J. M�ller-H�cker

Author

J. M�ller-H�cker

Ludwig-Maximilians-Universität München

Also Known As

J. M�ller-H�cker, Josef M�ller-H�cker

Publications

565

Citations

H-Index

Concepts

All Affiliations

Ludwig-Maximilians-Universität München Friedrich Baur Stiftung München Klinik Schwabing

About

J. M�ller-H�cker is an author at Ludwig-Maximilians-Universität München specializing in medicine, pathology, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	455
2	Biochemistry	2	2	169
3	Health Sciences	1	1	27
4	Applied Physiology	1	1	27
5	Biology	1	1	34

J. M�ller-H�cker

Publications

482

Citations

H-Index

Page 1

	Year	Citations
Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome H. S. A. Heymans, H. van den Bosch, R. B. H. Schutgens, European Journal of Pediatrics Glomerular DiseaseHepatologyMedicineKidney FailureHematology	1984	88
Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine J. M�ller-H�cker, D. Pongratz, Thomas Deufel, Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin BiochemistryPhysiologyInherited Metabolic DiseaseMetabolismMedicine	1982	88
Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia J. M�ller-H�cker, D. Pongratz, G. H�bner Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin Ocular DiseaseBiochemistryOphthalmologySkeletal MusclePhysiology	1983	81
Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes Klaus-Dieter Gerbitz, B. Obermaier–Kusser, S. Zierz, Journal of Neurology Mitochondrial MyopathyMendelian DisorderMitochondrial FunctionGeneticsPathology	1990	58
Fatal copper storage disease of the liver in a German infant resembling Indian childhood cirrhosis J. M�ller-H�cker, Michael Wei�, Ulrike Meyer, Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin Hepatic DisordersHepatologyIndian Childhood CirrhosisPediatricsHepatitis	1987	51
Variable reduction of caveolin-3 in patients with LGMD2B/MM Maggie C. Walter, Christian Braun, Matthias Vorgerd, Journal of Neurology Translational MedicineDegenerative DiseaseVariable ReductionPharmacotherapyMedicine	2003	44
A specific point mutation in the mitochondrial genome of Caucasians with MELAS C. Enter, J. M�ller-H�cker, S. Zierz, Human Genetics BiologySpecific Point MutationComparative GenomicsGeneticsMedicine	1991	34
Exercise-induced myalgia in hypothyroidism Hanns Lochm�ller, C. D. Reimers, Peter Fischer, Journal of Molecular Medicine ExerciseExercise PhysiologyPhysiologyPhysical ExerciseApplied Physiology	1993	27
Adenoma of the middle ear mucosa B.J. Arnold, C Zietz, J. M�ller-H�cker, European Archives of Oto-Rhino-Laryngology Surgical PathologyOtorhinolaryngologyPathologyNeurotologyMedicine	1996	11

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