Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ágota, Muzsnai"'
Autor:
Dorina ANNÁR, Piroska V. FEHÉR, Sára INCE, Anna MADARASI, Ágota MUZSNAI, Anna KÉKESI, Annamária ZSÁKAI
Publikováno v:
Anthropologiai Közlemények. :69-76
The frequency of X chromosome loss in women increases with ageing. Numerous cases have linked the numerical reduction of sex chromosomes to the development of malignant tumours, recurrent miscarriages and Alzheimer’s disease. The main aim of the st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2a7eab60df540b3100e62f55e84d073
https://doi.org/10.20330/anthropkozl.2021.62.69
https://doi.org/10.20330/anthropkozl.2021.62.69
Autor:
Anna Kekesi, Dorina Annár, Piroska Fehér, Annamária Zsákai, Ágota Muzsnai, Irina Kalabiska, Nicholas Mascie-Taylor, Anna Madarasi
Objectives The health status of an individual is determined not only by their genetic background but also by their physical environment, social environment and access and use of the health care system. The Roma are one of the largest ethnic minority
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c299bbf038f347aa9f3c1fdaa06d44a0
Turner-szindrómások morfológiai jellegei, kariotípusa és kezelésük típusa közötti kapcsolat elemzése
Publikováno v:
Anthropologiai Közlemények. :47-54
Turner-syndrome is a genetic disorder that involves X-chromosome, and affects about 2500–3000 newborn girls around the world. The disease is accompanied by numerous clinical and morphological characteristics, therefore it is very important to study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::015806902015f405d2ce374a9034f96c
https://doi.org/10.20330/anthropkozl.2018.59.47
https://doi.org/10.20330/anthropkozl.2018.59.47
Publikováno v:
Gyermekgyógyászat; 2022, Vol. 73 Issue 4, p312-317, 6p
Autor:
Henriett Butz, Gy Fekete, Attila Tar, Ágota Muzsnai, Attila Patócs, Zsuzsanna Szanto, Gábor Nyírő, Andrea Luczay, Rita Bertalan, Ágnes Sallai, Éva Hosszú, Violetta Csákváry, Enikő Felszeghy, Zita Halász, Imre Zoltan Kun, Dóra Török, Anna David
Publikováno v:
Orvosi Hetilap. 158:1351-1356
Abstract: 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 detected in 2–15% of patients with idiopathic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de2355c2ef87c05d412daf7995cac4b5
https://doi.org/10.1556/650.2017.30829
https://doi.org/10.1556/650.2017.30829
Akademický článek
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Publikováno v:
Anthropologiai Közlemények. 56:129-138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a29eb17f08b36b3e1f85b67fa0045782
https://doi.org/10.20330/anthropkozl.2015.56.129
https://doi.org/10.20330/anthropkozl.2015.56.129
Autor:
Anna, Dávid, Henriett, Butz, Zita, Halász, Dóra, Török, Gábor, Nyirő, Ágota, Muzsnai, Violetta, Csákváry, Andrea, Luczay, Ágnes, Sallai, Éva, Hosszú, Enikő, Felszeghy, Attila, Tar, Zsuzsanna, Szántó, Gy László, Fekete, Imre, Kun, Attila, Patócs, Rita, Bertalan
Publikováno v:
Orvosi hetilap. 158(34)
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 detected in 2-15% of patients with idiopathic short stature (ISS), in 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1439382d4249def747ab869847cecaf0
https://pubmed.ncbi.nlm.nih.gov/28823207
https://pubmed.ncbi.nlm.nih.gov/28823207
Autor:
Ágota Muzsnai, Ferenc Péter
Publikováno v:
Pediatric Clinics of North America. 58:1099-1115
This article summarizes the ontogenesis and genetics of the thyroid with regards to its possible congenital dysfunction and briefly refers to the roles of the mother-placenta-fetal unit, iodine effect, and organic and functional changes of the negati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e066d6fa3bd10f70ec72b9a1f3c298d8
https://doi.org/10.1016/j.pcl.2011.07.002
https://doi.org/10.1016/j.pcl.2011.07.002
Publikováno v:
American Journal of Human Biology. :e22966
Objectives The estimation of skeletal maturity is a useful tool in pediatric practice to determine the degree of delay or advancement in growth disorders and the effectiveness of treatment in conditions that influence linear growth. Skeletal maturity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1c87ef4c1aa9aa5734167a30b16c419
https://doi.org/10.1002/ajhb.22966
https://doi.org/10.1002/ajhb.22966