Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Cynthia A Delaat"'
Publikováno v:
Pediatric Research. 44:465-468
Hemophagocytic lymphohistiocytosis (HLH), also referred to as familial erythrophagocytic lymphohistiocytosis, is a rare disorder of infancy associated with proliferation of activated histiocytes and T cells, anemia, thrombocytopenia, and fevers. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8cfa0414955046330c4507aeca72b24
https://doi.org/10.1203/00006450-199810000-00001
https://doi.org/10.1203/00006450-199810000-00001
Autor:
Michael Steinbuch, Thomas G. Gross, Alexandra H. Filipovich, R. S. Shapiro, Cynthia A. DeLaat, Brett Loechelt, K. Scott Baker, Richard E. Harris
Publikováno v:
Blood. 89:3857-3863
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder of immune regulation leading to widespread lymphocytic and hemophagocytic infiltration of vital organs. Apparent cure has only been achieved with allogeneic bone marrow transplan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ed1394ce1f00d91156902613bd28c89
https://doi.org/10.1182/blood.v89.10.3857.3857_3857_3863
https://doi.org/10.1182/blood.v89.10.3857.3857_3857_3863
Autor:
K. Scott Baker, Cynthia A. DeLaat, Michael Steinbuch, Thomas G. Gross, Ralph S. Shapiro, Brett Loechelt, Richard Harris, Alexandra H. Filipovich
Publikováno v:
Blood. 89:3857-3863
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder of immune regulation leading to widespread lymphocytic and hemophagocytic infiltration of vital organs. Apparent cure has only been achieved with allogeneic bone marrow transplan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5354f8a7d2fb9f95b0a9ef7ada4ab172
https://doi.org/10.1182/blood.v89.10.3857
https://doi.org/10.1182/blood.v89.10.3857
Autor:
Mudra Kohli-Kumar, DJ Friedman, James Sambrano, R Mueller, Margaret Masterson, Claudia R. Morris, Cynthia A Delaat, K Desantes, Gregory A. Yanik, NT Shahidi
Publikováno v:
Blood. 84:2050-2054
Eighteen patients with Fanconi anemia (FA) with evidence of bone marrow (BM) aplasia underwent allogenic BM transplants (BMT) from matched sibling donors (MSD). Median age at BMT was 7.6 years. Conditioning consisted of low-dose cyclophosphamide (CY;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6814b0cb29f681e8fc1d09b541b24062
https://doi.org/10.1182/blood.v84.6.2050.2050
https://doi.org/10.1182/blood.v84.6.2050.2050
Autor:
Richard E. Harris, Mudra Kohli-Kumar, Christopher L Morris, Hal E. Broxmeyer, Margaret Masterson, Arleen D. Auerbach, Cynthia A Delaat, Nasorullah T. Shahidi, James Sambrano
Publikováno v:
British Journal of Haematology. 85:419-422
Summary There have only been a few reports documenting the use of umbilical cord blood as a source of stem cells for haemopoietic reconstitution. We report our experience with a child with Fanconi anaemia (FA) who underwent a stem cell transplant usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0145870976985d903c520eefe5d08d6b
https://doi.org/10.1111/j.1365-2141.1993.tb03192.x
https://doi.org/10.1111/j.1365-2141.1993.tb03192.x
Publikováno v:
Medical and Pediatric Oncology. 18:15-21
The acute leukemias have been considered to represent a clonal expansion of a malignant transformed hematopoietic progenitor cell with adherence to either the myeloid or lymphoid lineage—“lineage fidelity.” Lineage fidelity has been challenged
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d4a2a2552c99dcea48fc9a9ff431db6
https://doi.org/10.1002/mpo.2950180104
https://doi.org/10.1002/mpo.2950180104