Zobrazeno 1 - 10
of 242
pro vyhledávání: '"S S, Winter"'
Autor:
S Gupta, M Devidas, M L Loh, E A Raetz, S Chen, C Wang, P Brown, A J Carroll, N A Heerema, J M Gastier-Foster, K P Dunsmore, E C Larsen, K W Maloney, L A Mattano, S S Winter, N J Winick, W L Carroll, S P Hunger, M Borowitz, B L Wood
Publikováno v:
Leukemia.
Autor:
Manjit Hanspal, Scott J. Yi, James Murray, S. S. Winter, Hani Hassoun, J. N. Vassiliadis, R. E. Ware, Jiri Palek, Shyh-Shin Chiou
Publikováno v:
Journal of Clinical Investigation. 96:2623-2629
We describe a spectrin variant characterized by a truncated beta chain and associated with hereditary spherocytosis. The clinical phenotype consists of a moderate hemolytic anemia with striking spherocytosis and mild spiculation of the red cells. We
Publikováno v:
British journal of haematology. 115(4)
The bone marrow (BM) microenvironment supports leukaemia cell survival and proliferation. The roles played by adhesive receptor interactions in the survival of T-lineage acute lymphoblastic leukaemia (T-ALL) cells on BM stromal cells are not well und
Publikováno v:
Cytometry. 40(1)
The ex vivo survival of leukemic cells maintained on bone marrow stroma is an important tool for the investigation of cell survival and leukemogenesis. Currently, ex vivo survival of leukemic cell survival is measured by coculture on stromal cell mon
Publikováno v:
Adolescent medicine (Philadelphia, Pa.). 10(3)
Myelodysplastic syndromes (MDS) are a group of acquired blood diseases that are the result of abnormal bone marrow function. The ineffective production of red cells, platelets, and white blood cells can lead to symptomatic anemia, bruising, infection
Publikováno v:
Pharmacotherapy. 17(5)
We evaluated the analgesic efficacy of EMLA cream after repeated bone marrow aspirations or lumbar punctures (LPs) in children with cancer, and compared the ratings among patients, their parents, physicians, and nurses. Data from LPs were analyzed at
Publikováno v:
Medical and pediatric oncology. 28(1)
The term myelodysplasia (MDS) refers to a group of bone marrow failure syndromes which are relatively rare in childhood. The pathogenesis of MDS is unknown, but a variety of chromosomal, molecular, and cytochemical abnormalities have been reported. W
Publikováno v:
Medical and pediatric oncology. 26(1)
Castleman's disease (CD) is a lymphoproliferative disorder characterized by enlarged hyperplastic lymph nodes. CD may be localized or multifocal, and is often associated with signs and symptoms of generalized inflammation. The systemic manifestations
Publikováno v:
The Journal of pediatrics. 125(5 Pt 1)
Ultrasonographic records of 75 children with sickle cell disease and hepatobiliary symptoms were reviewed. Seventeen had gallbladder sludge, nine with concurrent stones and eight with sludge alone. Because all the children eventually had gallstones,
Publikováno v:
Journal of Investigative Medicine. 53:S166.1-S166
Transient myeloproliferative disorder (“TMD”) with or without progression to acute megakaryocytic leukemia (“AMKL”) has been reported in association with Down syndrome (“DS”) for the past 40 years. To date, 29 cases of TMD have been repor