au.\*:("HAAS, O. A")
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Experience in pediatric myelodysplastic syndromesGADNER, H; HAAS, O. A.Hematology/oncology clinics of North America. 1992, Vol 6, Num 3, pp 655-672, issn 0889-8588Article
Hypothesis : meiotic origin of trisomic neoplasmsHAAS, O. A; SEYGER, M.Cancer genetics and cytogenetics. 1993, Vol 70, Num 2, pp 112-116, issn 0165-4608Article
Pure red cell aplasia as possible early manifestation of chronic myeloid leukemiaHAAS, O. A; HINTERBERGER, W; MORZ, R et al.American journal of hematology. 1988, Vol 27, Num 1, pp 20-25, issn 0361-8609Article
Parental origin of chromosomes involved in the translocation t(9;22)HAAS, O. A; ARGYRIOU-TIRITA, A; LION, T et al.Nature (London). 1992, Vol 359, Num 6394, pp 414-416, issn 0028-0836Article
Entscheidungshilfen zur Therapie der idiopathischen thrombozytopenischen Purpura (ITP) im Kindesalter = Guide du traitement du purpura thrombocytopénique chez l'enfant = Guide-lines for the therapy of idiopathic thrombocytopenic purpura in childhoodGADNER, H; GRUMAYER, E. R; HAAS, O. A et al.Klinische Pädiatrie. 1986, Vol 198, Num 4, pp 299-305, issn 0300-8630Article
Pathogenesis, biology, and management of myelodysplastic syndromes in childrenHAAS, O. A; GADNER, H.Seminars in hematology. 1996, Vol 33, Num 3, pp 225-235, issn 0037-1963Article
Noninvolvement of chromosome 16 in karyotype evolution of acute myeloid leukemia in a patient with a heritable fragile site on 16q22HAAS, O. A; NACHEVA, E; SCHWARZMEIER, J. D et al.Cancer genetics and cytogenetics. 1985, Vol 17, Num 1, pp 1-12, issn 0165-4608Article
Concurrent FOXP3- and CTLA4-associated genetic predisposition and skewed X chromosome inactivation in an autoimmune disease-prone familySEIDEL, M. G; RAMI, B; ITEM, C et al.European journal of endocrinology. 2012, Vol 167, Num 1, pp 131-134, issn 0804-4643, 4 p.Article
Fresh frozen plasma contains free asparagine and may replace the plasma asparagine pool during L-asparaginase therapySTEINER, M; ATTARBASCHI, A; HAAS, O. A et al.Leukemia. 2008, Vol 22, Num 6, pp 1290-1290, issn 0887-6924, 1 p.Article
Survival analysis and AML development in patients with de novo myelodysplastic syndromes: comparison of six different prognostic scoring systemsSPERR, W. R; WIMAZAL, F; VALENT, P et al.Annals of hematology (Print). 2001, Vol 80, Num 5, pp 272-277, issn 0939-5555Article
Elevated levels of lipoprotein(a) in familial bone marrow edema syndrome of the hipBERGER, C. E; KLUGER, R; URBAN, M et al.Clinical orthopaedics and related research. 2000, Num 377, pp 126-131, issn 0009-921XArticle
Heterogeneous TCR delta Vδ2-Dδ3 rearrangements and their relation to IgH and TCR gamma gene status in childhood B cell precursor leukaemiasKRESSLER, E; PANZER, S; GHALI, D. W et al.Leukemia research. 1999, Vol 23, Num 12, pp 1089-1096, issn 0145-2126Article
Competitive CBFβ/MYH11 reverse-transcriptase polymerase chain reaction for quantitative assessment of minimal residual disease during postremission therapy in acute myeloid leukemia with inversion(16) : A pilot studyLACZIKA, K; NOVAK, M; SCHWARZINGER, I et al.Journal of clinical oncology. 1998, Vol 16, Num 4, pp 1519-1525, issn 0732-183XArticle
Promoter-specific methylation and expression alterations of igf2 and h19 are involved in human hepatoblastomaLI, X; KOGNER, P; SANDSTEDT, B et al.International journal of cancer. 1998, Vol 75, Num 2, pp 176-180, issn 0020-7136Article
Donor leukocyte infusion for leukemic relapse after allogeneic marrow transplantation : Lack of residual donor hematopoiesis predicts aplasiaKEIL, F; HAAS, O. A; FRITSCH, G et al.Blood. 1997, Vol 89, Num 9, pp 3113-3117, issn 0006-4971Article
Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal : lack of gentoype/phenotype correlationsMEYER, J; SÜDBECK, P; LEROY, J. G et al.Human molecular genetics (Print). 1997, Vol 6, Num 1, pp 91-98, issn 0964-6906Article
Duration of second complete remission in patients with acute myeloid leukemia treated with chemotherapy : a retrospective single-center studyTHALHAMMER, F; GEISSLER, K; HAAS, O. A et al.Annals of hematology (Print). 1996, Vol 72, Num 4, pp 216-222, issn 0939-5555Article
MLL/ENL fusion in congenital acute lymphoblastic leukemia with a unique t(11;18;19)HORSTMANN, M; ARGYRIOU-TIRITA, A; BORKHARDT, A et al.Cancer genetics and cytogenetics. 1996, Vol 88, Num 2, pp 103-109, issn 0165-4608Article
Prognostic impact of karyotype and immunologic phenotype in 125 adult patients with de novo AMLMAROSI, C; KÖLLER, U; KREINER, G et al.Cancer genetics and cytogenetics. 1992, Vol 61, Num 1, pp 14-25, issn 0165-4608Article
Acute megakaryocytic leukemia in children : clinical, immunologic, and cytogenetic findings in two patientsSLAVC, I; URBAN, C; HAAS, O. A et al.Cancer. 1991, Vol 68, Num 10, pp 2266-2272, issn 0008-543XArticle
ITP in childhood: difficulties in the individual treatmentGRUMAYER, E. R; HAAS, O. A; PANZER, S et al.Klinische Pädiatrie. 1986, Vol 198, Num 5, pp 414-417, issn 0300-8630Article
ETV6/RUNX1 abrogates mitotic checkpoint function and targets its key player MAD2L1KRAPF, G; KAINDL, U; KILBEY, A et al.Oncogene (Basingstoke). 2010, Vol 29, Num 22, pp 3307-3312, issn 0950-9232, 6 p.Article
Comorbidity predicts survival in myelodysplastic syndromes or secondary acute myeloid leukaemia after allogeneic stem cell transplantationBOEHM, A; SPERR, W. R; RABITSCH, W et al.European journal of clinical investigation. 2008, Vol 38, Num 12, pp 945-952, issn 0014-2972, 8 p.Article
The MLL recombinome of acute leukemiasMEYER, C; SCHNEIDER, B; PIETERS, R et al.Leukemia. 2006, Vol 20, Num 5, pp 777-784, issn 0887-6924, 8 p.Article
High expression of the sister-chromatid separation regulator and proto-oncogene hSecurin occurs in a subset of myeloid leukaemias but is not implicated in the pathogenesis of aneuploidyAUNER, H. W; ZEBISCH, A; SCHIMEK, M. G et al.Leukemia. 2004, Vol 18, Num 2, pp 303-308, issn 0887-6924, 6 p.Article