(Q38030606)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22845492%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

title

Human Mendelian pain disorders: a key to discovery and validation of novel analgesics (English)

1 reference

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9 February 2020

7

1 reference

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9 February 2020

author name string

Y P Goldberg

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22845492%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

S N Pimstone

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22845492%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

R Namdari

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22845492%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

N Price

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22845492%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

C Cohen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22845492%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

R P Sherrington

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22845492%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

publication date

13 August 2012

1 reference

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9 February 2020

1 reference

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9 February 2020

volume

82

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22845492%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

issue

4

1 reference

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9 February 2020

page(s)

367-373

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22845492%20AND%20SRC:MED&resulttype=core&format=json

The lateralisation of pain

9 February 2020

cites work

1 reference

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A difficult balance--pain management, drug safety, and the FDA.

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The productivity crisis in pharmaceutical R&D.

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Sclerostin: a gem from the genome leads to bone-building antibodies

21 January 2018

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An SCN9A channelopathy causes congenital inability to experience pain

21 January 2018

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Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations

21 January 2018

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Sodium channelopathies and pain

21 January 2018

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The differential diagnosis of congenital analgesia and other diseases with diminished pain perception in childhood. Case report and review

21 January 2018

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No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V.

21 January 2018

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Congenital insensitivity to pain: an update

21 January 2018

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Congenital insensitivity to pain. A clinical, genetic and neurophysiological study of four children from the same family

21 January 2018

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Hereditary sensory and autonomic neuropathies: types II, III, and IV

21 January 2018

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Recent advances in hereditary sensory and autonomic neuropathies

21 January 2018

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Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis

21 January 2018

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21 January 2018

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

21 January 2018

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Familial pain syndromes from mutations of the NaV1.7 sodium channel

21 January 2018

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Natural history of erythromelalgia: presentation and outcome in 168 patients

21 January 2018

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Incidence of erythromelalgia: a population-based study in Olmsted County, Minnesota

21 January 2018

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Severe case and literature review of primary erythromelalgia: novel SCN9A gene mutation

21 January 2018

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Pediatric erythromelalgia: a retrospective review of 32 cases evaluated at Mayo Clinic over a 37-year period

21 January 2018

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Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders

21 January 2018

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A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia

21 January 2018

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Compound heterozygosity in sodium channel Nav1.7 in a family with hereditary erythermalgia

21 January 2018

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

21 January 2018

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Erythromelalgia: new theories and new therapies

21 January 2018

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Channelopathies: a review

21 January 2018

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SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes

21 January 2018

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The diagnostic criteria for small fibre neuropathy: from symptoms to neuropathology

21 January 2018

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Diagnosis and treatment of pain in small-fiber neuropathy

21 January 2018

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Small fiber neuropathy: is skin biopsy the holy grail?

21 January 2018

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Gain of function NaV1.7 mutations in idiopathic small fiber neuropathy

21 January 2018

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Treatment of Na(v)1.7-mediated pain in inherited erythromelalgia using a novel sodium channel blocker

21 January 2018

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Pain perception is altered by a nucleotide polymorphism in SCN9A

21 January 2018

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Contribution of genetic variants to pain susceptibility in Parkinson disease

21 January 2018

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Nociceptor-specific gene deletion reveals a major role for Nav1.7 (PN1) in acute and inflammatory pain

21 January 2018

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Distinct Nav1.7-dependent pain sensations require different sets of sensory and sympathetic neurons

21 January 2018

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