Zobrazeno 1 - 10
of 66
pro vyhledávání: '"R Bellevue"'
Autor:
J. H. Bailey, Abdullah Kutlar, N. Talischy-Zahed, Elliott Perlin, Wendell F. Rosse, D. Temple, Josef T. Prchal, Martin H. Steinberg, George Phillips, Charles H. Pegelow, R. Bellevue, A. Davis, T. Moeller, Kenneth Bridges, P. Ryans, G. Tirado, A. Brenner, D. Davies, M. McGee, G. Ramirez, Eugene P. Orringer, E. Case, L. Waller, J. Ullrich, V. Knors, D. Gardner, A. Platt, T. Nagle, Mabel Koshy, K. McLaughlin, J. Gibson, S. Childerie, A. Anderson, T. McArdle, C. Ewart, Stephen H. Embury, E. Wilkes, P. Di Paolo, G. E. Allen, C. Lent, B. Maddox, S. Eckert, S. Gargiulo, Brian W. Berman, S. K. Ballas, L. Fishpaw, James R. Eckman, R. O'Brien, Susan Jones, Michael L. Terrin, M. Bergner, G. Pendarvis, Wally R. Smith, C. Winograd, A. Earles, K. Kleman, J. Moshang, K. Williams, J. Braddock, Harvey Dosik, Oswaldo Castro, E. M. Rodriguez, B. Tynan, A. Schmotzer, George J. Dover, Margaret Telfer, Helga Finke, Samuel Charache, S. Hernandez, Nancy F. Olivieri, K. Chiarucci, Timothy M. Carlos, Elliott Vichinsky, N. Lewis, L. Dorn, L. Keverline, Paul Swerdlow, Franca B. Barton, Richard D. Moore, A. Tracy, K. Genther, B. Scott, B. Schmidt, V. Sabahi, D. Strayhorn, Samir K. Ballas, Paul F. Milner, H. Souffrant, M. Sheikhai, D. Shaw, D. Peace, S. Claster, Susan B. Shurin, R. Harrell, J. Siteman, A. Johnson-Telfair, P. Gascon, L. Usry, P. Luthra
Publikováno v:
American Journal of Hematology. 64:26-31
The Multicenter Study of Hydroxyurea in Sickle Cell Anemia (MSH) demonstrated the efficacy of hydroxyurea in reducing the rate of painful crises compared to placebo. We used resource utilization data collected in the MSH to determine the cost-effecti
Autor:
E P, Vichinsky, L D, Neumayr, A N, Earles, R, Williams, E T, Lennette, D, Dean, B, Nickerson, E, Orringer, V, McKie, R, Bellevue, C, Daeschner, E A, Manci
Publikováno v:
The New England journal of medicine. 342(25)
The acute chest syndrome is the leading cause of death among patients with sickle cell disease. Since its cause is largely unknown, therapy is supportive. Pilot studies with improved diagnostic techniques suggest that infection and fat embolism are u
Autor:
L, Neumayr, M, Koshy, C, Haberkern, A N, Earles, R, Bellevue, K, Hassell, S, Miller, D, Black, E, Vichinsky
Publikováno v:
American journal of hematology. 57(2)
While surgery is commonly required for complications related to hemoglobin SC (HbSC) disease, little is known about the perioperative complications or the indications for preoperative transfusion in this group. We describe the patient characteristics
Publikováno v:
The American journal of gastroenterology. 91(6)
To determine the prevalence of hepatitis C virus (HCV) antibody in patients with sickle cell disease and to analyze the nature of chronic liver disease in these patients.A total of 99 patients attending a comprehensive sickle cell and thalassemia pro
Autor:
F M, Gill, L A, Sleeper, S J, Weiner, A K, Brown, R, Bellevue, R, Grover, C H, Pegelow, E, Vichinsky
Publikováno v:
Blood. 86(2)
Within the Cooperative Study of Sickle Cell Disease, 694 infants with confirmed sickle cell disease were enrolled at less than 6 months of age. Information about the nature and frequency of complications was collected prospectively over a 10-year per
Autor:
P F, Milner, A P, Kraus, J I, Sebes, L A, Sleeper, K A, Dukes, S H, Embury, R, Bellevue, M, Koshy, J W, Moohr, J, Smith
Publikováno v:
Clinical orthopaedics and related research. (289)
The prevalence and incidence of osteonecrosis (ON) of the humeral head in sickle cell disease was determined by a study of 2524 patients who were entered into a prospective study and followed for an average of 5.6 years. At entry, 5.6% had roentgenog
Autor:
R. Bellevue, R. Ware, P. Waldron, P. Groncy, S. Robertson, C. Daeschner, E. Vichinsky, Lynne Neumayr, H.A. Hume, A. Wen, I. Browning, A. Earles, Miguel R. Abboud, R. Iyer, Claudia R. Morris, M. Moncino, E. Orringer, S. Ballas, P. Swerdlow, L. McMahon
Publikováno v:
Blood. 106:315-315
Acute Chest Syndrome (ACS) remains the leading cause of death and hospitalization in patients (pts) with sickle cell disease (SCD). There is limited data on the effects of ACS on lung function. From 1993 to 1997, 30 centers participated in the NACSG
Publikováno v:
Hemoglobin. 6:99-114
Utilizing restriction endonuclease mapping and molecular hybridization we have determined the number and arrangement of the alpha-globin genes in members of an American Black family in which alpha-thalassemia is present. In addition to chromosomes be
Autor:
A Smith, C L Sprung, Thomas Manis, Rao Tk, D M Holden, Richard D. Levere, R Bellevue, Eli A. Friedman, Khalid M. H. Butt
Publikováno v:
New England Journal of Medicine. 291:431-435
Renal failure, which developed in two patients with sickle-cell anemia, was treated by maintenance hemodialysis for six and seven months. Medullary cystic disease appeared to cause the uremia in a 32-year-old black man with sickle-cell anemia; in the
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