Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Vishwas S. Sakhalkar"'
Autor:
Jatayah N Sheed, William T Uphouse, Francis C Dane, Om V Sakhalkar, Vishwas S Sakhalkar, Olga N. Uchakina, Peter N. Uchakin
Publikováno v:
Journal of Hematology
Background: Immunomodulatory effects of macrolides in chronic inflammation are well known. In this study, we tested our hypothesis that azithromycin (AZT) can decrease inflammation in pediatric patients with sickle cell disease (SCD). Methods: The us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa1326cc10da282b4e3b6936b54c8a5
https://doi.org/10.14740/jh827
https://doi.org/10.14740/jh827
Autor:
G. C. Caldito, J. D. Cotelingam, Vishwas S. Sakhalkar, Linda M. Hawthorne, Diana M Veillon, K. Roberts, McCaskill D
Publikováno v:
Annals of the New York Academy of Sciences. 1054:495-499
Extended antigen (C, E, K) matching decreased the incidence of alloantibody (alloAB) and autoantibody (autoAB) formation, in addition to eliminating transfusion reactions in the multiply transfused sickle cell disease patients. AlloAB formation possi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76866781518413f2b4e4d72970c1e4d3
https://doi.org/10.1196/annals.1345.072
https://doi.org/10.1196/annals.1345.072
Autor:
Diana M Veillon, Mary L. Nordberg, James D. Cotelingam, Rachel B Flamholz, Majed Jeroudi, Vishwas S. Sakhalkar
Publikováno v:
Laboratory Medicine. 35:404-407
case study [hematology | cytology | immunology] Myeloblastic Proliferation in the Peripheral Blood of a Neonate With Down Syndrome Rachel B. Flamholz, MD,1 Diana M. Veillon, MD,1 Majed Jeroudi, MD,2 Vishwas S. Sakhalkar, MD,2 Mary L. Nordberg, PhD,1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a849da7621d86f923d6f784419e1acd8
https://doi.org/10.1309/tdjq1kw8yjn5w2qj
https://doi.org/10.1309/tdjq1kw8yjn5w2qj
Publikováno v:
American Journal of Hematology. 76:57-60
Vascular cell adhesion molecule-1 (VCAM-1) has been implicated as being important in the pathophysiology of acute pain episodes (APE) and acute chest syndrome (ACS) of sickle cell disease (SCD). The frequency of these episodes is reduced by chronic t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cd3142fce303aceac735701166cec0a
https://doi.org/10.1002/ajh.20016
https://doi.org/10.1002/ajh.20016
Introduction Among the early successes of allogeneic BMT were those achieved in the area of congenital immunodeficiencies. In certain diseases and certain donor–recipient combinations, over 90% of patients can be cured by allogeneic transplantation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f76e29f1bde673f52957a0b4374f81be
https://doi.org/10.1017/cbo9780511575525.018
https://doi.org/10.1017/cbo9780511575525.018
Autor:
Reinhold Munker, Vishwas S. Sakhalkar
Publikováno v:
Contemporary Hematology ISBN: 9781588295576
Acute lymphoblastic leukemias (ALLs) are a group of hematological neoplasias defined by cytomorphology, cytochemistry, immunological markers, and more recently, molecular markers. The prognosis of ALL has much improved in the last 30 yr, especially i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6b6a610d91e2c9e77274312c3a4fc28
https://doi.org/10.1007/978-1-59745-149-9_10
https://doi.org/10.1007/978-1-59745-149-9_10
Autor:
Reinhold Munker, Vishwas S. Sakhalkar
Publikováno v:
Contemporary Hematology ISBN: 9781588295576
The development of the immune system and its function are outlined in Chapter 1. Congenital immunodeficiencies are rare; more details can be found in pediatric textbooks. Here, only the most important entities are discussed. Acquired immunodeficienci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7df0b87c55d757646a45bef5d385d52a
https://doi.org/10.1007/978-1-59745-149-9_17
https://doi.org/10.1007/978-1-59745-149-9_17
Publikováno v:
Journal of pediatric hematology/oncology. 23(9)
Persistent fever with pancytopenia and hepatomegaly with negative blood cultures and no obvious focus of infection in a child with Down syndrome should arouse a suspicion of leukemia. Bone marrow examination and clot biopsy from one such patient reve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07e982d4c3eb5bd5038d3d411ffad108
https://pubmed.ncbi.nlm.nih.gov/11902310
https://pubmed.ncbi.nlm.nih.gov/11902310
Publikováno v:
Blood. 120:2091-2091
Abstract 2091 Background: Patients with sickle cell trait (AS) are generally asymptomatic, but they are known to be at risk of developing acute morbidity such as splenic infarction mainly occurring on exposure to high altitude. Much lesser known to m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d53e057ef1e1878c89867b64c526e807
https://doi.org/10.1182/blood.v120.21.2091.2091
https://doi.org/10.1182/blood.v120.21.2091.2091
Autor:
Vishwas S. Sakhalkar, James D. Cotelingam, Deborah M. McCaskill, Gloria Caldito, Linda M. Hawthorne, Diana M Veillon
Publikováno v:
Blood. 106:946-946
Aim: To study transfusion reactions in our SCD patients before and after instituting the practice of transfusing C, E, K blood type negative (CEKneg) packed red blood cell (pRBC) units. Material and Methods: We retrospectively reviewed blood bank rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0a1405b60ac853008edef45963c772a
https://doi.org/10.1182/blood.v106.11.946.946
https://doi.org/10.1182/blood.v106.11.946.946