Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features (Q71939979)

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scientific article published on 01 November 1996

Language	Label	Description	Also known as
English	Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features	scientific article published on 01 November 1996

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8981296%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Mitochondrial encephalopathy with multiple mitochondrial DNA deletions: a report of two families and two sporadic cases with unusual clinical and neuropathological features (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8981296%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

John A. Morgan-Hughes

5

object named as

J A Morgan-Hughes

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22 October 2019

author name string

R M Chalmers

1

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22 October 2019

M Brockington

2

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22 October 2019

R S Howard

3

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22 October 2019

B R Lecky

4

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22 October 2019

A E Harding

6

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22 October 2019

publication date

1 November 1996

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22 October 2019

number of pages

5

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Journal of the Neurological Sciences

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22 October 2019

143

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22 October 2019

1-2

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22 October 2019

41-45

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22 October 2019

Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA

1 reference

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7 January 2021

Familial mitochondrial myopathy associated with peripheral neuropathy: partial deficiencies of complex I and complex IV

1 reference

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7 January 2021

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

1 reference

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7 January 2021

Mitochondrial DNA deletions in inherited recurrent myoglobinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROME

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

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7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

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7 January 2021

Chronic demyelinating neuropathy associated with benign IgM paraproteinaemia

1 reference

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7 January 2021

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

An autosomal locus predisposing to deletions of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900032-9

7 January 2021

Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies

1 reference

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7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

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7 January 2021

Identifiers

10.1016/S0022-510X(96)00032-9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8981296%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8981296%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

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