Oláh E - Search Results

1

[Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].

Szabó Gabriella P, Balogh E, Jakab Z, Germán P, Bodnár F, Kiss A, Telek B, Oláh E. Szabó Gabriella P, et al. Among authors: olah e. Orv Hetil. 2002 Dec 15;143(50):2775-9. Orv Hetil. 2002. PMID: 12583317 Hungarian.

2

[Study of pathogenetic role of Epstein-Barr virus in Hungarian patients with B-cell non-Hodgkin lymphomas].

Germán P, Beck Z, Semsei I, Kiss S, Görög B, Balogh E, Tóth F, Nemes Z, Pajor L, Oláh E. Germán P, et al. Among authors: olah e. Orv Hetil. 2002 Nov 24;143(47):2619-24. Orv Hetil. 2002. PMID: 12532647 Review. Hungarian.

3

[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: olah e. Orv Hetil. 2010 Jul 4;151(27):1091-8. doi: 10.1556/OH.2010.28911. Orv Hetil. 2010. PMID: 20558358 Hungarian.

4

[Cerebral glucose metabolism in Down syndrome using positron emission tomography].

Balogh E, Lengyel Z, Emri M, Szikszai E, Esik O, Kollár J, Sikula J, Trón L, Oláh E. Balogh E, et al. Among authors: olah e. Orv Hetil. 2002 May 26;143(21 Suppl 3):1304-7. Orv Hetil. 2002. PMID: 12077923 Hungarian.

5

[Immunohistochemical demonstration of mutant nucleophosmin in acute myeloid leukemia: biological and clinical features related to NPMc expression].

Bedekovics J, Rejto L, Telek B, Udvardy M, Ujfalusi A, Oláh E, Hevessy Z, Kappelmayer J, Kajtár B, Méhes G. Bedekovics J, et al. Among authors: olah e. Orv Hetil. 2009 May 31;150(22):1031-5. doi: 10.1556/OH.2009.28623. Orv Hetil. 2009. PMID: 19465351 Hungarian.

6

[Citogenetic and molecular genetic studies in infertility in eastern Hungary].

Mokánszki A, Ujfalusi A, Balogh E, Molnár Z, Sápy T, Jakab A, Varga A, Oláh E. Mokánszki A, et al. Among authors: olah e. Orv Hetil. 2013 Jan 13;154(2):52-61. doi: 10.1556/OH.2013.29510. Orv Hetil. 2013. PMID: 23291203 Hungarian.

7

[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: olah e. Orv Hetil. 2014 Mar 2;155(9):348-57. doi: 10.1556/OH.2014.29690. Orv Hetil. 2014. PMID: 24566699 Hungarian.

8

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

Szabó GP, Knegt AC, Ujfalusi A, Balogh E, Szabó T, Oláh É. Szabó GP, et al. Among authors: olah e. Am J Med Genet A. 2012 Apr;158A(4):869-76. doi: 10.1002/ajmg.a.35236. Epub 2012 Mar 9. Am J Med Genet A. 2012. PMID: 22407767

9

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. Among authors: olah e. Cancer Genet. 2011 Apr;204(4):207-10. doi: 10.1016/j.cancergencyto.2010.10.005. Cancer Genet. 2011. PMID: 21536239

10

Variant translocations of 11q23 in infant acute lymphoblastic leukemia (ALL): do outcomes differ from t(4;11)?

Jakab Z, Balogh E, Karászi E, Kappelmayer J, Kiss C, Oláh E. Jakab Z, et al. Among authors: olah e. Med Pediatr Oncol. 2002 Jul;39(1):63-5. doi: 10.1002/mpo.10047. Med Pediatr Oncol. 2002. PMID: 12116086 No abstract available.

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