Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Andrea, Illingworth"'
Publikováno v:
Cytometry Part B: Clinical Cytometry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d81a7ea96583bf1bfcad99f04fe9aee
https://doi.org/10.1002/cyto.b.22123
https://doi.org/10.1002/cyto.b.22123
Autor:
Pedro Horna, Ulrika Johansson, Katherina Psarra, Richard Torres, Sa A. Wang, Shuguang Huang, Julia Almeida, Kristy L. Wolniak, Fiona E. Craig, Andrea Illingworth
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Introducing a sensitive and specific peripheral blood flow cytometric assay for Sézary syndrome and mycosis fungoides (SS/MF) requires careful selection of assay design characteristics, and translation into a laboratory developed assay through devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aea0036b8a20b8d1584a529ebb98d824
https://doi.org/10.1002/cyto.b.21963
https://doi.org/10.1002/cyto.b.21963
Autor:
D. Robert Sutherland, Fernando Ortiz, Stephen J. Richards, Rakesh Nayyar, Miroslav Benko, Andrea Illingworth, Iuri Marinov
Publikováno v:
Cytometry Part B: Clinical Cytometry. 98:179-192
Background The diagnosis of paroxysmal nocturnal hemoglobinuria (PNH) relies on flow cytometric demonstration of loss of glycosyl-phosphatidyl inositol (GPI)-anchored proteins from red blood cells (RBC) and white blood cells (WBC). High-sensitivity m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ddc808927533cdefb8054c36222ab34
https://doi.org/10.1002/cyto.b.21853
https://doi.org/10.1002/cyto.b.21853
Publikováno v:
International Journal of Laboratory Hematology. 41:73-81
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare hematopoietic stem cell disorder resulting from the somatic mutation of the X-linked phosphatidyl-inositol glycan complementation Class A (PIG-A) gene. Depending on the severity of the mutation in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaf1631c031bf24d87ca83f884440a63
https://doi.org/10.1111/ijlh.13011
https://doi.org/10.1111/ijlh.13011
Autor:
Katherina Psarra, Ulrika Johansson, Kristy L. Wolniak, Sa A. Wang, Pedro Horna, Andrea Illingworth, Fiona E. Craig, Richard Torres, Julia Almeida
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
A peripheral blood flow cytometric assay for Sézary syndrome (SS) or circulating mycosis fungoides (MF) cells must be able to reliably identify, characterize, and enumerate T‐cells with an immunophenotype that differs from non‐neoplastic T‐cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6bbad4b63b5f9ea725baf7b9e1ecf97
https://pubmed.ncbi.nlm.nih.gov/32319723
https://pubmed.ncbi.nlm.nih.gov/32319723
Autor:
Iuri Marinov, Graeme Quest, D. Robert Sutherland, Fernando Ortiz, Miroslav Benko, Rakesh Nayyar, Andrea Illingworth
Publikováno v:
Cytometry Part B: Clinical Cytometry. 94:637-651
Background Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare acquired hematopoietic stem cell disorder characterized by an inability to make Glyco-Phosphatidyl-Inositol (GPI)-linked cell surface structures. Fluorescent proaerolysin (FLAER-Alexa488)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c80adf5b47217cc937354bf29f46ca33
https://doi.org/10.1002/cyto.b.21626
https://doi.org/10.1002/cyto.b.21626
Autor:
D. Robert Sutherland, Michael Keeney, Dan Payne, John Andreasen, Paul K. Wallace, Iuri Marinov, Andrea Illingworth, Fernando Ortiz
Publikováno v:
Cytometry Part B: Clinical Cytometry. 94:23-48
Since publication in 2010 of the International Clinical Cytometry Society (ICCS) Consensus Guidelines for detection of Paroxysmal nocturnal hemoglobinuria (PNH) by flow cytometery, a great deal of work has been performed to develop, optimize, and val
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc5d02aea9421d09f62c8085a45a537f
https://doi.org/10.1002/cyto.b.21610
https://doi.org/10.1002/cyto.b.21610
Autor:
D. Robert Sutherland, Orianne Wagner-Ballon, Iuri Marinov, Andrea Illingworth, Luigi DelVecchio
Publikováno v:
Cytometry Part B: Clinical Cytometry. 94:49-66
Over the past several years, a diverse group of physicians and other laboratory scientists have developed various recommendations and guidelines regarding best practices for PNH testing. This manuscript is based on these previous recommendations as w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66a635410d9a2ef78b0f7aa32c681181
https://doi.org/10.1002/cyto.b.21609
https://doi.org/10.1002/cyto.b.21609
Publikováno v:
Clinics in Laboratory Medicine. 37:855-867
Paroxysmal nocturnal hemoglobinuria (PNH) is an uncommon but frequently debilitating disease that, if untreated, may lead to death in up to 35% of patients within 5 years. Assessment of PNH clone size by flow cytometric analysis has increased in impo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd76b0f5731a361d9c4b45f2ea154cf9
https://doi.org/10.1016/j.cll.2017.07.007
https://doi.org/10.1016/j.cll.2017.07.007
Publikováno v:
European Journal of Haematology. 101:804-806
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::010f46781757e0342b2c304d84bdb348
https://doi.org/10.1111/ejh.13163
https://doi.org/10.1111/ejh.13163