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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2005 1
2006 2
2007 1
2008 2
2012 3
2013 3
2014 2
2015 2
2017 1
2018 5
2019 4
2020 4
2021 4
2022 3
2023 3
2024 0

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37 results

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Page 1
Next-Generation Sequencing-Based Genomic Profiling of Children with Acute Myeloid Leukemia.
Krizsán S, Péterffy B, Egyed B, Nagy T, Sebestyén E, Hegyi LL, Jakab Z, Erdélyi DJ, Müller J, Péter G, Csanádi K, Kállay K, Kriván G, Barna G, Bedics G, Haltrich I, Ottóffy G, Csernus K, Vojcek Á, Tiszlavicz LG, Gábor KM, Kelemen Á, Hauser P, Gaál Z, Szegedi I, Ujfalusi A, Kajtár B, Kiss C, Matolcsy A, Tímár B, Kovács G, Alpár D, Bödör C. Krizsán S, et al. Among authors: haltrich i. J Mol Diagn. 2023 Aug;25(8):555-568. doi: 10.1016/j.jmoldx.2023.04.004. Epub 2023 Apr 22. J Mol Diagn. 2023. PMID: 37088137 Free PMC article.
[Clinical aspects of 22q11.2 microdeletion syndrome].
Szumutku F, Kádár K, Kovács ÁF, Lengyel A, Pinti É, Némethi Z, Abonyi T, Csáky-Szunyogh M, Fekete G, Haltrich I. Szumutku F, et al. Among authors: haltrich i. Orv Hetil. 2022 Jan 2;163(1):21-30. doi: 10.1556/650.2022.32299. Print 2022 Jan 2. Orv Hetil. 2022. PMID: 34974426 Hungarian.
PersonALL: a genetic scoring guide for personalized risk assessment in pediatric B-cell precursor acute lymphoblastic leukemia.
Bedics G, Egyed B, Kotmayer L, Benard-Slagter A, de Groot K, Bekő A, Hegyi LL, Bátai B, Krizsán S, Kriván G, Erdélyi DJ, Müller J, Haltrich I, Kajtár B, Pajor L, Vojcek Á, Ottóffy G, Ujfalusi A, Szegedi I, Tiszlavicz LG, Bartyik K, Csanádi K, Péter G, Simon R, Hauser P, Kelemen Á, Sebestyén E, Jakab Z, Matolcsy A, Kiss C, Kovács G, Savola S, Bödör C, Alpár D. Bedics G, et al. Among authors: haltrich i. Br J Cancer. 2023 Aug;129(3):455-465. doi: 10.1038/s41416-023-02309-8. Epub 2023 Jun 21. Br J Cancer. 2023. PMID: 37340093 Free PMC article.
[Examination of sex chromosome abnormalities in childhood].
Pinti É, Lengyel A, Sallai Á, Fekete G, Haltrich I. Pinti É, et al. Among authors: haltrich i. Orv Hetil. 2018 Jul;159(27):1121-1128. doi: 10.1556/650.2018.31081. Orv Hetil. 2018. PMID: 29961370 Hungarian.
Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature.
Lengyel A, Pinti É, Pikó H, Jávorszky E, David D, Tihanyi M, Gönczi É, Kiss E, Tóth Z, Tory K, Fekete G, Haltrich I. Lengyel A, et al. Among authors: haltrich i. Eur J Med Genet. 2020 Oct;63(10):104027. doi: 10.1016/j.ejmg.2020.104027. Epub 2020 Aug 3. Eur J Med Genet. 2020. PMID: 32758661 Free article. Review.
Hypodiploidy has unfavorable impact on survival in pediatric acute myeloid leukemia: an I-BFM Study Group collaboration.
Hammer ASB, Juul-Dam KL, Sandahl JD, Abrahamsson J, Czogala M, Delabesse E, Haltrich I, Jahnukainen K, Kolb EA, Kovács G, Leverger G, Locatelli F, Masetti R, Noren-Nyström U, Raimondi SC, Rasche M, Reinhardt D, Taki T, Tomizawa D, Zeller B, Hasle H, Kjeldsen E. Hammer ASB, et al. Among authors: haltrich i. Blood Adv. 2023 Mar 28;7(6):1045-1055. doi: 10.1182/bloodadvances.2022008251. Blood Adv. 2023. PMID: 36332007 Free PMC article.
37 results