Search Results - "OLAH, Eva"
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Effect of frequently used chemotherapeutic drugs on the cytotoxic activity of human natural killer cells
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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Pharmacometric Analysis of Intranasal and Intravenous Nalbuphine to Optimize Pain Management in Infants
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
Particle physics education in Hungary
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
Endocrine and anatomical findings in a case of Solitary Median Maxillary Central Incisor Syndrome
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
Cytotoxic drug sensitivity of Epstein-Barr virus transformed lymphoblastoid B-cells
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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Pharmacokinetics and tolerability of intranasal or intravenous administration of nalbuphine in infants
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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Association between the Epstein-Barr virus and Hodgkin's lymphoma in the North-Eastern part of Hungary: effects on therapy and survival
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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Clinical and genetic characteristics of craniosynostosis
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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Results of clinical and genetic diagnosis of rare diseases in the Eastern region of Hungary (2007-2013)
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
High‐throughput live‐cell imaging reveals differential inhibition of tumor cell proliferation by human fibroblasts
Published in International journal of cancer (15-06-2011)“…Increasing evidence indicates that cancer development requires changes both in the precancerous cells and in their microenvironment. To study one aspect of the…”
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Variable expressivity of pfeiffer syndrome in a family with FGFR1 p.Pro252Arg mutation
Published in American journal of medical genetics. Part A (01-12-2014)“…Pfeiffer syndrome is an autosomal dominant disorder classically characterized by craniosynostosis, facial dysmorphism and limb anomalies. The majority of cases…”
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De novo mutations of the gene encoding the histone acetyltransferase KAT6B in two patients with Say‐Barber/Biesecker/Young‐Simpson syndrome
Published in American journal of medical genetics. Part A (01-04-2013)“…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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The Wilms' tumour 1 gene as a factor in non-syndromic hypospadias: evidence and controversy
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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Ten-year Experiences on Initial Genetic Examination in Childhood Acute Lymphoblastic Leukaemia in Hungary (1993–2002). Technical Approaches and Clinical Implementation
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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Clinical and genetic characteristics of craniosynostosis in Hungary
Published in American journal of medical genetics. Part A (01-12-2015)“…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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Achondroplasia with multiple-suture craniosynostosis: A report of a new case of this rare association
Published in American journal of medical genetics. Part A (01-10-2013)“…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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Effect of Frequently Used Chemotherapeutic Drugs on Cytotoxic Activity of Human Cytotoxic T-lymphocytes
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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FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies
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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Lissencephaly and Band Heterotopia: LIS1, TUBA1A, and DCX Mutations in Hungary
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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Complete recovery from psychosis upon miglustat treatment in a juvenile Niemann–Pick C patient
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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