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Variable expressivity of pfeiffer syndrome in a family with FGFR1 p.Pro252Arg mutation

American journal of medical genetics. Part A, 2014-12, Vol.164A (12), p.3176-3179

2014

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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

American journal of medical genetics. Part A, 2013-04, Vol.161 (4), p.884-888

2013

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Achondroplasia with multiple-suture craniosynostosis: A report of a new case of this rare association

American journal of medical genetics. Part A, 2013-10, Vol.161A (10), p.2641-2644

2013

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Clinical and genetic characteristics of craniosynostosis in Hungary

American journal of medical genetics. Part A, 2015-12, Vol.167A (12), p.2985-2991

2015

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The Wilms' tumour 1 gene as a factor in non-syndromic hypospadias: evidence and controversy

Pathology, 2018-06, Vol.50 (4), p.377-381

2018

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Effect of frequently used chemotherapeutic drugs on the cytotoxic activity of human natural killer cells

Molecular cancer therapeutics, 2007-02, Vol.6 (2), p.644-654

2007

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FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies

Journal of biotechnology, 2019-08, Vol.301, p.105-111

2019

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Lissencephaly and Band Heterotopia: LIS1, TUBA1A, and DCX Mutations in Hungary

Journal of child neurology, 2012-12, Vol.27 (12), p.1534-1540

2012

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Complete recovery from psychosis upon miglustat treatment in a juvenile Niemann–Pick C patient

European journal of paediatric neurology, 2014-01, Vol.18 (1), p.75-78

2014

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A patient with Smith–Lemli–Opitz syndrome: novel mutation of the DHCR7 gene and effects of therapy with simvastatin and cholesterol supplement

European journal of pediatrics, 2010, Vol.169 (1), p.121-123

2010

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Strong Correlation between the Expression Levels of HDAC4 and SIRT6 in Hematological Malignancies of the Adults

Pathology oncology research, 2017-07, Vol.23 (3), p.493-504

2017

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Pharmacometric Analysis of Intranasal and Intravenous Nalbuphine to Optimize Pain Management in Infants

Frontiers in pediatrics, 2022-03, Vol.10, p.837492

2022

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Is sperm hyaluronic acid binding ability predictive for clinical success of intracytoplasmic sperm injection: PICSI vs. ICSI?

Systems biology in reproductive medicine, 2014-12, Vol.60 (6), p.348-354

2014

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Expression Levels of Warburg-Effect Related microRNAs Correlate with each Other and that of Histone Deacetylase Enzymes in Adult Hematological Malignancies with Emphasis on Acute Myeloid Leukemia

Pathology oncology research, 2017, Vol.23 (1), p.207-216

2017

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Myosin phosphatase interacts with and dephosphorylates the retinoblastoma protein in THP-1 leukemic cells: Its inhibition is involved in the attenuation of daunorubicin-induced cell death by calyculin-A

Cellular signalling, 2008-11, Vol.20 (11), p.2059-2070

2008

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Subtelomeric 6.7Mb trisomy 10p and 5.6Mb monosomy 21q detected by FISH and array-CGH in three related patients

American journal of medical genetics. Part A, 2012-04, Vol.158A (4), p.869-876

2012

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Correlation study between sperm concentration, hyaluronic acid-binding capacity and sperm aneuploidy in Hungarian patients

Reproductive biomedicine online, 2012-12, Vol.25 (6), p.620-626

2012

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Cosmic muon detector using proportional chambers

European journal of physics, 2015-11, Vol.36 (6), p.1-10

2015

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Inborn error of cholesterol biosynthesis: Smith-Lemli-Opitz syndrome

Orvosi hetilap, 2015-10, Vol.156 (42), p.1695

2015

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Particle physics education in Hungary

Nuclear and particle physics proceedings, 2016-04, Vol.273-275, p.2569-2571

2016

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Blepharophimosis mental retardation syndrome Say‐Barber/Biesecker/Young‐Simpson type – New findings with neuroimaging

American journal of medical genetics. Part A, 2011-03, Vol.155 (3), p.634-637

2011

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Pharmacokinetics and tolerability of intranasal or intravenous administration of nalbuphine in infants

Archives of disease in childhood, 2023-01, Vol.108 (1), p.56-61

2023

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Research-based teaching at Wigner Research Centre for Physics, Hungary

Canadian journal of physics, 2020-06, Vol.98 (6), p.588-592

2020

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Cytotoxic drug sensitivity of Epstein-Barr virus transformed lymphoblastoid B-cells

BMC cancer, 2006-11, Vol.6 (1), p.265-265, Article 265

2006

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Endocrine and anatomical findings in a case of Solitary Median Maxillary Central Incisor Syndrome

European journal of medical genetics, 2012-02, Vol.55 (2), p.109-111

2012

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Variable expressivity of pfeiffer syndrome in a family with FGFR1 p.Pro252Arg mutation

De novo mutations of the gene encoding the histone acetyltransferase KAT6B in two patients with Say‐Barber/Biesecker/Young‐Simpson syndrome

Achondroplasia with multiple-suture craniosynostosis: A report of a new case of this rare association

Clinical and genetic characteristics of craniosynostosis in Hungary

The Wilms' tumour 1 gene as a factor in non-syndromic hypospadias: evidence and controversy

Effect of frequently used chemotherapeutic drugs on the cytotoxic activity of human natural killer cells

FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies

Lissencephaly and Band Heterotopia: LIS1, TUBA1A, and DCX Mutations in Hungary

Complete recovery from psychosis upon miglustat treatment in a juvenile Niemann–Pick C patient

A patient with Smith–Lemli–Opitz syndrome: novel mutation of the DHCR7 gene and effects of therapy with simvastatin and cholesterol supplement

Strong Correlation between the Expression Levels of HDAC4 and SIRT6 in Hematological Malignancies of the Adults

Pharmacometric Analysis of Intranasal and Intravenous Nalbuphine to Optimize Pain Management in Infants

Is sperm hyaluronic acid binding ability predictive for clinical success of intracytoplasmic sperm injection: PICSI vs. ICSI?

Expression Levels of Warburg-Effect Related microRNAs Correlate with each Other and that of Histone Deacetylase Enzymes in Adult Hematological Malignancies with Emphasis on Acute Myeloid Leukemia

Myosin phosphatase interacts with and dephosphorylates the retinoblastoma protein in THP-1 leukemic cells: Its inhibition is involved in the attenuation of daunorubicin-induced cell death by calyculin-A

Subtelomeric 6.7Mb trisomy 10p and 5.6Mb monosomy 21q detected by FISH and array-CGH in three related patients

Correlation study between sperm concentration, hyaluronic acid-binding capacity and sperm aneuploidy in Hungarian patients

Cosmic muon detector using proportional chambers

Inborn error of cholesterol biosynthesis: Smith-Lemli-Opitz syndrome

Particle physics education in Hungary

Blepharophimosis mental retardation syndrome Say‐Barber/Biesecker/Young‐Simpson type – New findings with neuroimaging

Pharmacokinetics and tolerability of intranasal or intravenous administration of nalbuphine in infants

Research-based teaching at Wigner Research Centre for Physics, Hungary

Cytotoxic drug sensitivity of Epstein-Barr virus transformed lymphoblastoid B-cells

Endocrine and anatomical findings in a case of Solitary Median Maxillary Central Incisor Syndrome

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