Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nikisha S. Khare"'
Publikováno v:
Canadian Journal of Latin American and Caribbean Studies / Revue canadienne des études latino-américaines et caraïbes. :1-27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9d5c331ad66f77bde3772b1615b6def
https://doi.org/10.1080/08263663.2023.2193045
https://doi.org/10.1080/08263663.2023.2193045
Autor:
Steven Pi, Adam Bryant, Alok P. Vakil, Yasser Abou Mourad, Jason Pal, Soo Yeon Lee, Areej Al Mugairi, Sally C Lau, Nikisha S. Khare, Bakul I. Dalal
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 14:239-244
The standard-risk (SR) subgroup of acute lymphoblastic leukemia in adults (aALL) is a heterogeneous category, with a 20% to 40% relapse rate and a wide range of relapse-free survival (RFS) and overall survival (OS). There is a need to identify at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::526577affbf10a83f46ad5598180c983
https://doi.org/10.1016/j.clml.2013.10.003
https://doi.org/10.1016/j.clml.2013.10.003
Autor:
Bakul I Dalal, Steven Pi, Alok P. Vakil, Jason Pal, Adam Bryant, Soo Yeon Lee, Areej Al Mugairi, Yasser Abou Mourad, Nikisha S. Khare, Sally C Lau
Publikováno v:
Journal of Leukemia.
Background: In adult patients with T–cell acute lymphoblastic leukemia (T–aALL), age, WBC count and cytogenetics are used for prognostic stratification. We report the prognostic significance of immunophenotype in T– aALL patients. Methods: We a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1da13a79a257a3ca8ef7cd228600c784
https://doi.org/10.4172/2329-6917.1000172
https://doi.org/10.4172/2329-6917.1000172
Autor:
Nikisha S. Khare, Sophie Yu Wang, Mikhyla J. Richards, Luke Y.C. Chen, Bakul I. Dalal, Alok P. Vakil
Publikováno v:
Annals of hematology. 94(7)
Hemophagocytic lymphohistiocytosis (HLH) is a final common pathway resulting from diverse immune processes. Most of the current understanding of HLH is based on studies involving pediatric patients (pHLH). Adult HLH (aHLH) is distinct from pHLH, with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4fb02252e5118270e5a0a6520a0a1f5
https://pubmed.ncbi.nlm.nih.gov/25800135
https://pubmed.ncbi.nlm.nih.gov/25800135
Autor:
Bakul I. Dalal, Nikisha S. Khare
Publikováno v:
Cytometry. Part B, Clinical cytometry. 84(1)
Background: Paroxysmal nocturnal hemoglobinuria (PNH) is diagnosed by documenting partial or complete absence of glycosyl phosphatidyl inositol (GPI)-associated ligands in neutrophils, monocytes, and red blood cells (RBCs). The monocytes can be separ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92b2f2f5527ae5e7c224acef7de722e3
https://pubmed.ncbi.nlm.nih.gov/23018985
https://pubmed.ncbi.nlm.nih.gov/23018985
Publikováno v:
Blood. 120:3267-3267
3267 Background: Adult hemophagocytic lymphohistiocytosis (aHLH) is a rare, aggressive, often lethal disease presenting with cytopenias and infections. By contrast, pediatric HLH is a relatively homogeneous, familial condition, with 75% response rate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f99f3f705bd5ac3a8ae0bad7bf72fb7d
https://doi.org/10.1182/blood.v120.21.3267.3267
https://doi.org/10.1182/blood.v120.21.3267.3267
Autor:
Steven Pi, Bakul I. Dalal, Nikisha S. Khare, Adam Bryant, Jason Pal, Areej Al Mugairi, Sally C Lau, Yasser Abou Mourad
Publikováno v:
Biology of Blood and Marrow Transplantation. (2):S223-S224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7283f47c4d3aff03ce17df01b89f5bdc