J. M�ller-H�cker
Ludwig-Maximilians-Universität München(DE)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Mitochondrial Function and Pathology, ATP Synthase and ATPases Research, Peroxisome Proliferator-Activated Receptors, Thyroid Disorders and Treatments
Most-Cited Works
- → Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine(1982)88 cited
- → Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome(1984)88 cited
- → Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia(1983)81 cited
- → Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes(1990)58 cited
- → Mutations of mitochondrial DNA and human death(1990)51 cited
- → Fatal copper storage disease of the liver in a German infant resembling Indian childhood cirrhosis(1987)51 cited
- → Variable reduction of caveolin-3 in patients with LGMD2B/MM(2003)44 cited
- → A specific point mutation in the mitochondrial genome of Caucasians with MELAS(1991)34 cited
- → Exercise-induced myalgia in hypothyroidism(1993)27 cited
- → Zur Morphologie und Diagnostik des Zellweger Syndroms(1981)27 cited