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329 results

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Page 1
Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia.
Brandes D, Yasin L, Nebral K, Ebler J, Schinnerl D, Picard D, Bergmann AK, Alam J, Köhrer S, Haas OA, Attarbaschi A, Marschall T, Stanulla M, Borkhardt A, Brozou T, Fischer U, Wagener R. Brandes D, et al. Among authors: haas oa. Hemasphere. 2023 Jul 17;7(8):e925. doi: 10.1097/HS9.0000000000000925. eCollection 2023 Aug. Hemasphere. 2023. PMID: 37469802 Free PMC article.
Prospective use of molecular minimal residual disease for risk stratification in children and adolescents with acute lymphoblastic leukemia : Long-term results of the AIEOP-BFM ALL 2000 trial in Austria.
Ronceray L, Dworzak M, Dieckmann K, Ebetsberger-Dachs G, Glogova E, Haas OA, Jones N, Nebral K, Moser R, Lion T, Meister B, Panzer-Grümayer R, Strehl S, Peters C, Pötschger U, Urban C, Mann G, Attarbaschi A; Austrian Berlin-Frankfurt-Münster (BFM) Study Group. Ronceray L, et al. Among authors: haas oa. Wien Klin Wochenschr. 2024 Jul;136(13-14):405-418. doi: 10.1007/s00508-023-02249-6. Epub 2023 Aug 3. Wien Klin Wochenschr. 2024. PMID: 37535134
Genomic breakpoint-specific monitoring of measurable residual disease in pediatric non-standard-risk acute myeloid leukemia.
Maurer-Granofszky M, Kohrer S, Fischer S, Schumich A, Nebral K, Larghero P, Meyer C, Mecklenbrauker A, Muhlegger N, Marschalek R, Haas OA, Panzer-Grumayer R, Dworzak MN. Maurer-Granofszky M, et al. Among authors: haas oa. Haematologica. 2024 Mar 1;109(3):740-750. doi: 10.3324/haematol.2022.282424. Haematologica. 2024. PMID: 37345487 Free PMC article.
Retrospective identification of the first cord blood-transplanted severe aplastic anemia in a STAT1-associated chronic mucocutaneous candidiasis family: case report, review of literature and pathophysiologic background.
Fink FM, Höpfl R, Witsch-Baumgartner M, Kropshofer G, Martin S, Fink V, Heeg M, Peters C, Zschocke J, Haas OA. Fink FM, et al. Among authors: haas oa. Front Immunol. 2024 Jul 24;15:1430938. doi: 10.3389/fimmu.2024.1430938. eCollection 2024. Front Immunol. 2024. PMID: 39114664 Free PMC article. Review.
Risk factors in DUX4-positive childhood and adolescent B-cell acute lymphoblastic leukemia.
Schinnerl D, Riebler M, Schumich A, Haslinger S, Bramböck A, Inthal A, Nykiel M, Maurer-Granofszky M, Haas OA, Pötschger U, Köhrer S, Nebral K, Dworzak MN, Attarbaschi A, Strehl S. Schinnerl D, et al. Among authors: haas oa. Blood Cancer J. 2024 Jul 22;14(1):119. doi: 10.1038/s41408-024-01099-3. Blood Cancer J. 2024. PMID: 39039054 Free PMC article.
Erratum to: Genomic breakpoint-specific monitoring of measurable residual disease in pediatric non-standard risk acute myeloid leukemia.
Maurer-Granofszky M, Köhrer S, Fischer S, Schumich A, Nebral K, Larghero P, Meyer C, Mecklenbräuker A, Mühlegger N, Marschalek R, Haas OA, Panzer-Grümayer R, Dworzak MN. Maurer-Granofszky M, et al. Among authors: haas oa. Haematologica. 2024 Jul 1;109(7):2379-2381. doi: 10.3324/haematol.2024.285153. Haematologica. 2024. PMID: 38946650 Free PMC article. No abstract available.
A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes.
Kager L, Jimenez-Heredia R, Zeitlhofer P, Novak W, Eder SK, Segarra-Roca A, Frohne A, Nebral K, Haimel M, Geyeregger R, Roetzer-Londgin K, Haas OA, Boztug K. Kager L, et al. Among authors: haas oa. Hemasphere. 2024 Jan 26;8(1):e31. doi: 10.1002/hem3.31. eCollection 2024 Jan. Hemasphere. 2024. PMID: 38434532 Free PMC article. No abstract available.
329 results