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Complete failure of insulin-transmitted signaling, but not obesity-induced insulin resistance, impairs respiratory chain function in muscle

Journal of molecular medicine (Berlin, Germany), 2012-10, Vol.90 (10), p.1145-1160

2012

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Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis

Brain (London, England : 1878), 2000-07, Vol.123 (7), p.1339-1348

2000

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Neurobehavioral outcome prediction after cardiac surgery : Role of neurobiochemical markers of damage to neuronal and glial brain tissue

Stroke (1970), 2000-03, Vol.31 (3), p.645-650

2000

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Automated CD61 immunoplatelet analysis of thrombocytopenic samples

British journal of haematology, 2001-03, Vol.112 (3), p.584-592

2001

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Mesial temporal lobe epilepsy associated with KCNT1 mutation

Seizure (London, England), 2017-02, Vol.45, p.181-183

2017

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Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis

Journal of the neurological sciences, 1998, Vol.156 (1), p.65-72

1998

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Mitochondrial dysfunction in neurodegenerative disorders

Biochemical Society transactions, 2007-11, Vol.35 (Pt 5), p.1228

2007

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Re-evaluation of the dysfunction of mitochondrial respiratory chain in skeletal muscle of patients with Parkinson's disease

Journal of Neural Transmission, 2005-04, Vol.112 (4), p.499-518

2005

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Characterization of Superoxide-producing Sites in Isolated Brain Mitochondria

The Journal of biological chemistry, 2004-02, Vol.279 (6), p.4127-4135

2004

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Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis

Journal of the neurological sciences, 1999-10, Vol.169 (1), p.133-139

1999

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Dopamine transporter SPECT in patients with mitochondrial disorders

Journal of neurology, neurosurgery and psychiatry, 2005-01, Vol.76 (1), p.118-120

2005

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Altered mitochondrial oxidative phosphorylation in hippocampal slices of kainate-treated rats

Brain research, 1999-05, Vol.826 (2), p.236-242

1999

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Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene

Neurology, 2010-02, Vol.74 (6), p.507

2010

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Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vivo

Molecular and cellular biochemistry, 1998-07, Vol.184 (1-2), p.81-100

1998

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Primary carnitine deficiency: adult onset lipid storage myopathy with a mild clinical course

Journal of clinical neuroscience, 2004-11, Vol.11 (8), p.919-924

2004

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Mitochondrial complex I deficiency in the epileptic focus of patients with temporal lobe epilepsy

Annals of neurology, 2000-11, Vol.48 (5), p.766-773

2000

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New Insights into the Metabolic Consequences of Large-Scale mtDNA Deletions: A Quantitative Analysis of Biochemical, Morphological, and Genetic Findings in Human Skeletal Muscle

Journal of neuropathology and experimental neurology, 2000-05, Vol.59 (5), p.353-360

2000

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Effect of 1-methyl-4-phenylpyridinium on glutathione in rat pheochromocytoma PC 12 cells

Neurochemistry international, 2000-05, Vol.36 (6), p.489-497

2000

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Large-conductance K+ channel openers induce death of human glioma cells

Journal of physiology and pharmacology : an official journal of the Polish Physiological Society, 2009-12, Vol.60 (4), p.27

2009

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Overexpression of bcl-2 Results in Reduction of Cytochrome c Content and Inhibition of Complex I Activity

Biochemical and biophysical research communications, 2001-02, Vol.280 (4), p.1021-1027

2001

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Different metabolic properties of mitochondrial oxidative phosphorylation in different cell types - important implications for mitochondrial cytopathies

Experimental physiology, 2003-01, Vol.88 (1), p.149-154

Kunz, Wolfram S.

2003

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Functional characterization of mitochondrial oxidative phosphorylation in saponin-skinned human muscle fibers

Biochimica et biophysica acta, 1993-08, Vol.1144 (1), p.46-53

1993

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Phosphate affects the distribution of flux control among the enzymes of oxidative phosphorylation in rat skeletal muscle mitochondria

The Journal of biological chemistry, 1993-05, Vol.268 (13), p.9343-9346

1993

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Potassium channel openers depolarize hippocampal mitochondria

Brain research, 2001-02, Vol.892 (1), p.42-50

2001

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Proof of progression over time: Finally fulminant brain, muscle, and liver affection in Alpers syndrome associated with the A467T POLG1 mutation

Seizure (London, England), 2009-04, Vol.18 (3), p.232-234

2009

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Complete failure of insulin-transmitted signaling, but not obesity-induced insulin resistance, impairs respiratory chain function in muscle

Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis

Neurobehavioral outcome prediction after cardiac surgery : Role of neurobiochemical markers of damage to neuronal and glial brain tissue

Automated CD61 immunoplatelet analysis of thrombocytopenic samples

Mesial temporal lobe epilepsy associated with KCNT1 mutation

Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis

Mitochondrial dysfunction in neurodegenerative disorders

Re-evaluation of the dysfunction of mitochondrial respiratory chain in skeletal muscle of patients with Parkinson's disease

Characterization of Superoxide-producing Sites in Isolated Brain Mitochondria

Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis

Dopamine transporter SPECT in patients with mitochondrial disorders

Altered mitochondrial oxidative phosphorylation in hippocampal slices of kainate-treated rats

Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene

Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vivo

Primary carnitine deficiency: adult onset lipid storage myopathy with a mild clinical course

Mitochondrial complex I deficiency in the epileptic focus of patients with temporal lobe epilepsy

New Insights into the Metabolic Consequences of Large-Scale mtDNA Deletions: A Quantitative Analysis of Biochemical, Morphological, and Genetic Findings in Human Skeletal Muscle

Effect of 1-methyl-4-phenylpyridinium on glutathione in rat pheochromocytoma PC 12 cells

Large-conductance K+ channel openers induce death of human glioma cells

Overexpression of bcl-2 Results in Reduction of Cytochrome c Content and Inhibition of Complex I Activity

Different metabolic properties of mitochondrial oxidative phosphorylation in different cell types - important implications for mitochondrial cytopathies

Functional characterization of mitochondrial oxidative phosphorylation in saponin-skinned human muscle fibers

Phosphate affects the distribution of flux control among the enzymes of oxidative phosphorylation in rat skeletal muscle mitochondria

Potassium channel openers depolarize hippocampal mitochondria

Proof of progression over time: Finally fulminant brain, muscle, and liver affection in Alpers syndrome associated with the A467T POLG1 mutation

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