Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Virgil McKie"'
Autor:
Paul J. Nietert, Miguel R. Abboud, Deborah Disco, Lina B. Karam, Susan S. Baker, Joseph Laver, David N. Lewin, Robert D. Baker, Sherron M. Jackson, Virgil McKie
Publikováno v:
Pediatric Blood & Cancer. 50:62-65
Chronic transfusions are effective in preventing stroke and other complications of sickle cell disease. The aim of this study was to determine whether serum ferritin levels correlated with liver iron content in sickle cell patients on chronic transfu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::613156c6056b53e20963ce139d0ca49c
https://doi.org/10.1002/pbc.21215
https://doi.org/10.1002/pbc.21215
Autor:
Stephen H. Embury, Louis J. Elsas, Charles H. Pegelow, Abdullah Kutlar, Winfred C. Wang, Scott T. Miller, Elizabeth C. Wright, Catherine Driscoll, Virgil McKie, Lewis L. Hsu, Gerald M. Woods, Robert J. Adams, Anne Hurlet
Publikováno v:
Journal of Pediatric Hematology/Oncology. 25:622-628
Cerebrovascular complications of sickle cell disease (SCD) are common, but the risk factors remain unclear. The multicenter Stroke Prevention Trial in Sickle Cell Anemia (STOP) provided an opportunity to examine alpha thalassemia-2 as a modifying ris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::568bba39ede2ddf8eed593a552831642
https://doi.org/10.1097/00043426-200308000-00007
https://doi.org/10.1097/00043426-200308000-00007
Autor:
Charles H. Pegelow, Lori Styles, Donald Brambilla, Anne Hurlet, Brian Berman, Kantilal Patel, M. Catherine Driscoll, Virgil McKie, Beatrice Files, Nancy F. Olivieri, Richard A. Drachtman
Publikováno v:
Blood. 101:2401-2404
Cerebrovascular disease is a common cause of morbidity in sickle cell anemia (HbSS): approximately 10% of patients have a clinical stroke before 20 years of age, and another 22% have silent infarction on magnetic resonance imaging. The phenotypic var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58769fbc0e3f9eb1292755e0a6dcd357
https://doi.org/10.1182/blood.v101.6.2401
https://doi.org/10.1182/blood.v101.6.2401
Publikováno v:
Journal of Pediatric Hematology/Oncology. 24:585-588
Stroke is the most common neurologic complication of sickle cell disease. Acute chest syndrome (ACS) is a known risk factor for stroke in this population. Two patients (a 12-year-old boy and a 6-year-old girl) developed acute change of mental status
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e106dbf4fd0d102907851a7fa6d7ff
https://doi.org/10.1097/00043426-200210000-00021
https://doi.org/10.1097/00043426-200210000-00021
Autor:
Elliott P. Vichinsky, Lynne D. Neumayr, Ann N. Earles, Roger Williams, Evelyne T. Lennette, Deborah Dean, Bruce Nickerson, Eugene Orringer, Virgil McKie, Rita Bellevue, Charles Daeschner, Miguel Abboud, Mark Moncino, Samir Ballas, Russell Ware, Elizabeth A. Manci
Publikováno v:
New England Journal of Medicine. 342:1855-1865
Background 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 emb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f79b6c49ecd104fa1a5d85404bf80c9e
https://doi.org/10.1056/nejm200006223422502
https://doi.org/10.1056/nejm200006223422502
Autor:
Gerald M. Woods, Charles H. Pegelow, Virgil McKie, Miguel R. Abboud, Robert A. Zimmerman, Nancy F. Olivieri, Abdullah Kutlar, Charles D. Scher, Scott T. Miller, Brian Berman, Elizabeth C. Wright, Myron A. Waclawiw, Duane Bonds, E. S. Roach, Dianne Gallagher, Catherine Driscoll, Winfred C. Wang, Beatrice Files, Fenwick T. Nichols, Donald Brambilla, Elizabeth Carl, Lewis L. Hsu, Robert J. Adams, Anne Hurlet, E. Vichinsky
Publikováno v:
New England Journal of Medicine. 339:1478-1481
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::385a2fdf8fa853bca5b45e164db6faf9
https://doi.org/10.1056/nejm199811123392014
https://doi.org/10.1056/nejm199811123392014
Autor:
J. B. Wilson, Ferdane Kutlar, Anne Marie McMorrow Tuohy, Hernan Sabio, Virgil McKie, Abdullah Kutlar
Publikováno v:
Journal of Pediatric Hematology/Oncology. 20:570-573
Purpose To present the occurrence of Hb Hammersmith as a de novo mutation in African-American twins with multiple congenital anomalies. Methods Standard hematologic methods were used. The presence of an unstable Hb variant was confirmed by brilliant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1c4aa1e85b0233fc5a99bc1401fc8cf
https://doi.org/10.1097/00043426-199811000-00013
https://doi.org/10.1097/00043426-199811000-00013
Publikováno v:
Journal of Pediatric Hematology/Oncology. 19:455-458
PURPOSE: The purpose of this report is to describe the clinical and pathologic features of a patient with acute thrombosis of both internal carotid arteries leading to death. METHODS: This is a case report of special interest because of extensive bra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2a9b0ef251d21877cb3af4d4b0a86f3
https://doi.org/10.1097/00043426-199709000-00009
https://doi.org/10.1097/00043426-199709000-00009
Autor:
Abdullah Kutlar, Virgil McKie, Stephen H. Embury, Henry A. Erlich, Pranee Sutcharitchan, Titus H.J. Huisman, R. Saiki
Publikováno v:
Blood. 86:1580-1585
DNA-based diagnosis of the beta thalassemias provides accuracy to newborn screening genetic counseling, and prenatal diagnosis. However, the use of polymerase chain reaction (PCR)-based methods is challenged by the great number of different-beta-thal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcbb3542dd3b8694f9a258f9a27bb90f
https://doi.org/10.1182/blood.v86.4.1580.bloodjournal8641580
https://doi.org/10.1182/blood.v86.4.1580.bloodjournal8641580
Autor:
Charles H. Pegelow, Miguel R. Abboud, Donald Brambilla, Winfred C. Wang, Brian Berman, Robert J. Adams, Scott T. Miller, Nancy F. Olivieri, Elliott Vichinsky, Virgil McKie
Publikováno v:
The Journal of Pediatrics. 126:896-899
Objective: To determine the effect of a transfusion program on risk of stroke recurrence in children with sickle cell disease. Design: The clinical course and experience with transfusion therapy at eight centers were reviewed for subjects whose initi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8853b602df74de874faf99a87fa4a2b
https://doi.org/10.1016/s0022-3476(95)70204-0
https://doi.org/10.1016/s0022-3476(95)70204-0