F. Wiedemann

发表

Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples.

C. Elger, W. Kunz, S. Vielhaber, 2000, Analytical biochemistry.

Hypoxia Increases Activity of the BK-Channel in the Inner Mitochondrial Membrane and Reduces Activity of the Permeability Transition Pore

G. Haddad, X. Gu, P. Bednarczyk, 2008, Cellular Physiology and Biochemistry.

The neurotrophin receptor TrkB is colocalized to mitochondrial membranes.

C. Mawrin, K. Dietzmann, D. Siemen, 2006, The international journal of biochemistry & cell biology.

Oxygen dependence of flux control of cytochrome c oxidase – implications for mitochondrial diseases

W. Kunz, F. Wiedemann, 1998, FEBS letters.

Single-cell analysis of mtDNA deletion levels in sporadic amyotrophic lateral sclerosis

B. Bogerts, R. Schneider-Stock, C. Mawrin, 2004, Neuroreport.

Effect of coenzyme Q10 on the mitochondrial function of skin fibroblasts from Parkinson patients

W. Kunz, C. Wallesch, F. Wiedemann, 2004, Journal of the Neurological Sciences.

Detection of Respiratory Chain Defects in Cultivated Skin Fibroblasts and Skeletal Muscle of Patients with Parkinson's Disease

W. Kunz, C. Wallesch, F. Wiedemann, 1999, Annals of the New York Academy of Sciences.

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

C. Elger, H. Heinze, W. Schubert, 2000, Brain : a journal of neurology.

Impaired mitochondrial oxidative phosphorylation in skeletal muscle of the dystrophin-deficient mdx mouse

K. Dietzmann, W. Kunz, A. Kuznetsov, 1998, Molecular and Cellular Biochemistry.

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

W. Kunz, V. Saks, P. Sikk, 1998 .

Complement-associated neuronal loss in a patient with CASPR2 antibody–associated encephalitis

H. Heinze, W. Brück, C. Bien, 2015, Neurology: Neuroimmunology & Neuroinflammation.

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

W. Kunz, P. Sikk, V. Veksler, 2004, Molecular and Cellular Biochemistry.

Mitochondrial DNA and respiratory chain function in spinal cords of ALS patients

E. Schon, M. Beal, C. Mawrin, 2002, Journal of neurochemistry.

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

C. Mawrin, E. Kirches, K. Dietzmann, 2005, Journal of Neural Transmission.

Unusual presentations of patients with the mitochondrial MERRF mutation A8344G

C. Mawrin, E. Kirches, C. Wallesch, 2008, Clinical Neurology and Neurosurgery.

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

W. Kunz, A. Kuznetsov, S. Vielhaber, 1998, Journal of the Neurological Sciences.

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

C. Elger, H. Reichmann, T. Klockgether, 2000, Journal of neuropathology and experimental neurology.

Use of saponin‐permeabilized muscle fibers for the diagnosis of mitochondrial diseases

W. Kunz, F. Wiedemann, K. Winkler, 1998, BioFactors.

Assessment of tumor cell invasion factors in gliomatosis cerebri

B. Sellhaus, A. von Deimling, C. Mawrin, 2005, Journal of Neuro-Oncology.

Analysis of a single nucleotide polymorphism in codon 388 of the FGFR4 gene in malignant gliomas.

B. Bogerts, S. Kropf, C. Mawrin, 2006, Cancer letters.

Is there mitochondrial dysfunction in amyotrophic lateral sclerosis skeletal muscle?

C. Elger, H. Heinze, A. Kudin, 2003, Annals of neurology.

Hypoxia Increases Activity of the BK-Channel in the Inner Mitochondrial Membrane and Reduces Activity of the Permeability Transition Pore

G. Haddad, X. Gu, P. Bednarczyk, 2008, Cellular Physiology and Biochemistry.