Dana Novotná

Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects

Jan Lebl, Jan Vosáhlo, Roland Pfaeffle et al. · European Journal of Endocrinology · 2005 · 65 citations

Pendred syndrome among patients with congenital hypothyroidism detected by neonatalscreening: identification of two novel PDS/SLC26A4 mutations

Karolína Banghová, Eva Al Taji, Ondřej Cinek et al. · European Journal of Pediatrics · 2007 · 39 citations

Mendelian Disorder, Genetic Disorder, Inherited Metabolic Disease +5

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

Epidemiology of rare diseases detected by newborn screening in the Czech Republic

Jan David, Petr Chrastina, Karolína Pešková et al. · Central European Journal of Public Health · 2019 · 26 citations · Full text

Secondary pseudohypoaldosteronism in an infant with pyelonephritis.

Zdeněk Doležel, Jiří Štarha, Dana Novotná et al. · PubMed · 2004 · 17 citations