Biomarkers for mitochondrial respiratory chain disorders (Q37799755)

23 August 2017

title

Biomarkers for mitochondrial respiratory chain disorders (English)

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23 August 2017

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Anu Suomalainen

1

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23 August 2017

publication date

13 October 2010

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Journal of Inherited Metabolic Disease

23 August 2017

published in

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23 August 2017

volume

34

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23 August 2017

issue

2

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23 August 2017

page(s)

277-282

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Ketogenic diet slows down mitochondrial myopathy progression in mice

23 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Data integration in plant biology: the O2PLS method for combined modeling of transcript and metabolite data

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Biochemical parameters for the diagnosis of mitochondrial respiratory chain deficiency in humans, and their lack of age-related changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Proteomics approaches to study genetic and metabolic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

The in-depth evaluation of suspected mitochondrial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Infantile onset spinocerebellar ataxia with sensory neuropathy: a new inherited disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Cerebral oxygen and glucose metabolism in patients with mitochondrial m.3243A>G mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Five new cases of a recently described leukoencephalopathy with high brain lactate

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

A plasma signature of human mitochondrial disease revealed through metabolic profiling of spent media from cultured muscle cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Minimum birth prevalence of mitochondrial respiratory chain disorders in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

A new leukoencephalopathy with brainstem and spinal cord involvement and high lactate

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Mitochondrial disorders: a proposal for consensus diagnostic criteria in infants and children

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9222-3

Methods for the differential integrative omic analysis of plasma from a transgenic disease animal model

21 January 2018

1 reference

12 December 2020

PET tracers for the peripheral benzodiazepine receptor and uses thereof

1 reference

12 December 2020

Mitochondrial myopathy induces a starvation-like response

1 reference

12 December 2020

Marked elevation of the chemokine CCL18/PARC in Gaucher disease: a novel surrogate marker for assessing therapeutic intervention

1 reference

12 December 2020

10.1007/S10545-010-9222-3

Identifiers

DOI

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23 August 2017

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