Emerging role of the KCNT1 Slack channel in intellectual disability (Q33958421)

30 July 2017

title

Emerging role of the KCNT1 Slack channel in intellectual disability (English)

1 reference

30 July 2017

0 references

intellectual disability

1 reference

disability affecting intellectual abilities

inferred from title

1 reference

Grace E Kim

1

1 reference

30 July 2017

Leonard K Kaczmarek

series ordinal

2

1 reference

30 July 2017

publication date

28 July 2014

1 reference

Frontiers in Cellular Neuroscience

30 July 2017

published in

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30 July 2017

volume

8

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30 July 2017

page(s)

209

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Epilepsy among children and adolescents with autism spectrum disorders: a population-based study.

30 July 2017

cites work

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Epilepsy and EEG findings in males with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Autosomal dominant nocturnal frontal lobe epilepsy: an electroclinical study of a Norwegian family with ten affected members

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

PKA-induced internalization of slack KNa channels produces dorsal root ganglion neuron hyperexcitability

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Successful control with bromide of two patients with malignant migrating partial seizures in infancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

A case of Ohtahara syndrome with mitochondrial respiratory chain complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Voltage-sensing residues in the S2 and S4 segments of the Shaker K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Child neurology: epilepsy of infancy with migrating focal seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Glucose sensitivity of mouse olfactory bulb neurons is conveyed by a voltage-gated potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Malignant migrating partial seizures in infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Sodium-dependent potassium channels of a Slack-like subtype contribute to the slow afterhyperpolarization in lamprey spinal neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Slack and Slick K(Na) channels regulate the accuracy of timing of auditory neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4112808

Properties and rundown of sodium-activated potassium channels in rat olfactory bulb neurons

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4112808

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

29 October 2018

1 reference

https://api.crossref.org/works/10.3389%2FFNCEL.2014.00209

Autism spectrum disorder in fragile X syndrome: a longitudinal evaluation

21 January 2018

1 reference

12 December 2020

Paternal mosaicism of an STXBP1 mutation in OS

1 reference

12 December 2020

Zonisamide treatment of early infantile epileptic encephalopathy

1 reference

12 December 2020

A case of Ohtahara syndrome with olivary-dentate dysplasia and agenesis of mamillary bodies

1 reference

12 December 2020

Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome

1 reference

12 December 2020

Familial Ohtahara syndrome due to a novel ARX gene mutation

1 reference

12 December 2020

Suppression-burst patterns in intractable epilepsy with focal cortical dysplasia

1 reference

12 December 2020

Early infantile epileptic encephalopathy with suppression burst: Ohtahara syndrome

1 reference

12 December 2020

Formation of intermediate-conductance calcium-activated potassium channels by interaction of Slack and Slo subunits

1 reference

12 December 2020

Impact of early hemispherotomy in a case of Ohtahara syndrome with left parieto-occipital megalencephaly

1 reference

12 December 2020

Epilepsy surgery for early infantile epileptic encephalopathy (ohtahara syndrome)

1 reference

12 December 2020

Association of genomic deletions in the STXBP1 gene with Ohtahara syndrome

1 reference

12 December 2020

STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern

1 reference

12 December 2020

Identifiers

DOI

10.3389/FNCEL.2014.00209

1 reference

30 July 2017

1 reference

30 July 2017

1 reference