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Otto Mehls

Researcher at Heidelberg University

Publications -  201
Citations -  10322

Otto Mehls is an academic researcher from Heidelberg University. The author has contributed to research in topics: Kidney disease & Renal function. The author has an hindex of 54, co-authored 200 publications receiving 9764 citations. Previous affiliations of Otto Mehls include Boston Children's Hospital & University of Cologne.

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Advanced Coronary and Carotid Arteriopathy in Young Adults With Childhood-Onset Chronic Renal Failure

TL;DR: Young adults with childhood-onset CRF have a high prevalence of arteriopathy associated with indicators of microinflammation, hyperparathyroidism, calcium-phosphate overload, and hyperhomocysteinemia but not traditional atherogenic risk factors.
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Normative values for intima-media thickness and distensibility of large arteries in healthy adolescents.

TL;DR: Morphological and functional measures of large arteries should be normalized to take account of changes during adolescence and skewed distributions, as relative body mass, systolic blood pressure and/or pulse pressure are determinants of IMT and elasticity.
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Prevalence of Mutations in Renal Developmental Genes in Children with Renal Hypodysplasia: Results of the ESCAPE Study

TL;DR: Gene mutations that have dominant inheritance and cause RHD, urinary tract anomalies, and defined extrarenal symptoms have been identified in TCF2, PAX2, EYA1, SIX1, and SALL1; it is interesting that a Six1 sequence variant was identified in two siblings with renal-coloboma syndrome as a result of a PAX2 mutation, suggesting an oligogenic inheritance.
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The Pharmacokinetic-Pharmacodynamic Relationship for Total and Free Mycophenolic Acid in Pediatric Renal Transplant Recipients: A Report of the German Study Group on Mycophenolate Mofetil Therapy

TL;DR: Investigation of the pharmacokinetic (PK)/pharmacodynamic relationship of total and free MPA and PK values for the assessment of an individual's MPA PK parameters indicates that therapeutic drug monitoring of MPA has the potential for optimization of MMF efficacy in this patient population by steering patients away from the low values of M PA PK variables that are associated with an increased rejection risk.