Search Results - "OLAH, Eva"

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  1. 1

    Effect of frequently used chemotherapeutic drugs on the cytotoxic activity of human natural killer cells by Markasz, Laszlo, Stuber, Gyorgy, Vanherberghen, Bruno, Flaberg, Emilie, Olah, Eva, Carbone, Ennio, Eksborg, Staffan, Klein, Eva, Skribek, Henriette, Szekely, Laszlo

    Published in Molecular cancer therapeutics (01-02-2007)
    “…Tumors are considered to be possible targets of immunotherapy using stimulated and expanded autologous or allogeneic natural killer (NK) cells mismatched for…”
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  2. 2

    Pharmacometric Analysis of Intranasal and Intravenous Nalbuphine to Optimize Pain Management in Infants by Pfiffner, Miriam, Berger-Olah, Eva, Vonbach, Priska, Pfister, Marc, Gotta, Verena

    Published in Frontiers in pediatrics (02-03-2022)
    “…The objective of this pharmacometric (PMX) study was to (i) characterize population pharmacokinetics (PPK) and exposure-pain response associations following…”
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  3. 3

    Particle physics education in Hungary by Oláh, Éva, Ádám, Péter, Béni, Noémi, Hamar, Gergö, Horváth, Árpád, Horváth, Dezsö, Jancsó, Gábor, Jarosievitz, Beáta, Lévai, Péter, Péntek, Csilla, Sükösd, Csaba, Szillási, Zoltán, Trócsányi, Zoltán, Újvári, Balázs, Vámi, Tamás, Varga, Dezsö

    Published in Nuclear and particle physics proceedings (01-04-2016)
    “…In recent years various educational activities have been pursued in Hungary with the aim to raise the interest of high school students in natural sciences, and…”
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  4. 4

    Endocrine and anatomical findings in a case of Solitary Median Maxillary Central Incisor Syndrome by Szakszon, Katalin, Felszeghy, Enikő, Csízy, István, Józsa, Tamás, Káposzta, Rita, Balogh, Erzsébet, Oláh, Éva, Balogh, István, Berényi, Ervin, Knegt, Alida C, Ilyés, István

    Published in European journal of medical genetics (01-02-2012)
    “…Abstract Solitary Median Maxillary Central Incisor Syndrome (SMMCI) is a rare malformation syndrome consisting of multiple, mainly midline defects. Some…”
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  5. 5

    Cytotoxic drug sensitivity of Epstein-Barr virus transformed lymphoblastoid B-cells by Markasz, Laszlo, Stuber, György, Flaberg, Emilie, Jernberg, Asa Gustafsson, Eksborg, Staffan, Olah, Eva, Skribek, Henriette, Szekely, Laszlo

    Published in BMC cancer (13-11-2006)
    “…Epstein-Barr virus (EBV) is the causative agent of immunosuppression associated lymphoproliferations such as post-transplant lymphoproliferative disorder…”
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  6. 6

    Pharmacokinetics and tolerability of intranasal or intravenous administration of nalbuphine in infants by Pfiffner, Miriam, Gotta, Verena, Pfister, Marc, Vonbach, Priska, Berger-Olah, Eva

    Published in Archives of disease in childhood (01-01-2023)
    “…ObjectivesIntranasal nalbuphine could be a safe, efficacious and non-invasive alternative to parenteral pain medication in infants. We aimed to assess…”
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  7. 7

    Association between the Epstein-Barr virus and Hodgkin's lymphoma in the North-Eastern part of Hungary: effects on therapy and survival by Keresztes, Katalin, Miltenyi, Zsofia, Bessenyei, Beata, Beck, Zoltan, Szollosi, Zoltan, Nemes, Zoltan, Olah, Eva, Illes, Arpad

    Published in Acta haematologica (01-01-2006)
    “…This retrospective study included 109 patients with Hodgkin's lymphoma (HL; 45 females, 64 males). In 47 of the 109 HL patients (43%), immunohistochemical…”
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  8. 8

    Clinical and genetic characteristics of craniosynostosis by Bessenyei, Beáta, Oláh, Eva

    Published in Orvosi hetilap (02-03-2014)
    “…Craniosynostosis is caused by premature fusion of one or more cranial sutures leading to deformity of the cranium. Depending on the type and number of the…”
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  9. 9

    Results of clinical and genetic diagnosis of rare diseases in the Eastern region of Hungary (2007-2013) by Szakszon, Katalin, Balogh, Erzsébet, Ujfalusi, Anikó, Bessenyei, Beáta, P Szabó, Gabriella, Balogh, István, Oláh, Eva

    Published in Orvosi hetilap (02-03-2014)
    “…80% of rare diseases have a genetic origin, and 50% manifest themselves as congenital anomalies. Their adequate health care includes early recognition of…”
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  10. 10
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    Variable expressivity of pfeiffer syndrome in a family with FGFR1 p.Pro252Arg mutation by Bessenyei, Beáta, Tihanyi, Mariann, Hartwig, Marianna, Szakszon, Katalin, Oláh, Éva

    “…Pfeiffer syndrome is an autosomal dominant disorder classically characterized by craniosynostosis, facial dysmorphism and limb anomalies. The majority of cases…”
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  12. 12

    De novo mutations of the gene encoding the histone acetyltransferase KAT6B in two patients with Say‐Barber/Biesecker/Young‐Simpson syndrome by Szakszon, Katalin, Salpietro, Carmelo, Kakar, Naseebullah, Knegt, Alida C., Oláh, Éva, Dallapiccola, Bruno, Borck, Guntram

    “…The Say‐Barber/Biesecker/Young‐Simpson (SBBYS) type of the blepharophimosis–mental retardation syndrome group (Ohdo‐like syndromes) is a multiple congenital…”
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  13. 13

    The Wilms' tumour 1 gene as a factor in non-syndromic hypospadias: evidence and controversy by Buglyó, Gergely, Beyer, Dániel, Biró, Sándor, Oláh, Éva

    Published in Pathology (01-06-2018)
    “…Hypospadias is one of the most frequent congenital anomalies of the male external genitalia. Its pathogenesis is due to largely unknown or poorly understood…”
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  14. 14

    Ten-year Experiences on Initial Genetic Examination in Childhood Acute Lymphoblastic Leukaemia in Hungary (1993–2002). Technical Approaches and Clinical Implementation by Olah, Eva, Balogh, Erzsebet, Pajor, Laszlo, Jakab, Zsuzsanna

    Published in Pathology oncology research (01-03-2011)
    “…A nationwide study was started in 1993 to provide genetic diagnosis for all newly diagnosed childhood ALL cases in Hungary using cytogenetic examination,…”
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  15. 15

    Clinical and genetic characteristics of craniosynostosis in Hungary by Bessenyei, Beáta, Nagy, Andrea, Szakszon, Katalin, Mokánszki, Attila, Balogh, Erzsébet, Ujfalusi, Anikó, Tihanyi, Mariann, Novák, László, Bognár, László, Oláh, Éva

    “…Craniosynostosis, the premature closure of cranial sutures, is a common craniofacial disorder with heterogeneous etiology and appearance. The purpose of this…”
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  16. 16

    Achondroplasia with multiple-suture craniosynostosis: A report of a new case of this rare association by Bessenyei, Beáta, Nagy, Andrea, Balogh, Erzsébet, Novák, László, Bognár, László, Knegt, Alida C., Oláh, Éva

    “…We report on a female patient with an exceedingly rare combination of achondroplasia and multiple‐suture craniosynostosis. Besides the specific features of…”
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  17. 17

    Effect of Frequently Used Chemotherapeutic Drugs on Cytotoxic Activity of Human Cytotoxic T-lymphocytes by MARKASZ, Laszlo, SKRIBEK, Henriette, UHLIN, Michael, OTVOS, Rita, FLABERG, Emilie, EKSBORG, Staffan, OLAH, Eva, STUBER, Gyorgy, SZEKELY, Laszlo

    Published in Journal of immunotherapy (1997) (01-04-2008)
    “…Tumors are considered to be possible targets of immunotherapy using stimulated and expanded cytotoxic T-lymphocytes (CTL). It is important to consider the…”
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  18. 18

    FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies by Madar, László, Szakszon, Katalin, Pfliegler, György, Szabó, Gabriella P., Brúgós, Boglárka, Ronen, Natali, Papp, Judit, Zahuczky, Katalin, Szakos, Erzsébet, Fekete, György, Oláh, Éva, Koczok, Katalin, Balogh, István

    Published in Journal of biotechnology (10-08-2019)
    “…•FBN1 gene testing in individuals with Marfan syndrome and other fibrillinopathies.•Identification of novel and recurrent causal and potentially causal FBN1…”
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  19. 19

    Lissencephaly and Band Heterotopia: LIS1, TUBA1A, and DCX Mutations in Hungary by Mokánszki, Attila, Körhegyi, Ivett, Szabó, Nóra, Bereg, Edit, Gergev, Gyurgyinka, Balogh, Erzsébet, Bessenyei, Beáta, Sümegi, Andrea, Morris-Rosendahl, Deborah J., Sztriha, László, Oláh, Éva

    Published in Journal of child neurology (01-12-2012)
    “…The spectrum of lissencephaly ranges from absent (agyria) or decreased (pachygyria) convolutions to less severe malformation known as subcortical band…”
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  20. 20

    Complete recovery from psychosis upon miglustat treatment in a juvenile Niemann–Pick C patient by Szakszon, Katalin, Szegedi, István, Magyar, Ágnes, Oláh, Éva, Andrejkovics, Mónika, Balla, Petra, Lengyel, András, Berényi, Ervin, Balogh, István

    Published in European journal of paediatric neurology (01-01-2014)
    “…Abstract Niemann–Pick disease type C is a rare lipid trafficking disorder characterized by the accumulation of cholesterol and glycosphingolipids in the brain…”
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