Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Zoltán Prohászka"'
Autor:
Gabor G. Kovacs, Ágnes Szilágyi, Marianna Dobi, Dorottya Csuka, Ferenc Fekete, Lilian Varga, Csaba Bereczki, Zoltán Prohászka
Publikováno v:
The Pediatric infectious disease journal. 40(2)
The complement system is essential for protection against infections in oncologic patients because of the chemotherapy-induced immunosuppression. One of the key elements in the activation of the complement system via the lectin pathway is the appropr
Autor:
Dóra Inotai, György Sinkovits, Anikó Szilvási, Ágnes Szilágyi, Marienn Réti, Attila Tordai, Katalin Rázsó, Zoltán Prohászka, Péter Farkas
Publikováno v:
Human Immunology. 78:80-87
The acquired form of idiopathic thrombotic thrombocytopenic purpura (TTP) is an autoimmune disease, in which the underlying ADAMTS13-deficiency is caused by inhibitory autoantibodies against the protease. Human leukocyte antigens (HLA), responsible f
Autor:
Zoltán Prohászka, László Wagner, Attila Szabo, Kata Kelen, Beáta Takács, Klaus Arbeiter, Ágnes Haris, Dorottya Csuka, Ágnes Szilágyi, György Reusz, Marienn Réti, Thomas Müller, B. Paul Morgan, Krisztina Rusai, Nóra Szarvas, Szilárd Török
Publikováno v:
Molecular Immunology. 71:10-22
Atypical hemolytic uremic syndrome (aHUS) is a rare disorder caused by dysregulation of the complement alternative pathway, and associated with mutations in genes of complement components and regulators. In the recent years several studies have been
Publikováno v:
Molecular immunology. 89
Hereditary angioedema (HAE) is a rare, but potentially life-threatening disorder, characterized by acute, recurring, and self-limiting edematous episodes of the face, extremities, trunk, genitals, upper airways, or the gastrointestinal tract. HAE may
Autor:
Tamás Tirczka, Ákos Tóth, Brigitta Berta, Csilla Jekkel, Zoltán Prohászka, Zsófia Bognár, Anita Ábrahám, Tímea Erdősi
Publikováno v:
Acta microbiologica et immunologica Hungarica. 64(1)
A Hungarian soldier previously immunized against Neisseria meningitidis by quadrivalent polysaccharide vaccine was twice infected with meningococci within six weeks. The patient was treated with ceftriaxone during both episodes and he successfully re
Autor:
Gábor Széplaki, Peter Garred, Kristóf Hirschberg, Edit Dósa, István Karádi, György Acsády, László Entz, Lilian Varga, Tímea Gombos, George Füst, Zoltán Prohászka
Publikováno v:
Molecular Immunology. 45:3289-3294
Complement activation plays an important role in ischemia/reperfusion (I/R) injury. The objective of the present study was to detect the presence and mechanism of complement activation in patients who underwent carotid endarterectomy (CEA).Complement
Autor:
Sigurdur Boðvarsson, Maria Sasvari-Szekely, Zsolt Ronai, G.J. Arason, George Füst, Perla Thorbjornsdottir, Ragnhildur Kolka, Zoltán Prohászka, Sigurður Thór Sigurðarson, G. Thorgeirsson, Margit Kovács, Garðar Sigurðsson, Bernadett Blaskó
Publikováno v:
International Immunology. 20:31-37
Background and Objectives: Some recent data indicate that risk of death after acute coronary syndrome is under genetic control. Previously, we found that the C4B*Q0 genotype (low copy number of the C4B gene that encodes the fourth component of comple
Autor:
Edit Dósa, Szabolcs Rugonfalvi-Kiss, Judit Laki, Peter Garred, László Romics, Attila Szabo, György Acsádi, László Selmeci, László Entz, Márta Kókai, George Füst, Hans O. Madsen, István Karádi, László Cervenak, Zoltán Prohászka
Publikováno v:
Stroke. 38:2247-2253
Background and Purpose—Recently we found that the incidence of restenosis after carotid endarterectomy was significantly higher in patients homozygous for the normal genotype of mannose-binding lectin (MBL2) than in with patients withMBL2variant ge
Autor:
Zoltán Széplaki, Zoltán Prohászka, Ádám Fazakas, Gábor Széplaki, Margit Kovács, George Füst, Attila Molvarec, István Karádi
Publikováno v:
Clinica Chimica Acta. 382:100-105
Background Ischemic stroke is a multifactorial disorder with genetic and environmental components. The aim of our study was to investigate whether two polymorphisms of the estrogen receptor α (ESR1) gene (ESR1 c.454-397T>C and c.454-351A>G) are asso
Publikováno v:
Human Heredity. 62:77-83
Aims: Previously we reported an association between levels of anti-Hsp60 autoantibodies and interleukin-6 (IL-6) –174 SNP in Finnish population. The aim of this study was to investigate the same association in an independent population and to study