47Glu in Dutch, British and American-Finnish families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

Genetic epidemiology of familial amyloidotic polyneuropathy (FAP)-type I in Póvoa do Varzim and Vila do Conde (north of Portugal).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4739317

27 November 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The course and prognostic factors of familial amyloid polyneuropathy after liver transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[A prealbumin of human serum]

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyloid neuropathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of amyloid neuropathy in Europe

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic Area

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Familial type I (Portuguese form) amyloidotic polyneuropathy in Majorca. Study using the TTR (Met30) genetic marker]

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Length-dependent degeneration of fibers in Portuguese amyloid poly neuropathy: A clinicopathologic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family studies of the genetic abnormality in transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Liver transplantation for the treatment of type I familial amyloidotic polyneuropathy]

1 reference

https://pubmed.ncbi.nlm.nih.gov/26734951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1097/WCO.0000000000000288

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PubMed publication ID

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