Zdeněk Doležel

Intravitreal pegaptanib combined with diode laser therapy for stage 3+ retinopathy of prematurity in zone I and posterior zone II

Rudolf Autrata, Inka Krejčířová, Kateřina Šenková et al. · European Journal of Ophthalmology · 2012 · 94 citations

Modern diagnostic approach to hereditary xanthinuria

Martin Mraz, Olha Hurba, Josef Bártl et al. · Urolithiasis · 2014 · 51 citations

Urology, Mendelian Disorder, Genetic Disorder +5

Compound Heterozygous Mutations in the Vitamin D Receptor in a Patient With Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets With Alopecia

Yulin Zhou, Jining Wang, Peter J. Malloy et al. · Journal of Bone and Mineral Research · 2008 · 34 citations · Full text

Mutant Vdr, Mendelian Disorder, Genetic Disorder +11

[Effects of intravitreal pegaptanib or bevacizumab and laser in treatment of threshold retinopathy of prematurity in zone I and posterior zone II--four years results].

Rudolf Autrata, Kateřina Šenková, Marie Holoušová et al. · PubMed · 2012 · 23 citations

Controlled Diet in Phenylketonuria and Hyperphenylalaninemia may Cause Serum Selenium Deficiency in Adult Patients: The Czech Experience

Dagmar Procházková, Jiří Jarkovský, Hana Vinohradská et al. · Biological Trace Element Research · 2013 · 22 citations

Nutrition, Serum Selenium Deficiency, Urology +8