(Q24200432)

3

object named as

Douglass M Turnbull

0 references

Gerald Pfeffer

1

object named as

Gerald Pfeffer

0 references

author name string

Kari Majamaa

2

0 references

David Thorburn

Cochrane Database of Systematic Reviews

4

0 references

language of work or name

English

0 references

publication date

18 April 2012

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published in

0 references

page(s)

CD004426

0 references

issue

4

0 references

cites work

Dichloroacetate therapy attenuates the blood lactate response to submaximal exercise in patients with defects in mitochondrial energy metabolism

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

A randomized trial of coenzyme Q10 in mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Dichloroacetate causes toxic neuropathy in MELAS: a randomized, controlled clinical trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

A placebo-controlled crossover trial of creatine in mitochondrial diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Creatine has no beneficial effect on skeletal muscle energy metabolism in patients with single mitochondrial DNA deletions: a placebo-controlled, double-blind 31P-MRS crossover study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

The effect of short-term dimethylglycine treatment on oxygen consumption in cytochrome oxidase deficiency: a double-blind randomized crossover clinical trial.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Oxidative stress biomarkers in mitochondrial myopathies, basally and after cysteine donor supplementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Beneficial effects of creatine, CoQ10, and lipoic acid in mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Controlled clinical trial of dichloroacetate for treatment of congenital lactic acidosis in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trial.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

L-arginine improves the symptoms of strokelike episodes in MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Evaluation of long-term treatment of children with congenital lactic acidosis with dichloroacetate

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Sequence and organization of the human mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Chronic treatment of mitochondrial disease patients with dichloroacetate

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Clinical features, investigation, and management of patients with defects of mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Genetic counseling and prenatal diagnosis for mtDNA disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Epidemiology and treatment of mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Nuclear power and mitochondrial disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mitochondrial DNA mutations in human disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mitochondrial respiratory-chain diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Phosphorus magnetic resonance spectroscopy in the evaluation of mitochondrial myopathies: results of a 6-month therapy study with coenzyme Q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mitochondrial myopathies: developments in treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Role of adenine nucleotide translocator 1 in mtDNA maintenance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Therapy of complex I deficiency: peripheral neuropathy during dichloroacetate therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mitochondrial respiratory chain disorders I: mitochondrial DNA defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Remission of Leber's hereditary optic neuropathy with idebenone

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Do idebenone and vitamin therapy shorten the time to achieve visual recovery in Leber hereditary optic neuropathy?

21 January 2018

2 references

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

21 January 2018

12 December 2020

Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Dichloroacetate treatment for mitochondrial cytopathy: long-term effects in MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Respiratory chain complex III [correction of complex] in deficiency with pruritus: a novel vitamin responsive clinical feature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Resistance training in patients with single, large-scale deletions of mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Familial cerebellar ataxia with muscle coenzyme Q10 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Successful treatment with succinate in a patient with MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Effect of high-dose vitamins, coenzyme Q and high-fat diet in paediatric patients with mitochondrial diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

MELAS syndrome with mitochondrial tRNA(Leu)(UUR) mutation: correlation of clinical state, nerve conduction, and muscle 31P magnetic resonance spectroscopy during treatment with nicotinamide and riboflavin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Ubiquinone and nicotinamide treatment of patients with the 3243A-->G mtDNA mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Prevalence of mitochondrial DNA disease in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

21 January 2018

Mitochondrial disease

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mitochondrial DNA mutations and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mitochondrial diseases: a cross-talk between mitochondrial and nuclear genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Creatine monohydrate increases strength in patients with neuromuscular disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Recent advances in the genetics of mitochondrial encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mitochondrial DNA mutations in diseases of energy metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mitochondrial diseases in man and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Mitochondrial fusion and fission in cell life and death

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Pathogenic mutations of nuclear genes associated with mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Treatment for mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F14651858.CD004426.PUB3

Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects

21 January 2018

1 reference

12 December 2020

Marked reduction in CSF lactate and pyruvate levels after CoQ therapy in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)

1 reference

12 December 2020

Metabolic interventions against complex I deficiency in MELAS syndrome

1 reference

12 December 2020

Effect of coenzyme Q10 in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): evaluation by noninvasive tissue oximetry

1 reference

12 December 2020

Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency

1 reference

12 December 2020

Effects of aerobic training in patients with mitochondrial myopathies

1 reference

12 December 2020

Treatment of complex I deficiency with riboflavin

1 reference

12 December 2020

Mitochondrial damage in patients with long-term corticosteroid therapy: development of oculoskeletal symptoms similar to mitochondrial disease

1 reference

12 December 2020

Long-term coenzyme Q10 therapy for a mitochondrial encephalomyopathy with cytochrome c oxidase deficiency: a 31P NMR study

1 reference

12 December 2020

Mitochondrial encephalomyopathy with coenzyme Q10 deficiency

1 reference

12 December 2020

Mitochondrial encephalomyopathy with corticosteroid dependence

1 reference

12 December 2020

Short-term dichloroacetate treatment improves indices of cerebral metabolism in patients with mitochondrial disorders

1 reference

12 December 2020

Treatment of Kearns-Sayre syndrome with coenzyme Q10

1 reference

12 December 2020

Exercise intolerance in mitochondrial myopathy is not related to lactic acidosis

1 reference

12 December 2020

Fatal metabolic acidosis, hyperglycemia, and coma after steroid therapy for Kearns-Sayre syndrome

1 reference

12 December 2020

Variable distribution of mutant mitochondrial DNAs (tRNA(Leu[3243])) in tissues of symptomatic relatives with MELAS: the role of mitotic segregation

1 reference

12 December 2020

The influence of coenzyme Q10 on total serum calcium concentration in two patients with kearns-sayre syndrome and hypoparathyroidism

1 reference

12 December 2020

Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies

1 reference

12 December 2020

CPEO and carnitine deficiency overlapping in MELAS syndrome.

1 reference

12 December 2020

Mitochondrial encephalomyopathy (MELAS): pathological study and successful therapy with coenzyme Q10 and idebenone

1 reference

12 December 2020

Correction of increased plasma pyruvate and plasma lactate levels using large doses of thiamine in patients with Kearns-Sayre syndrome

1 reference

12 December 2020

Coenzyme Q10 treatment in mitochondrial encephalomyopathies. Short-term double-blind, crossover study

1 reference

12 December 2020

A randomized, controlled trial of creatine monohydrate in patients with mitochondrial cytopathies

1 reference

12 December 2020

Exercise training in mitochondrial myopathy: a randomized controlled trial

1 reference

12 December 2020

31P NMR spectroscopy and ergometer exercise test as evidence for muscle oxidative performance improvement with coenzyme Q in mitochondrial myopathies

1 reference

12 December 2020

10.1002/14651858.CD004426.PUB3

Identifiers

DOI

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ei4fhki4kzg3fdocnw7olmlvym

30 July 2022

release_ei4fhki4kzg3fdocnw7olmlvym

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ei4fhki4kzg3fdocnw7olmlvym

30 July 2022

OpenCitations bibliographic resource ID

1892057

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

https://api.fatcat.wiki/v0/release/ei4fhki4kzg3fdocnw7olmlvym

30 July 2022

https://api.fatcat.wiki/v0/release/ei4fhki4kzg3fdocnw7olmlvym

1 reference

30 July 2022