Characterization of a familial case with primary erythromelalgia from Taiwan. (Q55043177)

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English	Characterization of a familial case with primary erythromelalgia from Taiwan.	scientific article

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instance of

scholarly article

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Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

title

Characterization of a familial case with primary erythromelalgia from Taiwan (English)

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stated in

Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

author

Chih-Chao Yang

series ordinal

6

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stated in

Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

Ming-Jen Lee

series ordinal

1

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Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

Sung-Tsang Hsieh

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3

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Europe PubMed Central

PubMed publication ID

17294067

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

author name string

Hsin-Su Yu

series ordinal

2

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Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

Dennis A Stephenson

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

Chien-Jung Lu

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

publication date

8 February 2007

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

published in

Journal of Neurology

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Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

volume

254

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Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

issue

2

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stated in

Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

page(s)

210-214

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Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

cites work

Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Erythromelalgia: vasculopathy, neuropathy, or both? A prospective study of vascular and neurophysiologic studies in erythromelalgia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lidocaine patch for pain of erythromelalgia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired neurogenic control of skin perfusion in erythromelalgia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lidocaine and mexiletine therapy for erythromelalgia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Erythromelalgia: a hereditary pain syndrome enters the molecular era.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autonomic Innervation of the Skin in Primary Erythermalgia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17294067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00415-006-0328-3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

Dimensions Publication ID

1014465511

0 references

PubMed publication ID

17294067

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17294067

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17294067%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 December 2019

 

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