(Q34625827)

3 August 2017

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title

Mitochondria and neonatal epileptic encephalopathies with suppression burst (English)

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3 August 2017

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Florence Molinari

1

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3 August 2017

publication date

1 December 2010

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Journal of Bioenergetics and Biomembranes

3 August 2017

published in

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3 August 2017

volume

42

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3 August 2017

issue

6

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3 August 2017

page(s)

467-471

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Opposing role of synaptic and extrasynaptic NMDA receptors in regulation of the extracellular signal-regulated kinases (ERK) activity in cultured rat hippocampal neurons

3 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10863-010-9323-6

GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis

21 January 2018

1 reference

12 December 2020

Bovine complex I is a complex of 45 different subunits.

1 reference

12 December 2020

1 reference

12 December 2020

The mitochondrial transporter family (SLC25): physiological and pathological implications

1 reference

12 December 2020

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

1 reference

12 December 2020

Prognosis in Childhood Epilepsy: A Prospective Follow-Up Study

1 reference

12 December 2020

Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy

1 reference

12 December 2020

Frameshift mutations of the ARX gene in familial Ohtahara syndrome

1 reference

12 December 2020

Respiratory chain complex I deficiency in an infant with Ohtahara syndrome.

1 reference

12 December 2020

Glutamate acting at NMDA receptors stimulates embryonic cortical neuronal migration

1 reference

12 December 2020

Mitochondrial transport proteins of the brain

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12 December 2020

Glutamate enhances the surface distribution and release of Munc18 in cerebral cortical neurons

1 reference

12 December 2020

Synaptic assembly of the brain in the absence of neurotransmitter secretion

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12 December 2020

Autoimmunity to munc-18 in Rasmussen's encephalitis.

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of the mitochondrial glutamate transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms

1 reference

12 December 2020

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

1 reference

12 December 2020

Inactivation of Arx, the murine ortholog of the X-linked lissencephaly with ambiguous genitalia gene, leads to severe disorganization of the ventral telencephalon with impaired neuronal migration and differentiation

1 reference

12 December 2020

The presynaptic CaV2.2 channel-transmitter release site core complex

1 reference

12 December 2020

Infantile epileptic syndromes and metabolic etiologies

1 reference

12 December 2020

A novel ARX phenotype: rapid neurodegeneration with Ohtahara syndrome and a dyskinetic movement disorder.

1 reference

12 December 2020

A case of Ohtahara syndrome with cytochrome oxidase deficiency

1 reference

12 December 2020

Mitochondrial disorders in the nervous system

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12 December 2020

A noncanonical release of GABA and glutamate modulates neuronal migration.

1 reference

12 December 2020

Age‐Dependent Epileptic Encephalopathy: a Longitudinal Study

1 reference

12 December 2020

Epileptic encephalopathies in early infancy with suppression-burst

1 reference

12 December 2020

Mitochondrial metabolite carrier proteins: purification, reconstitution, and transport studies

1 reference

12 December 2020

Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesis

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12 December 2020

Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts

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12 December 2020

Extrasynaptic NMDARs oppose synaptic NMDARs by triggering CREB shut-off and cell death pathways

1 reference

12 December 2020

A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome)

1 reference

12 December 2020

Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X).

1 reference

12 December 2020

10.1007/S10863-010-9323-6

Identifiers

DOI

1 reference

Dimensions Publication ID

3 August 2017

1045689964

0 references

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