Zobrazeno 1 - 10
of 10
pro vyhledávání: '"S E Schiff"'
Autor:
M L Markert, D D Kostyu, F E Ward, T M McLaughlin, T J Watson, R H Buckley, S E Schiff, R M Ungerleider, J W Gaynor, K T Oldham, S M Mahaffey, M Ballow, D A Driscoll, L P Hale, B F Haynes
Publikováno v:
The Journal of Immunology. 158:998-1005
Transplantation of cultured postnatal human thymus was performed in a patient with complete DiGeorge syndrome. Biopsy of the graft 3 mo after implantation revealed normal CD1+ thymocytes in thymic cortical epithelial regions and CD1- thymocytes in th
Autor:
C M, Davis, T M, McLaughlin, T J, Watson, R H, Buckley, S E, Schiff, L P, Hale, B F, Haynes, M L, Markert
Publikováno v:
Journal of clinical immunology. 17(2)
Complete DiGeorge syndrome is an immunodeficiency disease characterized by thymic aplasia and the absence of functioning peripheral T cells. A patient with this syndrome was transplanted with cultured postnatal human thymic tissue. Within 5 weeks of
Autor:
M L, Markert, D D, Kostyu, F E, Ward, T M, McLaughlin, T J, Watson, R H, Buckley, S E, Schiff, R M, Ungerleider, J W, Gaynor, K T, Oldham, S M, Mahaffey, M, Ballow, D A, Driscoll, L P, Hale, B F, Haynes
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 158(2)
Transplantation of cultured postnatal human thymus was performed in a patient with complete DiGeorge syndrome. Biopsy of the graft 3 mo after implantation revealed normal CD1+ thymocytes in thymic cortical epithelial regions and CD1- thymocytes in th
Autor:
R H, Buckley, S E, Schiff, R I, Schiff, J L, Roberts, M L, Markert, W, Peters, L W, Williams, F E, Ward
Publikováno v:
Seminars in hematology. 30(4 Suppl 4)
From May 1992 to March 1993, 50 infants with severe combined immunodeficiency (SCID) were given bone marrow transplants at Duke University Medical Center. None received chemotherapy for conditioning or for graft-versus-host disease (GVHD) prophylaxis
Using serum creatinine concentrations to screen for inappropriate dosage of renally eliminated drugs
Publikováno v:
American journal of hospital pharmacy. 48(9)
The impact on drug therapy and costs of a program to identify and correct unadjusted dosage in renally impaired patients is described. The program was instituted in May 1988 by the clinical pharmacy staff at a 272-bed hospital. Each day the clinical
Autor:
R H Buckley, S E Schiff, H A Sampson, R I Schiff, M L Markert, A P Knutsen, M S Hershfield, A T Huang, G H Mickey, F E Ward
Publikováno v:
The Journal of Immunology. 136:2398-2407
Recent advances in the prevention of graft-vs-host disease (GVHD) have allowed the use of haploidentical bone marrow cells for correction of lethal genetic defects of the immune system. Sequential analyses of blood lymphocyte phenotypes and functions
Publikováno v:
Clinical and experimental immunology. 72(1)
Transplacentally acquired lymphoid chimerism was detected in two infants with severe combined immunodeficiency (SCID) by two-colour cytofluorographic studies. These cells had no demonstrable function in studies in vitro. Following T cell-depleted mat
Autor:
S E, Schiff, R H, Buckley
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 138(7)
After administration of haploidentical stem cells to infants with severe combined immunodeficiency disease (SCID), mature T cells of donor karyotype appear later in the recipient without causing graft-vs-host disease (GVHD). To investigate the effect
Publikováno v:
Clinical and experimental immunology. 68(3)
Morphological, phenotypic and functional analyses were made of cells obtained at each step after successive treatments of 23 separate human bone marrow suspensions with soybean lectin and sheep erythrocytes (SRBC). The average total number of nucleat
Autor:
R H, Buckley, S E, Schiff, H A, Sampson, R I, Schiff, M L, Markert, A P, Knutsen, M S, Hershfield, A T, Huang, G H, Mickey, F E, Ward
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 136(7)
Recent advances in the prevention of graft-vs-host disease (GVHD) have allowed the use of haploidentical bone marrow cells for correction of lethal genetic defects of the immune system. Sequential analyses of blood lymphocyte phenotypes and functions