Found: 12
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Recombinant human granulocyte-colony-stimulating factor in the treatment of patients with chronic benign granulocytopenia and congenital agranulocytosis (Kostmann's syndrome).
- Published in:
- 1992
- By:
- Publication type:
- journal article
HUMAN LYMPHOCYTE SUBPOPULATIONS. HUMAN THYMUS-LYMPHOID TISSUE (HTL) ANTIGEN-POSITIVE LYMPHOCYTES FORMING ROSETTES WITH SHEEP ERYTHROCYTES AND HTL ANTIGEN-NEGATIVE LYMPHOCYTES INTERACTING WITH ANTIGEN-ANTIBODY-COMPLEMENT COMPLEXES.
- Published in:
- Clinical & Experimental Immunology, 1973, v. 14, n. 3, p. 319
- By:
- Publication type:
- Article
HUMAN THYMUS LYMPHOID TISSUE (HTL) ANTIGEN, COMPLEMENT RECEPTOR AND ROSETTE FORMATION WITH SHEEP ERYTHROCYTES OF THE LYMPHOCYTES FROM PRIMARY IMMUNODEFICIENCY DISEASES.
- Published in:
- Clinical & Experimental Immunology, 1973, v. 14, n. 3, p. 309
- By:
- Publication type:
- Article
Clinicopathologic characteristics of leukemia in Japanese children and young adults.
- Published in:
- 2001
- By:
- Publication type:
- journal article
An effective chemotherapeutic regimen for acute myeloid leukemia and myelodysplastic syndrome in children with Down's syndrome.
- Published in:
- 2000
- By:
- Publication type:
- journal article
Pancreatic carcinoma in children in Japan.
- Published in:
- 1973
- By:
- Publication type:
- journal article
Hereditary hemochromatosis not associated with common HFE gene mutation in Japanese siblings.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Hematopoietic stem cell transplantation for Diamond-Blackfan anemia: A report from the Aplastic Anemia Committee of the Japanese Society of Pediatric Hematology.
- Published in:
- Pediatric Transplantation, 2007, v. 11, n. 6, p. 601, doi. 10.1111/j.1399-3046.2006.00616.x
- By:
- Publication type:
- Article
Granulocyte Transfusion in Japanese Children.
- Published in:
- Transfusion, 2001, v. 41, p. 94S
- By:
- Publication type:
- Article
High expression of EVI1 and MEL1 is a compelling poor prognostic marker of pediatric AML.
- Published in:
- Leukemia (08876924), 2015, v. 29, n. 5, p. 1076, doi. 10.1038/leu.2015.5
- By:
- Publication type:
- Article
N822 mutation of KIT gene was frequent in pediatric acute myeloid leukemia patients with t(8;21) in Japan: a study of the Japanese childhood AML cooperative study group.
- Published in:
- 2007
- By:
- Publication type:
- Letter
No nucleophosmin mutations in pediatric acute myeloid leukemia with normal karyotype: a study of the Japanese Childhood AML Cooperative Study Group.
- Published in:
- 2007
- By:
- Publication type:
- Letter