Zita Halász

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

Stefan Groeneweg, Ferdy S. van Geest, Ayhan Abacı et al. · The Lancet Diabetes & Endocrinology · 2020 · 107 citations

Disease Characteristics, Disease Mechanism, Genetic Disorder +10

Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children

Anu Bashamboo, Caroline Eozénou, Anne Jørgensen et al. · The American Journal of Human Genetics · 2018 · 100 citations · Full text

Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED

Daniela Čiháková, Katarina Trebusak, Maarit Heino et al. · Human Mutation · 2001 · 92 citations

Y-chromosome markers in Turner syndrome: Screening of 130 patients

Ágnes Sallai, J. Sólyom, M. Dobos et al. · Journal of Endocrinological Investigation · 2009 · 50 citations

Down Syndrome, Cytogenetics, Genetic Disorder +5

Novel sequence variation of <i>AIRE</i> and detection of interferon‐ω antibodies in early infancy

Beáta Tóth, Anette S. B. Wolff, Zita Halász et al. · Clinical Endocrinology · 2009 · 44 citations