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Journal of Pharmaceutical Sciences|June 1, 1992
Pharmacokinetic model for subcutaneous absorption of cyclosporine in the rabbit during chronic treatmentA K Shah, R C Brundage, A Gratwohl, et al.
British Journal of Haematology|August 1, 1989
Complete recovery of marrow function after treatment with anti-lymphocyte globulin is associated with high, whereas early failure and development of paroxysmal nocturnal haemoglobinuria are associated with low endogenous G-CSA-releaseC Nissen, Y Moser, V dalle Carbonare, et al.
Blut|April 1, 1986
The release of interleukin-2 (IL-2) and colony stimulating activity (CSA) in aplastic anemia patients: opposite behaviour with improvement of bone marrow functionC Nissen, Y Moser, J Weis, et al.
Schweizerische Medizinische Wochenschrift|January 16, 1988
[A Candida krusei epidemic in a hematology department]C Berger, R Frei, A Gratwohl, et al.
British Journal of Haematology|October 1, 1986
Acquired aplastic anaemia: a PNH-like disease?C Nissen, A Gratwohl, B Speck, et al.
Transplantation|June 9, 1999
Sequencing of two HLA-A blank alleles: implications in unrelated bone marrow donor matchingR Zanone-Ramseier, A Gratwohl, J Gmür, et al.
Experimental Hematology|December 1, 1990
High-dose recombinant human erythropoietin for treatment of anemia in myelodysplastic syndromes and paroxysmal nocturnal hemoglobinuria: a pilot studyC Stebler, A Tichelli, H Dazzi, et al.
Bone Marrow Transplantation|August 17, 2010
Graft source determines human hematopoietic progenitor distribution pattern within the CD34(+) compartmentC Arber, J Halter, M Stern, et al.
Journal of Pediatric Hematology/Oncology|November 1, 1995
Boys but not girls with T-lineage acute lymphocytic leukemia (ALL) are different from children with B-progenitor ALL. Population-based data results of initial prognostic factors and long-term event-free survival. Swiss Pediatric Oncology GroupP Imbach, A Fuchs, W Berchtold, et al.
Gut|June 1, 1992
Occurrence of large granular lymphocytes and natural killer cells in the epithelium of the gut distinguishes two different coeliac diseasesF Hadziselimovic, L R Emmons, U Schaub, et al.
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