Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Levette N. Dunbar"'
Autor:
Martin L. Blakely, Henry E. Rice, Shawn D. St. Peter, Andrew D. Campbell, Saleem Islam, Levette N. Dunbar, Mary Brindle, Sanjeev Dutta, Mukta Sharma, Andrew M. Davidoff, Steve Bruch, C. Jason Smithers, Brad W. Warner, Rebeccah L. Brown, Jennifer A. Rothman, Theodosia A. Kalfa, Michaela Cada, Mary T. Austin, Audra Reiter, Bert Glader, Deborah Brown, Jacob C. Langer, Kerri Nottage, David B. Wilson, Brian R. Englum, Matthew M. Heeney, Fred Rescorla, Nicola A.M. Wright, Robert Fallon, Keith T. Oldham, Heather McDaniel, Bria J. Hall, J. Paul Scott
Publikováno v:
Pediatr Blood Cancer
BACKGROUND: Total splenectomy (TS) and partial splenectomy (PS) are used for children with congenital hemolytic anemia (CHA), although the long-term outcomes of these procedures are poorly defined. This report describes long-term outcomes of children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32ef764420ba1a49f911d7ec482ec099
https://europepmc.org/articles/PMC10151035/
https://europepmc.org/articles/PMC10151035/
Hematologic outcomes after total splenectomy and partial splenectomy for congenital hemolytic anemia
Autor:
Bertil Glader, Manjusha Kumar, Courtney D. Thornburg, Sanjeev Dutta, David B. Wilson, Michaela Cada, Fred Rescorla, Audra Reiter, Nicola A.M. Wright, Levette N. Dunbar, Shawn D. St. Peter, Saleem Islam, Steve Bruch, C. Jason Smithers, Keith T. Oldham, Martin L. Blakely, J. Paul Scott, Mary Brindle, Kathryn Q. Bernabe, Mary T. Austin, Theodosia A. Kalfa, Matthew M. Heeney, Shelley E. Crary, Melvin S. Dassinger, Jennifer A. Rothman, Andrew D. Campbell, Robert F. Sidonio, Jacob C. Langer, Kerri Nottage, Andrew M. Davidoff, Mukta Sharma, Brian R. Englum, Henry E. Rice, Rebeccah L. Brown, Sarah Leonard
Publikováno v:
Journal of Pediatric Surgery. 51:122-127
The purpose of this study was to define the hematologic response to total splenectomy (TS) or partial splenectomy (PS) in children with hereditary spherocytosis (HS) or sickle cell disease (SCD).The Splenectomy in Congenital Hemolytic Anemia (SICHA)
Autor:
Saleem Islam, Jacob C. Langer, Kerri Nottage, Henry E. Rice, Audra Reiter, Levette N. Dunbar, Mukta Sharma, Shawn D. St. Peter, Kathryn Q. Bernabe, Frederick J. Rescorla, Mary T. Austin, Courtney D. Thornburg, Rebeccah L. Brown, Brian R. Englum, Keith T. Oldham, Jennifer A. Rothman, Martin L. Blakely, Nicola A.M. Wright, Steve Bruch, Sarah Leonard, Mary Brindle, Michaela Cada, Manjusha Kumar, Andrew D. Campbell, Matthew M. Heeney, Theodosia A. Kalfa, Charles J. Smithers, Shelley E. Crary, Melvin S. Dassinger, Andrew M. Davidoff, Bertil Glader, David B. Wilson, Robert F. Sidonio, Sanjeev Dutta, J. Paul Scott
Publikováno v:
American Journal of Hematology. 90:187-192
The outcomes of children with congenital hemolytic anemia (CHA) undergoing total splenectomy (TS) or partial splenectomy (PS) remain unclear. In this study, we collected data from 100 children with CHA who underwent TS or PS from 2005–2013 at 16 si
Autor:
Levette N. Dunbar, Donna R. Rivera, LaRae Coleman Brown, Abraham G. Hartzema, Richard Lottenberg
Publikováno v:
ISRN Hematology
The purpose of this study was to characterize transfusion practices in the management of sickle cell disease and to identify factors attributing to differences in prescribing practices among Florida hematologists/oncologists. A cross-sectional study
Publikováno v:
Pediatric Blood & Cancer. 61:2118-2120
Autosomal dominant Beta Thalassemias are rare and are due to point or frame shift mutations resulting in production of abnormal unstable beta chains of hemoglobin which precipitate leading to hemolysis and anemia. We describe a case of Hemoglobin Hak
Publikováno v:
Pediatric bloodcancer. 61(11)
Autosomal dominant Beta Thalassemias are rare and are due to point or frame shift mutations resulting in production of abnormal unstable beta chains of hemoglobin which precipitate leading to hemolysis and anemia. We describe a case of Hemoglobin Hak
Autor:
Debbie Treise, Richard Lottenberg, Abraham G. Hartzema, Jane Ritho, Levette N. Dunbar, Jennifer M. LaVista
Publikováno v:
Journal of the National Medical Association. 101(3)
Background For the last decade, compelling evidence on hydroxyurea (HU) efficacy in certain adult patients with sickle cell disease (SCD) has supported recommendations for use of this drug to decrease morbidity and medical costs. Despite these benefi
Autor:
Levette N. Dunbar, Richard Lottenberg
Publikováno v:
The Hematologist. 3
Publikováno v:
Blood. 108:3342-3342
Limited data exist on Tx prescribing preferences in the management of SCD. To assess current Tx practices, we conducted a survey of Florida hematologists/oncologists from fall of 2005 through spring 2006. The 31-item survey addressed practice and SCD