Z. Halász

发表

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

E. Husebye, M. Zeher, A. Tar, 2010, Clinical endocrinology.

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

J. Sólyom, G. Fekete, P. Ugocsai, 2010, Journal of endocrinological investigation.

Laterality disturbance and hypopituitarism. A case report of co-existing situs inversus totalis and combined pituitary hormone deficiency

K. Rácz, M. Tóth, E. Gláz, 2008, Journal of endocrinological investigation.

Serum Osteocalcin and Insulin-Like Growth Factor I Levels in Children with Congenital Adrenal Hyperplasia

J. Sólyom, Z. Halász, É. Hosszu, 1999, Hormone Research in Paediatrics.

Mutational Analysis of Hungarian Patients with Androgen Insensitivity Syndrome

K. Rácz, O. Hiort, C. Barta, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

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

K. Rácz, M. Tóth, E. Gláz, 1996, Clinical endocrinology.

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

J. Sólyom, G. Fekete, P. Ugocsai, 2010 .

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

E. Rajpert-De Meyts, K. McElreavey, J. Achermann, 2018, American journal of human genetics.

[The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study].

Anna L. David, A. Patócs, H. Butz, 2017, Orvosi hetilap.

Szteroid-21-hidroxiláz-deficientia, a congenitalis adrenalis hyperplasia leggyakoribb oka

R. Kiss, P. Igaz, M. Tóth, 2018 .

Y-chromosomemarkersinTurnersyndrome: Screeningof130patients

J. Sólyom, G. Fekete, P. Ugocsai, 2010 .

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

T. Battelino, P. Peterson, D. Čiháková, 2001, Human mutation.

Limited value of serum steroid measurements in identification of mild form of 21-hydroxylase deficiency.

M. Garami, J. Sólyom, G. Fekete, 2003, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

[Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].

Z. Halász, 2011, Orvosi hetilap.

High prevalence of PROP1 gene mutations in hungarian patients with childhood-onset combined anterior pituitary hormone deficiency

K. Rácz, L. Kovács, Z. Tömböl, 2006, Endocrine.

Ring Chromosome 18: Clinical, Cytogenetic and Molecular Genetic Studies on Four Patients

T. Eggermann, G. Fekete, Z. Halász, 2004 .

Maternal hyperandrogenism beginning from early pregnancy and progressing until delivery does not produce virilization of a female newborn

K. Rácz, A. Blázovics, Z. Halász, 2007, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

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

E. Bertini, N. Brunetti‐Pierri, M. Polak, 2020, The lancet. Diabetes & endocrinology.