(Q39536524)

12 September 2017

title

Acute mitochondrial encephalopathy reflects neuronal energy failure irrespective of which genome the genetic defect affects (English)

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12 September 2017

Charalampos Tzoulis

1

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Laurence Bindoff

object named as

Laurence A Bindoff

series ordinal

2

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language of work or name

English

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publication date

12 October 2012

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12 September 2017

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12 September 2017

volume

135

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12 September 2017

issue

Pt 12

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12 September 2017

page(s)

3627-3634

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Oxygen and glucose consumption related to Na+-K+ transport in canine brain

12 September 2017

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21 January 2018

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Diffusion-weighted image and MR spectroscopic analysis of a case of MELAS with repeated attacks

21 January 2018

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Diffusion and perfusion characteristics of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode) in thirteen patients

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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MRI and diffusion-weighted imaging followup of a stroke-like event in a patient with MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Cerebral blood flow and oxygen metabolism before and after a stroke-like episode in patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Mitochondrial DNA mutations affect calcium handling in differentiated neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Pathophysiologic evaluation of MELAS strokes by serially quantified MRS and CASL perfusion images

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Apoptotic and necrotic brain lesions in a fatal case of carbon monoxide poisoning

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Serial diffusion-weighted imaging in a patient with MELAS and presumed cytotoxic oedema

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Phenotypic patterns of MELAS/LS overlap syndrome associated with m.13513G>A mutation, and neuropathological findings in one autopsy case

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

Cerebral cortical laminar necrosis on diffusion-weighted MRI in hypoglycaemic encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWS223

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWS223

1 reference

release_gdwrikc6kzeolbufpdqesqcyaa

12 September 2017

Fatcat ID

0 references

1 reference