D. Zemková

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe

Thilo Dörk, Milan Maçek, Frauke Mekus et al. · Human Genetics · 2000 · 145 citations

Fibrosis, Mendelian Disorder, Genetic Disorder +11

Cholelithiasis and choledocholithiasis in children; risk factors for development

Barbora Frýbová, Jindra Lochmannová, Ladislav Douda et al. · PLoS ONE · 2018 · 83 citations · Full text

Low-dose insulin therapy in patients with cystic fibrosis and early-stage insulinopenia prevents deterioration of lung function: a 3-year prospective study

Stanislava Koloušková, D. Zemková, Jana Bartošová et al. · Journal of Pediatric Endocrinology and Metabolism · 2011 · 51 citations

Distribution of human β-defensin polymorphisms in various control and cystic fibrosis populations

Anne Vankeerberghen, Olga Scudiero, K. De Boeck et al. · Genomics · 2005 · 37 citations

Genetics, Pathogenesis, Genetic Epidemiology +7

Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius

Ondřej Souček, Jiřina Zapletalová, D. Zemková et al. · The Journal of Clinical Endocrinology & Metabolism · 2013 · 36 citations · Full text