(Q67208792)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Clinical heterogeneity in respiratory chain complex III deficiency in childhood (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

J Mourmans

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

U Wendel

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

H A Bentlage

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

J M Trijbels

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

J A Smeitink

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

I F de Coo

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

F J Gabreëls

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

R C Sengers

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

W Ruitenbeek

9

1 reference

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3 November 2019

publication date

1 July 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

Journal of the Neurological Sciences

3 November 2019

number of pages

7

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

149

1 reference

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3 November 2019

issue

1

1 reference

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3 November 2019

page(s)

111-117

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

Gene structure and cell type-specific expression of the human ATP synthase alpha subunit

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Human diseases with defects in oxidative phosphorylation. 1. Decreased amounts of assembled oxidative phosphorylation complexes in mitochondrial encephalomyopathies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Fatal lactic acidosis in infancy with a defect of complex III of the respiratory chain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Decreased expression of ubiquinol-cytochrome c reductase subunits in patients exhibiting mitochondrial myopathy with progressive exercise intolerance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Mitochondrial myopathy: tissue-specific expression of a defect in ubiquinol-cytochrome c reductase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Enzymological versus DNA investigations in mitochondrial (encephalo‐)myopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

7 January 2021

Mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Cytochrome c oxidase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

A new mitochondrial myopathy. Biochemical studies revealing a deficiency in the cytochrome b-c1 complex (complex III) of the respiratory chain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Defects in the cytochrome bc1 complex in mitochondrial diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Novel mutations in mitochondrial cytochrome b in fatal post partum cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Clinical aspects of mitochondrial disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Mitochondrial myopathies: multiple enzyme defects in the respiratory chain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Biochemical and molecular investigations in respiratory chain deficiencies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Subunit structures of purified beef mitochondrial cytochrome bc1 complex from liver and heart.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Neonatal De Toni-Debré-Fanconi syndrome due to a defect in complex III of the respiratory chain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2897%2905379-3

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-510X(97)05379-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9168175%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference