(Q33437374)

26 July 2017

title

MELAS with A3243G mutation presenting with occipital status epilepticus (English)

1 reference

26 July 2017

1 reference

Shefali Karkare

1

1 reference

26 July 2017

Sabiha Merchant

2

1 reference

26 July 2017

Gail Solomon

3

1 reference

26 July 2017

Murray Engel

4

1 reference

26 July 2017

Barry Kosofsky

5

1 reference

26 July 2017

language of work or name

1 reference

29 April 2009

1 reference

Journal of Child Neurology

26 July 2017

published in

1 reference

26 July 2017

volume

24

1 reference

26 July 2017

issue

12

1 reference

26 July 2017

page(s)

1564-1567

1 reference

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.

26 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Symptomatic occipital lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Childhood occipital epilepsy of Gastaut: a study of 33 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Hippocampal sclerosis and status epilepticus: cause or consequence? A MRI study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Imaging of the epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Mitochondrial respiratory chain defects: underlying etiology in various epileptic conditions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

MELAS with prominent white matter gliosis and atrophy of the cerebellar granular layer: a clinical, genetic, and pathological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Distinguishing ischemic stroke from the stroke-like lesions of MELAS using apparent diffusion coefficient mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Epileptic phenotypes associated with mitochondrial disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

"Erratic" complex partial status epilepticus as a presenting feature of MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Epilepsy and respiratory chain defects in children with mitochondrial encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Mitochondrial DNA mutations and mitochondrial dysfunction in epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809334386

21 January 2018

Identifiers

DOI

10.1177/0883073809334386

1 reference

26 July 2017

1 reference