Zobrazeno 1 - 10
of 171
pro vyhledávání: '"D. Powars"'
Autor:
Nancy Bunin, FL Johnson, K Ohene-Frempong, C Lenarsky, Mark C. Walters, J.P. Vannier, D Powars, Keith M. Sullivan, F Bernaudin, G Souillet
Publikováno v:
Blood. 85:879-884
Seven of 21 patients with sickle cell anemia developed neurologic complications 5 to 243 days (median, 33 days) after allogeneic marrow transplantation. Among these 7 patients, indications for transplantation included either a past history of stroke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c4fc8448b454f989bf128e5be4f8d01
https://doi.org/10.1182/blood.v85.4.879.bloodjournal854879
https://doi.org/10.1182/blood.v85.4.879.bloodjournal854879
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:
K.G. Miller, C. Liu, J.V. Browning, S.F. Pekar, P.J. Sugarman, M.C. Van Fossen, L. Mullikin, D. Queen, M.D. Feigenson, M.-P. Aubry, L.D. Burckle, D. Powars, T. Heibel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6920d7602826df37c2ea731d6129da0
https://doi.org/10.2973/odp.proc.ir.150xs.041.1996
https://doi.org/10.2973/odp.proc.ir.150xs.041.1996
Autor:
M C, Walters, K M, Sullivan, F, Bernaudin, G, Souillet, J P, Vannier, F L, Johnson, C, Lenarsky, D, Powars, N, Bunin, K, Ohene-Frempong
Publikováno v:
Blood. 85(4)
Seven of 21 patients with sickle cell anemia developed neurologic complications 5 to 243 days (median, 33 days) after allogeneic marrow transplantation. Among these 7 patients, indications for transplantation included either a past history of stroke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::571cc3d9f58cf4c3dd3a07d6ff30162b
https://pubmed.ncbi.nlm.nih.gov/7795250
https://pubmed.ncbi.nlm.nih.gov/7795250
Publikováno v:
Seminars in hematology. 27(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec2a786a05773407bc153aea636026fc
https://pubmed.ncbi.nlm.nih.gov/2255920
https://pubmed.ncbi.nlm.nih.gov/2255920
Publikováno v:
Journal of the Association for Academic Minority Physicians : the official publication of the Association for Academic Minority Physicians. 1(3)
Clinical and necropsy findings in 11 patients with sickle cell anemia (SS) indicate that intracranial hemorrhage (IH) is a delayed sequela of the same vasculopathy that causes cerebral infarction during childhood. Evidence of prior cerebral infarctio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::53ca12a76f1e2e61d022ed101755bc84
https://pubmed.ncbi.nlm.nih.gov/2136621
https://pubmed.ncbi.nlm.nih.gov/2136621
Publikováno v:
Blood. 50:647-655
Glutathione peroxidase (GSHPx) activity was found to be greatly elevated in members of a family with alpha-thalassemia. Eleven other families with proven alpha-thalassemia were investigated, and all but one subject with hemoglobin H disease had incre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11cc463e0a3b5a8588aa13d1e885b057
https://doi.org/10.1182/blood.v50.4.647.bloodjournal504647
https://doi.org/10.1182/blood.v50.4.647.bloodjournal504647
Autor:
D. Powars
Publikováno v:
JAMA: The Journal of the American Medical Association. 245:1839-1842
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d2ac4bd28c1c42ee46e038ade01c82f
https://doi.org/10.1001/jama.245.18.1839
https://doi.org/10.1001/jama.245.18.1839
Publikováno v:
Journal of Chronic Diseases. 35:401-409
A modified life table procedure is introduced designed to study the survival of patients with congenital genetic disorders with the endpoint defined by a complication or death. It uses the ages of the patients as the time axis as in "population' or "
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b56ec550e4e74eb7a2c9ab7c7ee00766
https://doi.org/10.1016/0021-9681(82)90010-8
https://doi.org/10.1016/0021-9681(82)90010-8
Autor:
AM Levine, P Thornton, SJ Forman, P Van Hale, D Holdorf, CL Rouault, D Powars, DI Feinstein, RJ Lukes
Publikováno v:
Blood. 55:607-611
To clarify the clinicopathologic characteristics of Coombs' positivity in Hodgkin's disease, the records of 71 cases were reviewed. The direct Coombs test was positive in seven. Mean age of the seven was 22 yr (range 11–33). All were males. All had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4607a0c1bc7156437a7552cf6ab0f327
https://doi.org/10.1182/blood.v55.4.607.607
https://doi.org/10.1182/blood.v55.4.607.607