Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

457 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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.
Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants.
Zipper L, Wagener R, Fischer U, Hoffmann A, Yasin L, Brandes D, Soura S, Anwar A, Walter C, Varghese J, Hauer J, Auer F, Bhatia S, Dugas M, Junk SV, Stanulla M, Haas OA, Borkhardt A, Reiff T, Brozou T. Zipper L, et al. Among authors: haas oa. Hemasphere. 2024 Jan 26;8(1):e26. doi: 10.1002/hem3.26. eCollection 2024 Jan. Hemasphere. 2024. PMID: 38434521 Free PMC article. No abstract available.
457 results