Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Roger S. Riley"'
Publikováno v:
Journal of Pathology Informatics, Vol 12, Iss 1, Pp 23-23 (2021)
Objectives: Bone marrow evaluation plays a critical role in the diagnosis, staging, and monitoring of many diseases. Although there are standardized guidelines for assessing bone marrow specimen quality, there is a lack of evidence-based tools to per
Externí odkaz:
https://doaj.org/article/cd4d49629c9b40698430924f0f1d777c
Publikováno v:
Experimental and Clinical Transplantation. 17:111-114
Posttransplant lymphoproliferative disorder is a serious complication of solid-organ transplant. Extranodal involvement is common; however, isolated involvement of the central nervous system is extremely rare and represents a particularly difficult t
Publikováno v:
Journal of Pathology Informatics
Journal of Pathology Informatics, Vol 12, Iss 1, Pp 23-23 (2021)
Journal of Pathology Informatics, Vol 12, Iss 1, Pp 23-23 (2021)
Objectives: Bone marrow evaluation plays a critical role in the diagnosis, staging, and monitoring of many diseases. Although there are standardized guidelines for assessing bone marrow specimen quality, there is a lack of evidence-based tools to per
Publikováno v:
Neuromethods ISBN: 9781071604267
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3296848da6fe58bba3b1d043b93ab374
https://doi.org/10.1007/978-1-0716-0428-1_14
https://doi.org/10.1007/978-1-0716-0428-1_14
Publikováno v:
American Journal of Clinical Pathology. 156:S104-S104
Introduction/Objective Microdeletion of a region of the short arm of chromosome 19 results in a very rare syndrome called 19p13.3 deletion syndrome, which manifest itself in developmental delay as well as structural abnormalities such as facial dysmo
Publikováno v:
Laboratory medicine. 50(4)
Storage pool deficiency (SPD) is a group of rare platelet disorders that result from deficiencies in α-granules, δ-granules, or both. One type of α-SPD is gray platelet syndrome (GPS), caused by mutations in the neurobeachin-like 2 (NBEAL2) gene t
Publikováno v:
American Journal of Clinical Pathology. 145:277-281
Objectives: To present a unique case where detection of oligoclonal bands in serum led to the diagnosis of human immunodeficiency virus (HIV) infection. Methods: A 64-year-old man treated for hypertension for 11 years had laboratory tests ordered by
Publikováno v:
Blood Cancer Discovery. 1:PO-52
Background: Richter syndrome (RS) is defined as the transformation of chronic lymphocytic leukemia (CLL) into an aggressive lymphoma, most often diffuse large B-cell lymphoma (DLBCL). It carries a poor prognosis and is often unresponsive to conventio
Publikováno v:
Laboratory medicine. 47(2)
D-dimers are formed by the breakdown of fibrinogen and fibrin during fibrinolysis. D-dimer analysis is critical for the diagnosis of deep vein thrombosis, pulmonary embolism, and disseminated intravascular coagulation. Modern assays for D-dimer are m
Autor:
Robert A. Fisher, James J. Stone, Ramazan Eryilmaz, Dawen Bu, Seong-Hwan Chang, Davis Massey, Roger S. Riley, Hwon-Kyum Park
Publikováno v:
Journal of Surgical Research. 128:50-54
Background Isografts are used as controls in many transplant experiments. Our laboratory and others have noticed histological changes in control isograft groups of rats similar to allograft groups, suggesting alloantigen-independent factors contribut