Zita Halasz
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Explore the profile of Zita Halasz including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
113
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Recent Articles
1.
Groeneweg S, van Geest F, Martin M, Dias M, Frazer J, Medina-Gomez C, et al.
Nat Commun
. 2025 Mar;
16(1):2479.
PMID: 40075072
Predicting and quantifying phenotypic consequences of genetic variants in rare disorders is a major challenge, particularly pertinent for 'actionable' genes such as thyroid hormone transporter MCT8 (encoded by the X-linked...
2.
Groeneweg S, van Geest F, Abaci A, Alcantud A, Ambegaonkar G, Armour C, et al.
Lancet Diabetes Endocrinol
. 2020 Jun;
8(7):594-605.
PMID: 32559475
Background: Disordered thyroid hormone transport, due to mutations in the SLC16A2 gene encoding monocarboxylate transporter 8 (MCT8), is characterised by intellectual and motor disability resulting from cerebral hypothyroidism and chronic...
3.
Halasz Z
Orv Hetil
. 2018 Dec;
159(49):2065-2072.
PMID: 30525884
Experimental and clinical data suggest a complex interaction between the endocrine and immune systems. However, only few epidemiological studies are available dealing with endocrine complications in different types of primary...
4.
Bashamboo A, Eozenou C, Jorgensen A, Bignon-Topalovic J, Siffroi J, Hyon C, et al.
Am J Hum Genet
. 2018 Feb;
102(3):487-493.
PMID: 29478779
Emerging evidence from murine studies suggests that mammalian sex determination is the outcome of an imbalance between mutually antagonistic male and female regulatory networks that canalize development down one pathway...
5.
Toke J, Bertalan R, Gergics P, Halasz Z
Orv Hetil
. 2018 Feb;
159(7):278-284.
PMID: 29429351
Developmental disorders affecting the hypothalamic-pituitary system can result in pituitary hormone deficiency showing a diverse clinical presentation. A significant majority of these disorders are closely linked to defects in transcription...
6.
Doleschall M, Torok D, Meszaros K, Luczay A, Halasz Z, Nemeth K, et al.
Orv Hetil
. 2018 Feb;
159(7):269-277.
PMID: 29429350
Congenital adrenal hyperplasia is a group of genetic diseases due to the disablement of 7 genes; one of them is steroid 21-hydroxylase deficiency. The genes of congenital adrenal hyperplasia encode...
7.
David A, Butz H, Halasz Z, Torok D, Nyiro G, Muzsnai A, et al.
Orv Hetil
. 2017 Aug;
158(34):1351-1356.
PMID: 28823207
Introduction: The isolated haploinsufficiency of the SHOX gene is one of the most common cause of short stature determined by monogenic mutations. The heterozygous deviation of the gene can be...
8.
Halasz Z
Orv Hetil
. 2011 Feb;
152(6):221-32.
PMID: 21278027
In this work I analysed the outcome of growth hormone replacement treatment in patients with inherited form of multiple pituitary hormone deficiency and examined diseased-causing mutations of pituitary transcription factor...
9.
Toth B, Wolff A, Halasz Z, Tar A, Szuts P, Ilyes I, et al.
Clin Endocrinol (Oxf)
. 2009 Oct;
72(5):641-7.
PMID: 19863576
Objective: Autoimmune polyendocrine syndrome type I (APS I) is a rare primary immunodeficiency disorder characterized by chronic mucocutaneous candidiasis, multi-organ autoimmunity and ectodermal dysplasia. Autoantibodies to parathyroid and adrenal glands...
10.
Bertalan R, Csabay L, Blazovics A, Rigo Jr J, Varga I, Halasz Z, et al.
Gynecol Endocrinol
. 2007 Sep;
23(10):581-3.
PMID: 17852424
A 33-year-old primagravida with a history of polycystic ovary syndrome was referred because of symptoms of moderate hyperandrogenism. Serum hormone levels, measured regularly from the 7th week of pregnancy until...