(Q37150552)

18 August 2017

Advanced Genetic Testing Comes to the Pain Clinic to Make a Diagnosis of Paroxysmal Extreme Pain Disorder (English)

1 reference

18 August 2017

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27525141%20AND%20SRC:MED&resulttype=core&format=json

Douglas L Riegert-Johnson

12 June 2020

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27525141%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

author name string

Ashley Cannon

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27525141%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Kimberly J Guthrie

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27525141%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

publication date

21 July 2016

1 reference

Case Reports in Neurological Medicine

18 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27525141%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

volume

2016

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27525141%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

page(s)

9212369

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27525141%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

12 June 2020

copyright license

start time

1 January 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

Novel SCN9A mutations underlying extreme pain phenotypes: unexpected electrophysiological and clinical phenotype correlations

1 reference

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p.L1612P, a novel voltage-gated sodium channel Nav1.7 mutation inducing a cold sensitive paroxysmal extreme pain disorder.

6 September 2017

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Painful neuropathies: the emerging role of sodium channelopathies

6 September 2017

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Inherited pain: sodium channel Nav1.7 A1632T mutation causes erythromelalgia due to a shift of fast inactivation.

6 September 2017

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The Na(V)1.7 sodium channel: from molecule to man.

6 September 2017

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Infrequent SCN9A mutations in congenital insensitivity to pain and erythromelalgia.

6 September 2017

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Gain-of-function Nav1.8 mutations in painful neuropathy.

6 September 2017

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A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia

6 September 2017

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Intra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7.

6 September 2017

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

6 September 2017

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Pain disorders and erythromelalgia caused by voltage-gated sodium channel mutations

6 September 2017

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

6 September 2017

1 reference

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Diagnosis and treatment of pain in small-fiber neuropathy

6 September 2017

1 reference

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Pathology and functional diagnosis of small-fiber painful neuropathy.

6 September 2017

1 reference

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Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)

6 September 2017

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

6 September 2017

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Na(V)1.7 mutant A863P in erythromelalgia: effects of altered activation and steady-state inactivation on excitability of nociceptive dorsal root ganglion neurons.

6 September 2017

1 reference

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What's in a name--familial rectal pain syndrome becomes paroxysmal extreme pain disorder

6 September 2017

1 reference

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

6 September 2017

1 reference

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Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7.

6 September 2017

1 reference

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Expression of alternatively spliced sodium channel alpha-subunit genes. Unique splicing patterns are observed in dorsal root ganglia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Rectal, ocular, and submaxillary pain; a familial autonomic disorder related to proctalgia fugaz: report of a family

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Wind-up of spinal cord neurones and pain sensation: much ado about something?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Slow sodium conductances of dorsal root ganglion neurons: intraneuronal homogeneity and interneuronal heterogeneity

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

The induction and maintenance of central sensitization is dependent on N -methyl-d-aspartic acid receptor activation; implications for the treatment of post-injury pain hypersensitivity states

6 September 2017

1 reference

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Hyperalgesia mediated by spinal glutamate or substance P receptor blocked by spinal cyclooxygenase inhibition

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Gain-of-function mutations in sodium channel Na(v)1.9 in painful neuropathy

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Small-fiber neuropathy Nav1.8 mutation shifts activation to hyperpolarized potentials and increases excitability of dorsal root ganglion neurons.

3 September 2018

1 reference

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Small nerve fibres, small hands and small feet: a new syndrome of pain, dysautonomia and acromesomelia in a kindred with a novel NaV1.7 mutation.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Paroxysmal extreme pain disorder: a molecular lesion of peripheral neurons

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Early- and late-onset inherited erythromelalgia: genotype-phenotype correlation.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Characterization of a familial case with primary erythromelalgia from Taiwan.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Characterization of the glutamatergic system for induction and maintenance of allodynia.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

Development and preliminary validation of a pain measure specific to neuropathic pain: the Neuropathic Pain Scale

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4972908

A case of primary erythermalgia, wintry hypothermia and encephalopathy

3 September 2018

1 reference

12 December 2020

The G1662S NaV1.8 mutation in small fibre neuropathy: impaired inactivation underlying DRG neuron hyperexcitability

1 reference

12 December 2020

1 reference

12 December 2020

Diagnostic clinical genome and exome sequencing

1 reference

12 December 2020

Long-term study on the effects of visual biofeedback and muscle training as a therapeutic modality in pelvic floor dyssynergia and slow-transit constipation

1 reference

12 December 2020

Identifiers

DOI

10.1155/2016/9212369

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27525141%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27525141%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

1 reference