Publications by authors named "Eva Olah"

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FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies.
László Madar, Katalin Szakszon, György Pfliegler, Gabriella P Szabó, Boglárka Brúgós

J Biotechnol· August 2019

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

Pathology· June 2018

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Nucleotide Transition 390C-T in the Wilms' Tumor 1 Gene: A Risk Factor of Hypospadias?
Gergely Buglyó, Ágnes Magyar, Sándor Biró, István Csízy, Dániel Beyer

Curr Urol· August 2017

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Strong Correlation between the Expression Levels of HDAC4 and SIRT6 in Hematological Malignancies of the Adults.
Zsuzsanna Gaál, Éva Oláh, László Rejtő, Ferenc Erdődi, László Csernoch

Pathol Oncol Res· July 2017

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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.
Zsuzsanna Gaál, Éva Oláh, László Rejtő, Bálint László Bálint, László Csernoch

Pathol Oncol Res· January 2017

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Clinical and genetic characteristics of craniosynostosis in Hungary.
Beáta Bessenyei, Andrea Nagy, Katalin Szakszon, Attila Mokánszki, Erzsébet Balogh

Am J Med Genet A· December 2015

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[Inborn error of cholesterol biosynthesis: Smith-Lemli-Opitz syndrome].
Katalin Koczok, Anna V Oláh, Gabriella P Szabó, Éva Oláh, Olga Török

Orv Hetil· October 2015

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Is sperm hyaluronic acid binding ability predictive for clinical success of intracytoplasmic sperm injection: PICSI vs. ICSI?
Attila Mokánszki, Emese Varga Tóthné, Béla Bodnár, Zoltán Tándor, Zsuzsanna Molnár

Syst Biol Reprod Med· December 2014

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Variable expressivity of pfeiffer syndrome in a family with FGFR1 p.Pro252Arg mutation.
Beáta Bessenyei, Mariann Tihanyi, Marianna Hartwig, Katalin Szakszon, Éva Oláh

Am J Med Genet A· December 2014

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[Epigenetic regulatory mechanisms and their disorders in leukemia].
Zsuzsanna Gaál, Eva Oláh

Magy Onkol· June 2014

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[Editor's commentary. Rare diseases in Hungary].
Eva Oláh

Orv Hetil· March 2014

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[Clinical and genetic characteristics of craniosynostosis].
Beáta Bessenyei, Eva Oláh

Orv Hetil· March 2014

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

Orv Hetil· March 2014

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Complete recovery from psychosis upon miglustat treatment in a juvenile Niemann-Pick C patient.
Katalin Szakszon, István Szegedi, Agnes Magyar, Eva Oláh, Mónika Andrejkovics

Eur J Paediatr Neurol· January 2014

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Achondroplasia with multiple-suture craniosynostosis: a report of a new case of this rare association.
Beáta Bessenyei, Andrea Nagy, Erzsébet Balogh, László Novák, László Bognár

Am J Med Genet A· October 2013

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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.
Katalin Szakszon, Carmelo Salpietro, Naseebullah Kakar, Alida C Knegt, Éva Oláh

Am J Med Genet A· April 2013

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[Citogenetic and molecular genetic studies in infertility in eastern Hungary].
Attila Mokánszki, Anikó Ujfalusi, Erzsébet Balogh, Zsuzsanna Molnár, Tamás Sápy

Orv Hetil· January 2013

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Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary.
Attila Mokánszki, Ivett Körhegyi, Nóra Szabó, Edit Bereg, Gyurgyinka Gergev

J Child Neurol· December 2012

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Correlation study between sperm concentration, hyaluronic acid-binding capacity and sperm aneuploidy in Hungarian patients.
Attila Mokánszki, Zsuzsanna Molnár, Anikó Ujfalusi, Erzsébet Balogh, Zsuzsa Kassai Bazsáné

Reprod Biomed Online· December 2012

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[MicroRNA-s and their role in malignant hematologic diseases].
Zsuzsanna Gaál, Eva Oláh

Orv Hetil· December 2012

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Meiotic segregation study of a novel t(3;6)(q21;q23) in an infertile man using fluorescence in situ hybridization (FISH).
Attila Mokánszki, Anikó Ujfalusi, Erzsébet Balogh, Andrea Sümegi, Péter Antal-Szalmás

Syst Biol Reprod Med· June 2012

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Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients.
Gabriella P Szabó, Alida C Knegt, Anikó Ujfalusi, Erzsébet Balogh, Tamás Szabó

Am J Med Genet A· April 2012

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Endocrine and anatomical findings in a case of Solitary Median Maxillary Central Incisor Syndrome.
Katalin Szakszon, Enikő Felszeghy, István Csízy, Tamás Józsa, Rita Káposzta

Eur J Med Genet· February 2012

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New mutations in the ATM gene and clinical data of 25 AT patients.
Ilja Demuth, Véronique Dutrannoy, Wilson Marques, Heidemarie Neitzel, Detlev Schindler

Neurogenetics· November 2011

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Jumping translocation of chromosome 1q associated with good clinical outcome in a case of Burkitt leukemia.
Beata Bessenyei, Aniko Ujfalusi, Erzsebet Balogh, Eva Olah, Istvan Szegedi

Cancer Genet· April 2011

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