tallózása szerző szerint "Szilágyi Ágnes"

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4G/5G polymorphism of PAI-1 gene is associated with multiple organ dysfunction and septic shock in pneumonia induced severe sepsis: prospective, observational, genetic study

Madách Krisztina; Aladzsity István; Szilágyi Ágnes; Füst György; Gál János; Pénzes István; Prohászka Zoltán (2010)

Introduction: Activation of inflammation and coagulation are closely related and mutually interdependent in sepsis. The acute-phase protein, plasminogen activator inhibitor-1 (PAI-1) is a key element in the inhibition ...
A mannóz-kötő lektin szerepe daganatos gyermekek lázas állapotaiban

Fadgyas Balázs; Papp Éva; Szilágyi Ágnes; Prohászka Zoltán; Müller Brigitta; Csóka, Monika; Kovács, Gábor (2011)
A unique haplotype of RCCX copy number variation

Doleschall Márton; Luczay Andrea; Koncz Klára; Hadzsiev Kinga; Erhardt Éva; Szilágyi Ágnes; Doleschall Zoltán; Németh Krisztina; Török Dóra; Prohászka Zoltán; Gereben Balázs; Fekete György; Gláz Edit; Igaz Péter; Korbonits Márta; Tóth Miklós; Rácz Károly; Patócs Attila (2017)

There is a difficulty in the molecular diagnosis of congenital adrenal hyperplasia (CAH) due to the c.955C>T (p.(Q319*), formerly Q318X, rs7755898) variant of the CYP21A2 gene. Therefore, a systematic assessment of the ...
Common Genetic Variants of the Human Steroid 21-Hydroxylase Gene (CYP21A2) Are Related to Differences in Circulating Hormone Levels.

Doleschall Márton; Szabo JA; Pazmandi J; Szilágyi Ágnes; Koncz Klára; Farkas Henriette; Tóth Miklós; Igaz Péter; Gláz Edit; Prohászka Zoltán; Korbonits M; Rácz Károly; Füst György; Patócs Attila Balázs (2014)

PURPOSE: Systematic evaluation of the potential relationship between the common genetic variants of CYP21A2 and hormone levels. METHODS: The relationships of CYP21A2 intron 2 polymorphisms and haplotypes with diverse ...
Comparative analysis of IL6 and IL6 receptor gene polymorphisms in mastocytosis

Rausz Eszter Zsófia; Szilágyi Ágnes; Nedoszytko B; Lange M; Niedoszytko M; Lautner-Csorba Orsolya; Falus András; Aladzsity István; Kokai Márta; Valent P; Marschalkó Márta; Hidvégi Bernadett; Szakonyi József; Csomor Judit; Várkonyi Judit (2013)

Mastocytosis is a rare disease with reported high interleukin-6 (IL6) levels influencing disease severity. The present study investigated polymorphisms within the genes that encode IL6 and its receptor (IL6R) in relation ...
Efficacy of eculizumab in a patient with immunoadsorption- dependent catastrophic antiphospholipid syndrome: A case report

Kronbichler, Andreas; Frank, Renate; Kirschfink, Michael; Szilágyi Ágnes; Csuka Dorottya; Prohászka, Zoltán; Schratzberger, Peter; Lhotta, Karl; Mayer, Gert (2014)

Catastrophic antiphospholipid syndrome (CAPS) is a rare but devastating complication in patients with antiphospholipid syndrome (APS) with a high morbidity and mortality. We describe a case of a 30-year old female patient ...
Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene

Bánlaki Zsófia; Szabo JA; Szilágyi Ágnes; Patócs Attila Balázs; Prohászka Zoltán; Füst György; Doleschall Márton (2013)

The RCCX region is a complex, multiallelic, tandem copy number variation (CNV). Two complete genes, complement component 4 (C4) and steroid 21-hydroxylase (CYP21A2, formerly CYP21B), reside in its variable region. RCCX is ...

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tallózása szerző szerint "Szilágyi Ágnes"

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