Jürgen‐Christoph von Kleist-Retzow

Author

Also Known As

Jurgen-Christoph von Kleist-Retzow, Jurgen‐Christoph Von Kleist‐Retzow, Jürgen-Christoph Von Kleist-Retzow, Jürgen-Christoph von Kleist-Retzow, Jürgen-Christoph von Kleist-Retzow, Jürgen‐Christoph Von Kleist‐Retzow, Jürgen‐Christoph von Kleist-Retzow, Jürgen‐Christoph von Kleist‐Retzow, Von Kleist-Retzow, Jürgen-Christoph

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

University of Cologne Inserm University Hospital Cologne Hôpital des Enfants Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases

About

Jürgen‐Christoph von Kleist-Retzow is an author at University of Cologne specializing in medicine, mitochondrial function, and oxidative stress.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	19	2K
2	Natural Sciences	3	3	113
3	Engineering	1	1	44
4	Health Sciences	1	1	63
5	Public Health	1	1	15

Jürgen‐Christoph von Kleist-Retzow

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Prohibitins control cell proliferation and apoptosis by regulating OPA1-dependent cristae morphogenesis in mitochondria Carsten Merkwirth, Sascha Dargazanli, Takashi Tatsuta, Genes & Development Opa1-dependent Cristae MorphogenesisMitophagyMurine Phb2Developmental BiologySignal Transduction	2008	529
Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary study Pierre Rustin, Jürgen‐Christoph von Kleist-Retzow, Karine Chantrel-Groussard, The Lancet CardiomyopathyHeart FailureCardiovascular DiseaseMedicineNeurology	1999	350
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome Hélène De Leersnyder, Marie‐Christine de Blois, Bruno Claustrat, The Journal of Pediatrics ChronobiologyMedicinePineal GlandCircadian RhythmSmith-magenis Syndrome	2001	185
Antenatal manifestations of mitochondrial respiratory chain deficiency Jürgen‐Christoph von Kleist-Retzow, Valérie Cormier‐Daire, Géraldine Viot, The Journal of Pediatrics Mitochondrial BiogenesisMitochondrial FunctionPhysiologyPediatricsMaternal Health	2003	133
Targeted disruption of hepatic frataxin expression causes impaired mitochondrial function, decreased life span and tumor growth in mice René Thierbach, Tim J. Schulz, Frank Isken, Human Molecular Genetics	2005	127
Recessive TRAPPC11 Mutations Cause a Disease Spectrum of Limb Girdle Muscular Dystrophy and Myopathy with Movement Disorder and Intellectual Disability Nina Bögershausen, Nassim Shahrzad, Jessica X. Chong, The American Journal of Human Genetics Genetic DisorderMedicineGeneticsPathologyDisease Spectrum	2013	118
Mosaic Deficiency in Mitochondrial Oxidative Metabolism Promotes Cardiac Arrhythmia during Aging Olivier R. Baris, Stefan Ederer, Johannes Neuhaus, Cell Metabolism Cardiac MuscleCardiomyopathyHeart FailureMitochondrial FunctionBiochemistry	2015	91
A High Rate (20%–30%) of Parental Consanguinity in Cytochrome-Oxidase Deficiency Jürgen‐Christoph von Kleist-Retzow, Valérie Cormier‐Daire, Pascale de Lonlay, The American Journal of Human Genetics BiochemistryHeme HomeostasisIron MetabolismGeneticsCytochrome-oxidase Deficiency	1998	82
Acute liver failure with subsequent cirrhosis as the primary manifestation of <i>TRMU</i> mutations Ulrike Schara, Jürgen‐Christoph von Kleist-Retzow, Elke Lainka, Journal of Inherited Metabolic Disease	2010	68
Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies Saskia J.G. Hoefs, Ola H. Skjeldal, Richard J. Rodenburg, Molecular Genetics and Metabolism Human ComplexGenome InstabilityGenetic DisorderGeneticsNovel Mutations	2010	68

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