Haas OA - Search Results

1

Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7. European Working Group on MDS in Childhood (EWOG-MDS).

Hasle H, Aricò M, Basso G, Biondi A, Cantù Rajnoldi A, Creutzig U, Fenu S, Fonatsch C, Haas OA, Harbott J, Kardos G, Kerndrup G, Mann G, Niemeyer CM, Ptoszkova H, Ritter J, Slater R, Starý J, Stollmann-Gibbels B, Testi AM, van Wering ER, Zimmermann M. Hasle H, et al. Among authors: haas oa. Leukemia. 1999 Mar;13(3):376-85. doi: 10.1038/sj.leu.2401342. Leukemia. 1999. PMID: 10086728

2

Minimal requirements for the diagnosis, classification, and evaluation of the treatment of childhood acute lymphoblastic leukemia (ALL) in the "BFM Family" Cooperative Group.

van der Does-van den Berg A, Bartram CR, Basso G, Benoit YC, Biondi A, Debatin KM, Haas OA, Harbott J, Kamps WA, Köller U, et al. van der Does-van den Berg A, et al. Among authors: haas oa. Med Pediatr Oncol. 1992;20(6):497-505. doi: 10.1002/mpo.2950200603. Med Pediatr Oncol. 1992. PMID: 1435520

3

The translocation t(1;22)(p13;q13) is a nonrandom marker specifically associated with acute megakaryocytic leukemia in young children.

Lion T, Haas OA, Harbott J, Bannier E, Ritterbach J, Jankovic M, Fink FM, Stojimirovic A, Herrmann J, Riehm HJ, et al. Lion T, et al. Among authors: haas oa. Blood. 1992 Jun 15;79(12):3325-30. Blood. 1992. PMID: 1596573 Free article.

4

Trisomy 4: a specific karyotype anomaly in primary and secondary acute myeloid leukemia.

Weber E, Nowotny H, Haas OA, Kasparu H, Grois N, Lutz D. Weber E, et al. Among authors: haas oa. Leukemia. 1990 Mar;4(3):219-21. Leukemia. 1990. PMID: 2179639 Review.

5

Phenotypic and genotypic heterogeneity in infant acute leukemia. I. Acute lymphoblastic leukemia.

Ludwig WD, Bartram CR, Harbott J, Köller U, Haas OA, Hansen-Hagge T, Heil G, Seibt-Jung H, Teichmann JV, Ritter J, et al. Ludwig WD, et al. Among authors: haas oa. Leukemia. 1989 Jun;3(6):431-9. Leukemia. 1989. PMID: 2725059

6

Phenotypic and genotypic heterogeneity in infant acute leukemia. II. Acute nonlymphoblastic leukemia.

Köller U, Haas OA, Ludwig WD, Bartram CR, Harbott J, Panzer-Grümayer R, Hansen-Hagge T, Ritter J, Creutzig U, Knapp W, et al. Köller U, et al. Among authors: haas oa. Leukemia. 1989 Oct;3(10):708-14. Leukemia. 1989. PMID: 2779287

7

A novel type of MLL/AF10 fusion transcript in a child with acute megakaryocytic leukemia (AML-M7).

Borkhardt A, Haas OA, Strobl W, Repp R, Mann G, Gadner H, Lampert F. Borkhardt A, et al. Among authors: haas oa. Leukemia. 1995 Oct;9(10):1796-7. Leukemia. 1995. PMID: 7564531 No abstract available.

8

Acute megakaryocytic leukemia with the t(1;22)(p13;q13).

Lion T, Haas OA. Lion T, et al. Among authors: haas oa. Leuk Lymphoma. 1993 Sep;11(1-2):15-20. doi: 10.3109/10428199309054726. Leuk Lymphoma. 1993. PMID: 8220150 Review.

9

Expression of identical E2A/PBX1 fusion transcripts occurs in both pre-B and early pre-B immunological subtypes of childhood acute lymphoblastic leukemia.

Izraeli S, Henn T, Strobl H, Ludwig WD, Kovar H, Haas OA, Harbott J, Bartram CR, Gadner H, Lion T. Izraeli S, et al. Among authors: haas oa. Leukemia. 1993 Dec;7(12):2054-6. Leukemia. 1993. PMID: 8255105

10

Detection and clinical relevance of genetic abnormalities in pediatric acute lymphoblastic leukemia: a comparison between cytogenetic and polymerase chain reaction analyses.

Izraeli S, Janssen JW, Haas OA, Harbott J, Brok-Simoni F, Walther JU, Kovar H, Henn T, Ludwig WD, Reiter A, et al. Izraeli S, et al. Among authors: haas oa. Leukemia. 1993 May;7(5):671-8. Leukemia. 1993. PMID: 8483319

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