Works matching AU Zita, Halász

Results: 11

Mutational Analysis of Hungarian Patients with Androgen Insensitivity Syndrome.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2003, v. 16, n. 3, p. 367, doi. 10.1515/jpem.2003.16.3.367

By:

Scheiber, Dora;
Barta, Csaba;
Halász, Zita;
Sallai, Agnes;
Rácz, Károly;
Ságodi, László;
Fekete, Gyórgy;
Hiort, Olaf;
Solyom, János

Publication type:

Article

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

Published in:

Human Mutation, 2001, v. 18, n. 3, p. 225, doi. 10.1002/humu.1178

By:

Cihakova, Daniela;
Trebusak, Katarina;
Heino, Maarit;
Fadeyev, Valentin;
Tiulpakov, Anatoly;
Battelino, Tadej;
Tar, Attila;
Halász, Zita;
Blümel, Peter;
Tawfik, Sameh;
Krohn, Kai;
Lebl, Jan;
Peterson, Pärt

Publication type:

Article

In memoriam Prof. Dr. Sólyom János (1939-2024).

Published in:

Gyermekgyógyászat, 2024, v. 75, n. 2, p. 75

By:

Andrea, Luczay;
Zita, Halász

Publication type:

Article

Fókuszban az achondroplasia.

Published in:

Gyermekgyógyászat, 2022, v. 73, n. 4, p. 274

By:

Zita, Halász

Publication type:

Article

Kedves Kolléga! Kedves Olvasó!

Published in:

Gyermekgyógyászat, 2022, v. 73, n. 4, p. 255

By:

Éva, Erhardt;
Zita, Halász

Publication type:

Article

Novel sequence variation of AIRE and detection of interferon-ω antibodies in early infancy.

Published in:

Clinical Endocrinology, 2010, v. 72, n. 5, p. 641, doi. 10.1111/j.1365-2265.2009.03740.x

By:

Tóth, Beáta;
Wolff, Anette S. B.;
Halász, Zita;
Tar, Attila;
Szüts, Péter;
Ilyés, István;
Erdős, Melinda;
Szegedi, Gyula;
Husebye, Eystein S.;
Zeher, Margit;
Maródi, Lászl

Publication type:

Article

Adrenal tumour associated with silent 21-hydroxylase deficiency in a male or with a classic form of 21-hydroxylase defect in a female?

Published in:

Clinical Endocrinology, 1996, v. 45, n. 3, p. 369, doi. 10.1046/j.1365-2265.1996.00818.x

By:

Tóth, Miklós;
Rácz, Károly;
Halász, Zita;
Gláz, Edit

Publication type:

Article

Endokrin szövődmények primer immundeficientiában.

Published in:

Hungarian Medical Journal / Orvosi Hetilap, 2018, v. 159, n. 49, p. 2065, doi. 10.1556/650.2018.31122

By:

Halász, Zita

Publication type:

Article

Genetikai tényezők a hypopituitarismus kialakulásában. A transzkripciós faktorok szerepe az agyalapimirigy-elégtelenség hátterében: Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency

Published in:

Hungarian Medical Journal / Orvosi Hetilap, 2018, v. 159, n. 7, p. 278, doi. 10.1556/650.2018.31029

By:

Tőke, Judit;
Bertalan, Rita;
Gergics, Péter;
Halász, Zita

Publication type:

Article

Szteroid-21-hidroxiláz-deficientia, a congenitalis adrenalis hyperplasia leggyakoribb oka: Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia.

Published in:

Hungarian Medical Journal / Orvosi Hetilap, 2018, v. 159, n. 7, p. 269, doi. 10.1556/650.2018.30986

By:

Doleschall, Márton;
Török, Dóra;
Mészáros, Katalin;
Luczay, Andrea;
Halász, Zita;
Németh, Krisztina;
Szücs, Nikolette;
Kiss, Róbert;
Tőke, Judit;
Sólyom, János;
Fekete, György;
Patócs, Attila;
Igaz, Péter;
Tóth, Miklós

Publication type:

Article

A SHOX géndeletio előfordulása idiopáthiás alacsonynövésben. Multicentrikus tanulmány: The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study.

Published in:

Hungarian Medical Journal / Orvosi Hetilap, 2017, v. 158, n. 34, p. 1351, doi. 10.1556/650.2017.30829

By:

Dávid, Anna;
Butz, Henriett;
Halász, Zita;
Török, Dóra;
Nyirő, Gábor;
Muzsnai, Ágota;
Csákváry, Violetta;
Luczay, Andrea;
Sallai, Ágnes;
Hosszú, Éva;
Felszeghy, Enikő;
Tar, Attila;
Szántó, Zsuzsanna;
Fekete, Gy. László;
Kun, Imre;
Patócs, Attila;
Bertalan, Rita

Publication type:

Article