(Q26776343)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26663427%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

Laura Obici

3

1 reference

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9 June 2020

Hartmut H-J Schmidt

4

1 reference

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9 June 2020

author name string

Alejandra González-Duarte

2

1 reference

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9 June 2020

Damien Simoneau

5

1 reference

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9 June 2020

Moh-Lim Ong

6

1 reference

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9 June 2020

Leslie Amass

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26663427%20AND%20SRC:MED&resulttype=core&format=json

Journal of the Peripheral Nervous System

9 June 2020

language of work or name

English

0 references

publication date

March 2016

0 references

1 March 2016

3 references

24 March 2019

22 April 2019

25 April 2019

4 references

24 March 2019

22 April 2019

25 April 2019

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9 June 2020

volume

21

1 reference

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9 June 2020

page(s)

5-9

1 reference

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9 June 2020

issue

1

1 reference

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Creative Commons Attribution-NonCommercial-NoDerivatives

9 June 2020

copyright license

3 references

24 March 2019

22 April 2019

25 April 2019

on focus list of Wikimedia project

ScienceSource

0 references

cites work

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

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4788142

7 April 2017

Liver Transplantation for Hereditary Transthyretin Amyloidosis: After 20 Years Still the Best Therapeutic Alternative?

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4788142

A new prion disease: relationship with central and peripheral amyloidoses

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4788142

Transthyretin (ATTR) amyloidosis: clinical spectrum, molecular pathogenesis and disease-modifying treatments

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4788142

Update in the diagnosis and management of transthyretin familial amyloid polyneuropathy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4788142

FAP neuropathy and emerging treatments

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4788142

Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4788142

Guideline of transthyretin-related hereditary amyloidosis for clinicians.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4788142

Amyloid deposits in transthyretin-derived amyloidosis: cleaved transthyretin is associated with distinct amyloid morphology.

28 September 2017

1 reference

Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal.

21 January 2018

1 reference

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

21 January 2018

1 reference

Description of transthyretin S50A, S52P and G47A mutations in familial amyloidosis polyneuropathy

21 January 2018

1 reference

Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis.

21 January 2018

1 reference

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

21 January 2018

1 reference

Pathology of early- vs late-onset TTR Met30 familial amyloid polyneuropathy

21 January 2018

1 reference

Online registry for mutations in hereditary amyloidosis including nomenclature recommendations.

21 January 2018

1 reference

Macroglossia – not always AL amyloidosis

21 January 2018

1 reference

Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis

21 January 2018

1 reference

12 December 2020

Genotypic-phenotypic variations in a series of 65 patients with familial amyloid polyneuropathy

1 reference

12 December 2020

Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP)

1 reference

12 December 2020

Diagnosis of sporadic transthyretin Val30Met familial amyloid polyneuropathy: a practical analysis

1 reference

12 December 2020

Identifiers

DOI

10.1111/JNS.12153

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26663427%20AND%20SRC:MED&resulttype=core&format=json

release_fgwf377qw5aqbffcvhzrf42kqa

9 June 2020

Fatcat ID

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26663427%20AND%20SRC:MED&resulttype=core&format=json

9 June 2020

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26663427%20AND%20SRC:MED&resulttype=core&format=json