Bessenyei B - Search Results

1

[Results of clinical and genetic diagnosis of rare diseases in the Eastern region of Hungary (2007-2013)].

Szakszon K, Balogh E, Ujfalusi A, Bessenyei B, P Szabó G, Balogh I, Oláh E. Szakszon K, et al. Among authors: bessenyei b. Orv Hetil. 2014 Mar 2;155(9):348-57. doi: 10.1556/OH.2014.29690. Orv Hetil. 2014. PMID: 24566699 Hungarian.

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

[Expression of ZEBRA protein of Epstein-Barr virus in Hungarian patients with Hodgkin lymphoma: latent or lytic cycle?].

Beck Z, Illés A, Keresztes K, Bessenyei B, Szöllosi Z, Kis A, Oláh E. Beck Z, et al. Among authors: bessenyei b. Orv Hetil. 2006 Aug 20;147(33):1539-44. Orv Hetil. 2006. PMID: 17037676 Hungarian.

5

[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.

6

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

7

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

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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