Showing results (1-10 of 13) with videos related to
Sort By:
Pageof 2
Orvosi Hetilap|February 1, 2011
[Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary]Zita HalászOrvosi Hetilap|December 12, 2018
[Endocrine complications in primary immunodeficiency diseases]Zita HalászOrvosi Hetilap|February 13, 2018
[Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency]Judit Tőke, Rita Bertalan, Péter Gergics, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 23, 2003
Mutational analysis of Hungarian patients with androgen insensitivity syndromeDóra Scheiber, Csaba Barta, Zita Halász, et al.Endocrine|May 29, 2007
High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiencyZita Halász, Judit Toke, Attila Patócs, et al.Clinical Endocrinology|October 30, 2009
Novel sequence variation of AIRE and detection of interferon-omega antibodies in early infancyBeáta Tóth, Anette S B Wolff, Zita Halász, et al.Orvosi Hetilap|February 13, 2018
[Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia]Márton Doleschall, Dóra Török, Katalin Mészáros, et al.Orvosi Hetilap|August 22, 2017
[The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study]Anna Dávid, Henriett Butz, Zita Halász, et al.American Journal of Human Genetics|February 27, 2018
Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX ChildrenAnu Bashamboo, Caroline Eozenou, Anne Jorgensen, et al.International Journal of Neonatal Screening|November 24, 2025
Celebrating 50 Years of Nationwide Newborn Screening in Hungary-Review, Current Situation, and Future DirectionsPéter Monostori, Ildikó Szatmári, Ákos Baráth, et al.Pageof 2