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Patients with chronic fatigue syndrome performed worse than controls in a controlled repeated exercise study despite a normal oxidative phosphorylation capacity

Journal of translational medicine, 2010-10, Vol.8 (1), p.93-93, Article 93

2010

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Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I Defect

Frontiers in molecular neuroscience, 2017-10, Vol.10, p.336-336

2017

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Correct assay of complex I activity in human skin fibroblasts by timely addition of rotenone

Clinical chemistry (Baltimore, Md.), 2008-11, Vol.54 (11), p.1921-1922

2008

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Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome

Brain (London, England : 1878), 2013-03, Vol.136 (Pt 3), p.882-890

2013

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Exploratory open label, randomized study of acetyl- and propionylcarnitine in chronic fatigue syndrome

Psychosomatic medicine, 2004-03, Vol.66 (2), p.276-282

2004

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Rupture of silicone gel breast implants and symptoms of pain and fatigue

Journal of rheumatology, 2003-10, Vol.30 (10), p.2263

2003

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Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene

Brain (London, England : 1878), 2011, Vol.134 (Pt 1), p.210-219

2011

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Azithromycin in chronic fatigue syndrome (CFS), an analysis of clinical data

Journal of translational medicine, 2006-08, Vol.4 (1), p.34-34, Article 34

2006

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A novel splice site mutation in neonatal carnitine palmitoyl transferase II deficiency

Journal of human genetics, 2003-01, Vol.48 (1), p.8-13

2003

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Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography

Nucleic acids research, 2000-10, Vol.28 (20), p.E89-89

2000

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Chronic fatigue syndrome and sexual dysfunction

Journal of psychosomatic research, 2004-02, Vol.56 (2), p.199-201

2004

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Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment

Pediatrics (Evanston), 2000-09, Vol.106 (3), p.596-600

2000

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Immunological Phenotyping of Fibroblast Cultures from Patients with a Mitochondrial Respiratory Chain Deficit

Laboratory investigation, 2001-08, Vol.81 (8), p.1069-1077

2001

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Rapid isolation of muscle and heart mitochondria, the lability of oxidative phosphorylation and attempts to stabilize the process in vitro by taurine, carnitine and other compounds

Molecular and cellular biochemistry, 1997-09, Vol.174 (1-2), p.61-66

1997

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Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

American journal of human genetics, 1999-02, Vol.64 (2), p.479-494

1999

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Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families

Neuromuscular disorders : NMD, 1998-06, Vol.8 (5), p.296-304

1998

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Deficiency of the adenine nucleotide translocator in muscle of a patient with myopathy and lactic acidosis : a new mitochondrial defect

Pediatric research, 1993-04, Vol.33 (4), p.412-417

1993

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Chronic fatigue syndrome and sexual dysfunction

Journal of psychosomatic research, 2004-02, Vol.55 (2), p.199-201

2004

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Correct Assay of Complex I Activity in Human Skin Fibroblasts by Timely Addition of Rotenone/In Reply

Clinical chemistry (Baltimore, Md.), 2008-11, Vol.54 (11), p.1921

2008

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Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease

The Journal of pediatrics, 1996-05, Vol.128 (5), p.683-687

1996

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Mitochondrial injury : Lessons from the fialuridine trial

Drug safety, 1997-07, Vol.17 (1), p.1-7

1997

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Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency

Human genetics, 1999-08, Vol.105 (1-2), p.157-161

1999

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Breast implant related disease

Journal of rheumatology, 2004-05, Vol.31 (5), p.1015; author reply 1015

2004

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Effect of lamivudine on morphology and function of mitochondria in patients with chronic hepatitis B

Hepatology (Baltimore, Md.), 1997-07, Vol.26 (1), p.211-215

1997

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A Fatal, Systemic Mitochondrial Disease with Decreased Mitochondrial Enzyme Activities, Abnormal Ultrastructure of the Mitochondria and Deficiency of Heat Shock Protein 60

Biochemical and biophysical research communications, 1993-05, Vol.193 (1), p.146-154

1993

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Patients with chronic fatigue syndrome performed worse than controls in a controlled repeated exercise study despite a normal oxidative phosphorylation capacity

Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I Defect

Correct assay of complex I activity in human skin fibroblasts by timely addition of rotenone

Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome

Exploratory open label, randomized study of acetyl- and propionylcarnitine in chronic fatigue syndrome

Rupture of silicone gel breast implants and symptoms of pain and fatigue

Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene

Azithromycin in chronic fatigue syndrome (CFS), an analysis of clinical data

A novel splice site mutation in neonatal carnitine palmitoyl transferase II deficiency

Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography

Chronic fatigue syndrome and sexual dysfunction

Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment

Immunological Phenotyping of Fibroblast Cultures from Patients with a Mitochondrial Respiratory Chain Deficit

Rapid isolation of muscle and heart mitochondria, the lability of oxidative phosphorylation and attempts to stabilize the process in vitro by taurine, carnitine and other compounds

Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families

Deficiency of the adenine nucleotide translocator in muscle of a patient with myopathy and lactic acidosis : a new mitochondrial defect

Chronic fatigue syndrome and sexual dysfunction

Correct Assay of Complex I Activity in Human Skin Fibroblasts by Timely Addition of Rotenone/In Reply

Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease

Mitochondrial injury : Lessons from the fialuridine trial

Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency

Breast implant related disease

Effect of lamivudine on morphology and function of mitochondria in patients with chronic hepatitis B

A Fatal, Systemic Mitochondrial Disease with Decreased Mitochondrial Enzyme Activities, Abnormal Ultrastructure of the Mitochondria and Deficiency of Heat Shock Protein 60

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