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Endocrine complications in primary immunodeficiency diseases

Orvosi hetilap, 2018-12, Vol.159 (49), p.2065

Halász, Zita

2018

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

American journal of human genetics, 2018-03, Vol.102 (3), p.487-493

2018

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

Clinical endocrinology (Oxford), 2010-05, Vol.72 (5), p.641-647

2010

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

Endocrine, 2006-12, Vol.30 (3), p.255-260

2006

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

Orvosi hetilap, 2011-02, Vol.152 (6), p.221

Halász, Zita

2011

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

Orvosi hetilap, 2017-08, Vol.158 (34), p.1351

2017

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

Human mutation, 2001-09, Vol.18 (3), p.225-232

2001

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

Journal of endocrinological investigation, 2008, Vol.31 (1), p.74-78

2008

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Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED: AIRE Mutations in CEE APECED Patients

Human mutation, 2001-09, Vol.18 (3), p.225-232

2001

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Novel sequence variation of AIRE and detection of interferon-[omega] antibodies in early infancy

Clinical endocrinology (Oxford), 2010-05, Vol.72 (5), p.641

2010

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

Clinical endocrinology (Oxford), 2010-05, Vol.72 (5), p.641-647

2010

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Mutational analysis of Hungarian patients with androgen insensitivity syndrome

Journal of pediatric endocrinology & metabolism : JPEM, 2003-03, Vol.16 (3), p.367

2003

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

International journal of human genetics, 2004-09, Vol.4 (3), p.197-200

2004

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

Gynecological endocrinology, 2007-10, Vol.23 (10), p.581-583

2007

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

Clinical endocrinology (Oxford), 1996-09, Vol.45 (3), p.369-370

1996

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Two Families With Hereditary Diabetes Insipidus Not Due to Osmoreceptor Failure

Hormone and metabolic research, 1992-02, Vol.24 (2), p.70-72

1992

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Postoperative interictal spikes during sleep contralateral to the operated side is associated with unfavourable surgical outcome in patients with preoperative bitemporal spikes

Seizure (London, England), 2004-10, Vol.13 (7), p.460-466

2004

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Endocrine complications in primary immunodeficiency diseases

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

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

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

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

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

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

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

Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED: AIRE Mutations in CEE APECED Patients

Novel sequence variation of AIRE and detection of interferon-[omega] antibodies in early infancy

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

Mutational analysis of Hungarian patients with androgen insensitivity syndrome

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

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

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

Two Families With Hereditary Diabetes Insipidus Not Due to Osmoreceptor Failure

Postoperative interictal spikes during sleep contralateral to the operated side is associated with unfavourable surgical outcome in patients with preoperative bitemporal spikes

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