Zobrazeno 1 - 10
of 33
pro vyhledávání: '"W C, Mentzer"'
Autor:
M C, Walters, R, Storb, M, Patience, W, Leisenring, T, Taylor, J E, Sanders, G E, Buchanan, Z R, Rogers, P, Dinndorf, S C, Davies, I A, Roberts, R, Dickerhoff, A M, Yeager, L, Hsu, J, Kurtzberg, K, Ohene-Frempong, N, Bunin, F, Bernaudin, W Y, Wong, J P, Scott, D, Margolis, E, Vichinsky, D A, Wall, A S, Wayne, C, Pegelow, R, Redding-Lallinger, J, Wiley, M, Klemperer, W C, Mentzer, F O, Smith, K M, Sullivan
Publikováno v:
Blood. 95(6)
Fifty children who had symptomatic sickle cell disease received matched sibling marrow allografts between September 1991 and March 1999, with Kaplan-Meier probabilities of survival and event-free survival of 94% and 84%, respectively. Twenty-six pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b354f466994cdb08de58f1da39b0b376
https://pubmed.ncbi.nlm.nih.gov/10706855
https://pubmed.ncbi.nlm.nih.gov/10706855
Autor:
M C, Walters, M, Patience, W, Leisenring, Z R, Rogers, P, Dinndorf, S C, Davies, I A, Roberts, A, Yeager, J, Kurtzberg, N, Bunin, J P, Scott, D A, Wall, A S, Wayne, J, Wiley, P J, Darbyshire, W C, Mentzer, F O, Smith, K M, Sullivan
Publikováno v:
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 3(6)
We present updated results of a multicenter collaborative investigation of bone marrow transplantation for sickle cell disease. Between September 1991 and April 1997, thirty-four children less than 16 years of age with severe sickle cell disease rece
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0100d055a25eafd5d8293c383f9cfdd0
https://pubmed.ncbi.nlm.nih.gov/9502298
https://pubmed.ncbi.nlm.nih.gov/9502298
Autor:
M C, Walters, M, Patience, W, Leisenring, J R, Eckman, G R, Buchanan, Z R, Rogers, N E, Olivieri, E, Vichinsky, S C, Davies, W C, Mentzer, D, Powars, J P, Scott, F, Bernaudin, K, Ohene-Frempong, P J, Darbyshire, A, Wayne, I A, Roberts, P, Dinndorf, S, Brandalise, J E, Sanders, D C, Matthews, F R, Appelbaum, R, Storb, K M, Sullivan
Publikováno v:
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 2(2)
While allogeneic marrow transplantation is curative therapy for patients with sickle cell anemia, only a small fraction of patients in the United States receive this treatment. We surveyed participants in our multicenter study of marrow transplantati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0dbf58a0d1decdfebcec7e1845611b2b
https://pubmed.ncbi.nlm.nih.gov/9118298
https://pubmed.ncbi.nlm.nih.gov/9118298
Autor:
W C, Mentzer, K, Matthay
Publikováno v:
Current opinion in pediatrics. 7(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::75f4ab5879c3acccd5bbf94192c00e19
https://pubmed.ncbi.nlm.nih.gov/7728200
https://pubmed.ncbi.nlm.nih.gov/7728200
Publikováno v:
The American journal of pediatric hematology/oncology. 16(1)
To determine who might qualify for allogeneic bone marrow transplantation (BMT), we reviewed the medical records of all 143 patients with sickle cell anemia under the age of 16 years who were registered at our center.A total of 135 records were compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e7380ebf98c749bf1dafb3f3edd3dd24
https://pubmed.ncbi.nlm.nih.gov/8311169
https://pubmed.ncbi.nlm.nih.gov/8311169
Publikováno v:
The American journal of pediatric hematology/oncology. 16(1)
As of June 1992, five patients with sickle cell disease had been treated by matched sibling bone marrow transplantation in the United States.Three patients underwent transplantations for complications related to sickle cell disease, two with previous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b673e8dd71fe118f4d97cc9b5de2794c
https://pubmed.ncbi.nlm.nih.gov/8311168
https://pubmed.ncbi.nlm.nih.gov/8311168
Publikováno v:
The Journal of biological chemistry. 266(27)
A 31-kDa human erythrocyte integral protein, band 7.2b, has been purified to better than 95% homogeneity. The polypeptide was found to be insoluble in most detergents and was isolated in denatured form by gel filtration in the presence of sodium dode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a6d389c0ba9d2944e9d4c9bd4aec5d50
https://pubmed.ncbi.nlm.nih.gov/1655727
https://pubmed.ncbi.nlm.nih.gov/1655727
Publikováno v:
Contributions to nephrology. 88
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aabb17cc0902a82cf01160effbc21de7
https://pubmed.ncbi.nlm.nih.gov/2040193
https://pubmed.ncbi.nlm.nih.gov/2040193
Publikováno v:
Journal of Supramolecular Structure. 9:275-288
The marked increase in cation (Na+, K+) permeability that results in swollen, cup-shaped red cells in the hereditary stomatocytosis syndrome can be corrected in vitro with a bifunctional crosslinking reagent, dimethyl adipimidate (DMA). 45Ca influx i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34dda933cf1d004b9842d3b8b8e4c681
https://doi.org/10.1002/jss.400090212
https://doi.org/10.1002/jss.400090212
Autor:
Hal E. Nourse, W. C. Mentzer
Publikováno v:
Journal of the Aeronautical Sciences. 7:227-234
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4ca9feefe42b2192d29c0a729cbbffe
https://doi.org/10.2514/8.1103
https://doi.org/10.2514/8.1103