Author

Klaus E. Gempel

Observed names: Gempel, Klaus, K Gempel, K. Gempel, Klaus Gempel

Observed institutions: Universität Hamburg, University of Freiburg, Heidelberg University, University Medical Center Freiburg, München Klinik Schwabing, Evangelisches Krankenhaus Bielefeld, Luzerner Kantonsspital, München Klinik, Institute of Diabetes Research, Technical University of Munich, Hacettepe University, Columbia University, Ludwig-Maximilians-Universität München

OpenAlex ID: A5079853107

Lipopolysaccharide and ceramide docking to CD14 provokes ligand-specific receptor clustering in rafts

2001 · Alexandra Pfeiffer, Alfred Böttcher, et al. · European Journal of Immunology · 401

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The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene

2007 · Klaus Gempel, Haluk Topaloglu, et al. · Brain · 316

Mitochondria and Diabetes: Genetic, Biochemical, and Clinical Implications of the Cellular Energy Circuit

1996 · Klaus-Dieter Gerbitz, Klaus Gempel, et al. · Diabetes · 291

Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients

2007 · Wolfgang Müller-Felber, Rita Horvath, et al. · Neuromuscular Disorders · 245

Hepatocerebral Mitochondrial DNA Depletion Syndrome Caused by Deoxyguanosine Kinase (DGUOK) Mutations

2006 · Peter Freisinger, Nancy Fütterer, et al. · Archives of Neurology · 116

Genetic and structural characterization of the human mitochondrial inner membrane translocase 1 1Edited by J. Karn

1999 · Matthias F. Bauer, Klaus Gempel, et al. · Journal of Molecular Biology · 116

Coenzyme Q10 deficiency and isolated myopathy

2006 · R. Horvath, P. Schneiderat, et al. · Neurology · 114

Adult‐onset glycogen storage disease type 2: clinico‐pathological phenotype revisited

2007 · B. G. H. Schoser, J. Müller‐Höcker, et al. · Neuropathology and Applied Neurobiology · 84

Screening for Carnitine Palmitoyltransferase II Deficiency by Tandem Mass Spectrometry

2002 · K. Gempel, S. Kiechl, et al. · Journal of Inherited Metabolic Disease · 76

Acute Valproate Poisoning

2005 · Florian Eyer, Norbert Felgenhauer, et al. · Journal of Clinical Psychopharmacology · 75

Carnitine Transporter OCTN2 Mutations in Systemic Primary Carnitine Deficiency: A Novel Arg169Gln Mutation and a Recurrent Arg282ter Mutation Associated with an Unconventional Splicing Abnormality

1999 · Barbara Burwinkel, Joachim Kreuder, et al. · Biochemical and Biophysical Research Communications · 69

Rapid Determination of Total Homocysteine in Blood Spots by Liquid Chromatography-Electrospray Ionization-Tandem Mass Spectrometry

2000 · Klaus Gempel, Klaus-Dieter Gerbitz, et al. · Clinical Chemistry · 55

Uptake, clearance and metabolism of TEGDMA in guinea pigs

2002 · Franz-Xaver Reichl, Jürgen Durner, et al. · Dental Materials · 48

Treatment of glycogenosis type V with ketogenic diet

2005 · Verena Busch, Klaus Gempel, et al. · Annals of Neurology · 45

Investigation of citrullinemia type I variants by in vitro expression studies

2008 · Christoph Berning, Iris Bieger, et al. · Human Mutation · 44

Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation

2008 · J. Prestel, K. Gempel, et al. · Journal of Neurology · 35

Mitochondrial Disorders. A Diagnostic Challenge in Clinical Chemistry

1999 · Matthias F. Bauer, Klaus Gempel, et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 24

Monitoring of Ketogenic Diet for Carnitine Metabolites by Subcutaneous Microdialysis

2006 · Alexandra Hack, Verena Busch, et al. · Pediatric Research · 23

"Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old child

2001 · Klaus Gempel, Caroline von Praun, et al. · European Journal of Pediatrics · 19

In-Vitro Carboxymethylation of Low Density Lipoprotein Alters its Metabolism Via the High-Affinity Receptor

1993 · K. Gempel, K. Gerbitz, et al. · Hormone and Metabolic Research · 19

Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry

2001 · S. Stadler, K. Gempel, et al. · Journal of Inherited Metabolic Disease · 17

Biological clearance of HEMA in guinea pigs

2002 · F.X Reichl, J Durner, et al. · Biomaterials · 16

Glykogenose Typ II (M. Pompe)

2005 · L. Burghaus, W. Liu, et al. · Der Nervenarzt · 14

Cystic renal dysplasia as a leading sign of inherited metabolic disease

2007 · Felix Distelmaier, Markus Vogel, et al. · Pediatric Nephrology · 11

Subcutaneous microdialysis for children - safe biochemical tissue monitoring based on a minimal traumatizing no touch insertion technique.

2005 · A Hack, V Busch, et al. · PubMed · 11

Works count: 46

Citation count: 2,323

H-index: 19

I10-index: 27