(Q48462967)

11 February 2018

title

Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement (English)

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11 February 2018

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J Betts

1

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11 February 2018

E Jaros

2

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11 February 2018

R H Perry

3

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11 February 2018

A M Schaefer

4

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11 February 2018

R W Taylor

5

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11 February 2018

Z Abdel-All

6

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11 February 2018

R N Lightowlers

7

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11 February 2018

D M Turnbull

8

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11 February 2018

publication date

1 August 2006

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11 February 2018

Neuropathology and Applied Neurobiology

published in

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11 February 2018

volume

32

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11 February 2018

issue

4

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11 February 2018

page(s)

359-373

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11 February 2018

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

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1 reference

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A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

21 January 2018

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Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes

21 January 2018

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Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia

21 January 2018

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Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions

21 January 2018

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Central nervous system changes in mitochondrial encephalomyopathy: light and electron microscopic study

21 January 2018

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

21 January 2018

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Mitochondrial encephalomyopathy with lactic acidosis and stroke like episodes (MELAS) with prominent degeneration of the intestinal wall and cactus-like cerebellar pathology.

21 January 2018

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Mitochondrial respiratory-chain diseases

21 January 2018

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Mutations of the mitochondrial ND1 gene as a cause of MELAS.

21 January 2018

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An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome

21 January 2018

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Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

21 January 2018

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Vascular involvement in mitochondrial myopathy.

21 January 2018

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Adult-onset MELAS. Evidence for involvement of neurons as well as cerebral vasculature in strokelike episodes.

21 January 2018

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The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.

21 January 2018

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Methods of microphotometric assay of succinate dehydrogenase and cytochrome c oxidase activities for use on human skeletal muscle.

21 January 2018

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Senile dementia of Lewy body type. A clinically and neuropathologically distinct form of Lewy body dementia in the elderly

21 January 2018

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Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age.

21 January 2018

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Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.

21 January 2018

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MELAS: clinical phenotype and morphological brain abnormalities

21 January 2018

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Involvement of choroid plexus in mitochondrial encephalomyopathy (MELAS).

21 January 2018

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Neuropathological features of mitochondrial disorders

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

Cerebral lactic acidosis correlates with neurological impairment in MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

Reversible brain dysfunction in MELAS: MEG, and (1)H MRS analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

Sequencing and quantitative assessment of mutant and wild-type mitochondrial DNA in paraffin sections from cases of MELAS.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

MELAS: clinical features, biochemistry, and molecular genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

Mechanisms of migraine aura revealed by functional MRI in human visual cortex

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

Focal hyperemia followed by spreading oligemia and impaired activation of rcbf in classic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2006.00731.X

10.1111/J.1365-2990.2006.00731.X

21 January 2018

Identifiers

DOI

1 reference

11 February 2018

1 reference

11 February 2018