Bessenyei B - Search Results

1

Clinical and genetic characteristics of craniosynostosis in Hungary.

Bessenyei B, Nagy A, Szakszon K, Mokánszki A, Balogh E, Ujfalusi A, Tihanyi M, Novák L, Bognár L, Oláh É. Bessenyei B, et al. Am J Med Genet A. 2015 Dec;167A(12):2985-91. doi: 10.1002/ajmg.a.37298. Epub 2015 Aug 20. Am J Med Genet A. 2015. PMID: 26289989

2

[Association of Hodgkin lymphoma with Epstein-Barr virus in Hungary].

Keresztes K, Bessenyei B, Szöllosi Z, Beck Z, Miltényi Z, Nemes Z, Oláh E, Illés A. Keresztes K, et al. Among authors: bessenyei b. Orv Hetil. 2005 Jul 24;146(30):1575-82. Orv Hetil. 2005. PMID: 16136734 Hungarian.

3

Association between the Epstein-Barr virus and Hodgkin's lymphoma in the North-Eastern part of Hungary: effects on therapy and survival.

Keresztes K, Miltenyi Z, Bessenyei B, Beck Z, Szollosi Z, Nemes Z, Olah E, Illes A. Keresztes K, et al. Among authors: bessenyei b. Acta Haematol. 2006;116(2):101-7. doi: 10.1159/000093639. Acta Haematol. 2006. PMID: 16914904

4

[Detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation].

Szabó GP, Bessenyei B, Balogh E, Ujfalusi A, Szakszon K, Oláh E. Szabó GP, et al. Among authors: bessenyei b. Orv Hetil. 2010 Jul 4;151(27):1091-8. doi: 10.1556/OH.2010.28911. Orv Hetil. 2010. PMID: 20558358 Hungarian.

5

Blepharophimosis mental retardation syndrome Say-Barber/Biesecker/Young-Simpson type - new findings with neuroimaging.

Szakszon K, Berényi E, Jakab A, Bessenyei B, Balogh E, Köbling T, Szilvássy J, Knegt AC, Oláh E. Szakszon K, et al. Among authors: bessenyei b. Am J Med Genet A. 2011 Mar;155A(3):634-7. doi: 10.1002/ajmg.a.33837. Epub 2011 Feb 22. Am J Med Genet A. 2011. PMID: 21344633

6

Jumping translocation of chromosome 1q associated with good clinical outcome in a case of Burkitt leukemia.

Bessenyei B, Ujfalusi A, Balogh E, Olah E, Szegedi I, Kiss C. Bessenyei B, et al. Cancer Genet. 2011 Apr;204(4):207-10. doi: 10.1016/j.cancergencyto.2010.10.005. Cancer Genet. 2011. PMID: 21536239

7

New mutations in the ATM gene and clinical data of 25 AT patients.

Demuth I, Dutrannoy V, Marques W Jr, Neitzel H, Schindler D, Dimova PS, Chrzanowska KH, Bojinova V, Gregorek H, Graul-Neumann LM, von Moers A, Schulze I, Nicke M, Bora E, Cankaya T, Oláh É, Kiss C, Bessenyei B, Szakszon K, Gruber-Sedlmayr U, Kroisel PM, Sodia S, Goecke TO, Dörk T, Digweed M, Sperling K, de Sá J, Lourenco CM, Varon R. Demuth I, et al. Among authors: bessenyei b. Neurogenetics. 2011 Nov;12(4):273-82. doi: 10.1007/s10048-011-0299-0. Epub 2011 Oct 2. Neurogenetics. 2011. PMID: 21965147

8

Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary.

Mokánszki A, Körhegyi I, Szabó N, Bereg E, Gergev G, Balogh E, Bessenyei B, Sümegi A, Morris-Rosendahl DJ, Sztriha L, Oláh E. Mokánszki A, et al. Among authors: bessenyei b. J Child Neurol. 2012 Dec;27(12):1534-40. doi: 10.1177/0883073811436326. Epub 2012 Mar 8. J Child Neurol. 2012. PMID: 22408144

9

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

Bessenyei B, Nagy A, Balogh E, Novák L, Bognár L, Knegt AC, Oláh E. Bessenyei B, et al. Am J Med Genet A. 2013 Oct;161A(10):2641-4. doi: 10.1002/ajmg.a.36130. Epub 2013 Aug 15. Am J Med Genet A. 2013. PMID: 23949953

10

[Clinical and genetic characteristics of craniosynostosis].

Bessenyei B, Oláh E. Bessenyei B, et al. Orv Hetil. 2014 Mar 2;155(9):341-7. doi: 10.1556/OH.2014.29821. Orv Hetil. 2014. PMID: 24566698 Review. Hungarian.

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