Benyó G - Search Results

1

Chromosomal breakage tests in the differential diagnosis of Fanconi anemia and aplastic anemia.

Farkas G, Székely G, Goda V, Kállay KM, Kocsis ZS, Szakszon K, Benyó G, Erdélyi D, Liptai Z, Csordás K, Kertész G, Szegedi I, Kriván G, Takácsi-Nagy Z, Polgár C, Jurányi Z. Farkas G, et al. Among authors: benyo g. Eur J Haematol. 2023 Aug;111(2):254-262. doi: 10.1111/ejh.13990. Epub 2023 May 16. Eur J Haematol. 2023. PMID: 37194391

2

Successful unrelated umbilical cord blood transplantation in Lesch-Nyhan syndrome.

Kállay K, Liptai Z, Benyó G, Kassa C, Goda V, Sinkó J, Tóth A, Kriván G. Kállay K, et al. Among authors: benyo g. Metab Brain Dis. 2012 Jun;27(2):193-6. doi: 10.1007/s11011-012-9279-9. Epub 2012 Feb 17. Metab Brain Dis. 2012. PMID: 22350962

3

Antithymocyte Globuline Therapy and Bradycardia in Children.

Kállay K, Zakariás D, Csordás K, Benyó G, Kassa C, Sinkó J, Stréhn A, Horváth O, Vásárhelyi B, Kriván G. Kállay K, et al. Among authors: benyo g. Pathol Oncol Res. 2019 Apr;25(2):487-492. doi: 10.1007/s12253-018-0403-y. Epub 2018 Mar 9. Pathol Oncol Res. 2019. PMID: 29524166 Free article.

4

Successful umbilical cord blood stem cell transplantation in a child with WHIM syndrome.

Kriván G, Erdos M, Kállay K, Benyó G, Tóth A, Sinkó J, Goda V, Tóth B, Maródi L. Kriván G, et al. Among authors: benyo g. Eur J Haematol. 2010 Mar;84(3):274-5. doi: 10.1111/j.1600-0609.2009.01368.x. Epub 2009 Oct 29. Eur J Haematol. 2010. PMID: 19878273 No abstract available.

5

[Successful autologous haematopoietic stem cell transplantation in severe, therapy-resistant childhood Crohn's disease. Report on the first case in Hungary].

Kriván G, Szabó D, Kállay K, Benyó G, Kassa C, Sinkó J, Goda V, Arató A, Veres G. Kriván G, et al. Among authors: benyo g. Orv Hetil. 2014 May 18;155(20):789-92. doi: 10.1556/OH.2014.29892. Orv Hetil. 2014. PMID: 24819188 Hungarian.

6

Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree.

Tawana K, Wang J, Király PA, Kállay K, Benyó G, Zombori M, Csomor J, Al Seraihi A, Rio-Machin A, Matolcsy A, Chelala C, Cavenagh J, Fitzgibbon J, Bödör C. Tawana K, et al. Among authors: benyo g. Eur J Hum Genet. 2017 Aug;25(8):1020-1024. doi: 10.1038/ejhg.2017.80. Epub 2017 May 17. Eur J Hum Genet. 2017. PMID: 28513614 Free PMC article.

7

[Clinical and genetic background of familial myelodysplasia and acute myeloid leukemia].

Király PA, Kállay K, Marosvári D, Benyó G, Szőke A, Csomor J, Bödör C. Király PA, et al. Among authors: benyo g. Orv Hetil. 2016 Feb 21;157(8):283-9. doi: 10.1556/650.2016.30375. Orv Hetil. 2016. PMID: 26876264 Review. Hungarian.

8

Claudin-1 and claudin-2 differentiate fetal and embryonal components in human hepatoblastoma.

Halász J, Holczbauer A, Páska C, Kovács M, Benyó G, Verebély T, Schaff Z, Kiss A. Halász J, et al. Among authors: benyo g. Hum Pathol. 2006 May;37(5):555-61. doi: 10.1016/j.humpath.2005.12.015. Hum Pathol. 2006. PMID: 16647953

9

Evaluation of the good tumor response of embryonal tumor with abundant neuropil and true rosettes (ETANTR).

Mozes P, Hauser P, Hortobágyi T, Benyó G, Peták I, Garami M, Cserháti A, Bartyik K, Bognár L, Nagy Z, Turányi E, Hideghéty K. Mozes P, et al. Among authors: benyo g. J Neurooncol. 2016 Jan;126(1):99-105. doi: 10.1007/s11060-015-1938-3. Epub 2015 Sep 15. J Neurooncol. 2016. PMID: 26373296 Review.

10

[Arthrogryposis–renal dysfunction–cholestasis syndrome].

Mikó Á, Lóth S, Müller J, Lotz B, Rossitto P, Szabolcs A, Benyó G, Jávorszky E, Tory K, Dezsőfi A. Mikó Á, et al. Among authors: benyo g. Orv Hetil. 2022 Jan 9;163(2):74-78. doi: 10.1556/650.2022.32312. Print 2022 Jan 9. Orv Hetil. 2022. PMID: 34999573 Hungarian.

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