Gunter Ŝimić-Schleicher

Evidence for Genetic Heterogeneity of Pseudohypoaldosteronism Type 1: Identification of a Novel Mutation in the Human Mineralocorticoid Receptor in one Sporadic Case and No Mutations in Two Autosomal Dominant Kindreds

Matthias Viemann, Michael Peter, Juan Pedro López-Siguero et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 62 citations

Mendelian Disorder, Family Members, Sodium Homeostasis +15

Prevalence of prediabetes and type 2 diabetes in children with obesity and increased transaminases in European German‐speaking countries. Analysis of the APV initiative

Florian Koutny, Daniel Weghuber, Esther Bollow et al. · Pediatric Obesity · 2019 · 48 citations · Full text

BMI or BIA: Is Body Mass Index or Body Fat Mass a Better Predictor of Cardiovascular Risk in Overweight or Obese Children and Adolescents?

Barbara Bohn, Manfred J. Müller, Gunter Ŝimić-Schleicher et al. · Obesity Facts · 2015 · 40 citations · Full text

Carboxyl-Terminal Mutations in 3β-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia

Maik Welzel, Nele Wüstemann, Gunter Ŝimić-Schleicher et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 35 citations · Full text

News on Clinical Details and Treatment in PGM1-CDG

Esther Schrapers, Laura C. Tegtmeyer, Gunter Ŝimić-Schleicher et al. · JIMD Reports · 2015 · 21 citations · Full text