Zobrazeno 1 - 10
of 33
pro vyhledávání: '"B Stollmann-Gibbels"'
Autor:
G. Nessler, A. R. Zander, E. N. Probst, B. Stollmann-Gibbels, E. M. Schneider, M. Dürken, Gritta Janka, D. Körholz, R. Bretz, H. Holsten-Griffin, R. Blütters-Sawatzki, E. Harps
Publikováno v:
Klinische Pädiatrie. 210:180-184
Hemophagocytic lymphohistiocytosis (HLH) is a rare disease of infancy and young childhood. The clinical presentation includes recurrent unexplained fever with hepatosplenomegaly. Cytopenia, hypofibrinogenemia and/or hypertriglyceridemia and hemophago
Autor:
Charlotte M. Niemeyer, B Stollmann-Gibbels, C. Bender-Götze, Martin Zimmermann, D. Körholz, J. Ritter, U. Creutzig
Publikováno v:
Leukemia. 12:652-659
To determine the role of intensive chemotherapy and allogeneic bone marrow transplantation (BMT) in treatment of refractory anemia with excess of blasts (RAEB) or RAEB-t (in transformation), the outcome of 37 consecutive children, 12 with RAEB and 25
Autor:
M, Dürken, E M, Schneider, R, Blütters-Sawatzki, B, Stollmann-Gibbels, G, Nessler, R, Bretz, D, Körholz, E N, Probst, H, Holsten-Griffin, E, Harps, A R, Zander, G E, Janka
Publikováno v:
Klinische Padiatrie. 210(4)
Hemophagocytic lymphohistiocytosis (HLH) is a rare disease of infancy and young childhood. The clinical presentation includes recurrent unexplained fever with hepatosplenomegaly. Cytopenia, hypofibrinogenemia and/or hypertriglyceridemia and hemophago
Autor:
Charlotte M. Niemeyer, J. Ritter, Jochen Harbott, I. Reinisch, U. Creutzig, Martin Zimmermann, B Stollmann-Gibbels
Publikováno v:
Acute Leukemias VI ISBN: 9783642643798
Recent reports estimate an approximately 20-fold higher incidence of leukemia in children with Down’s syndrome compared to non-Down’s syndrome children and a marked increase of the megakaryoblastic subtype (FAB M7)[l]. Twenty-six of 42 children w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e982fdf51415e86ac34f1689ba16773
https://doi.org/10.1007/978-3-642-60377-8_114
https://doi.org/10.1007/978-3-642-60377-8_114
Autor:
U, Creutzig, J, Ritter, J, Vormoor, W D, Ludwig, C, Niemeyer, I, Reinisch, B, Stollmann-Gibbels, M, Zimmermann, J, Harbott
Publikováno v:
Leukemia. 10(11)
Forty children with Down's syndrome have been identified among 633 patients in the cooperative pediatric BFM studies for acute myelogenous leukemia (AML) since 1987. The following features were characteristic for these patients: (1) a 500-fold higher
Publikováno v:
Leukemia. 7(10)
The karyotype of a boy with acute lymphoblastic leukemia (ALL) presenting with numerical and structural chromosome aberrations as determined by Giemsa-banding was further investigated using chromosome painting (CP). A translocation t(11;18)(q23;q21)
Autor:
U, Creutzig, C, Bender-Götze, T, Klingebiel, W, Ebell, W, Friedrich, B, Stollmann-Gibbels, H, Schmidt, M, Suttorp, A, Gratwohl, P, Heyen
Publikováno v:
Klinische Padiatrie. 204(4)
16 patients of studies AML-BFM-83 and -87 with allogeneic bone marrow transplantation (BMT) in first complete remission (CR) were compared with matched controls with postremission chemotherapy (CT-MC). CT-MC were selected from 250 non-grafted patient
Publikováno v:
Klinische Padiatrie. 204(4)
The myelodysplastic syndromes (MDS) are a group of hematopoietic neoplasms characterized by ineffective hematopoiesis and a high risk of transformation in acute leukemia. Pathogenesis and clinical course of these disorders are heterogenous. MDS is un
Autor:
E. van Weering, A. Gille, U. Creutzig, G. Kerndrup, B. Stollmann-Gibbels, Maurizio Aricò, Henrik Hasle, W Ebell, Andrea Biondi, E. van't Veer-Korhof, Georg Mann, A Cantù Rajnoldi, Guiseppe Basso, Susanna Fenu, Helmut Gadner, Oskar A. Haas, Martin Zimmermann, C.M. Niemeyer, G. Masera
Publikováno v:
Leukemia Research. 18:6
Autor:
G. Kardos, Rosalyn Slater, B. Stollmann-Gibbels, Martin Zimmermann, Jörg Ritter, Oskar A. Haas, H Ptoszkova, C. Fonatsch, Andrea Biondi, Georg Mann, Gitte Kerndrup, Jochen Harbott, Charlotte M. Niemeyer, Maurizio Aricò, J. Starý, Henrik Hasle, E. R. Van Wering, Guiseppe Basso, A Cantù Rajnoldi, Anna Maria Testi, Susanna Fenu, Ursula Creutzig
Publikováno v:
Scopus-Elsevier
We reviewed the clinical features, treatment, and outcome of 100 children with myelodysplastic syndrome (MDS), juvenile myelomonocytic leukemia (JMML), and acute myeloid leukemia (AML) associated with complete monosomy 7 (-7) or deletion of the long
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ff6e24a3d15e08ab74a43d6839b4c73
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033050457&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033050457&partnerID=MN8TOARS