Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sajjan Mittal"'
Autor:
Daniele Avenoso, Judith C.W. Marsh, Victoria Potter, Antonio Pagliuca, Simon Slade, Fiona Dignan, Eleni Tholouli, Sajjan Mittal, Bernard Davis, Sudhir Tauro, Rachel Kesse-Adu, Morag Griffin, Elspeth Payne, Shreyans Gandhi, Austin G. Kulasekararaj
Publikováno v:
Haematologica, Vol 107, Iss 2 (2021)
Externí odkaz:
https://doaj.org/article/893a5480d9734c388f5b35372654d6b9
Publikováno v:
Haematologica, Vol 93, Iss 1 (2008)
Minor CLL-like clones are found in ~3% of healthy individuals. AIHA and ITP are common in CLL and may be causally linked. We investigated the presence of CLL phenotype lymphocytes in 11 cases of primary AIHA, 18 of ITP and 2 of Evans’ Syndrome, com
Externí odkaz:
https://doaj.org/article/f14c6852c30640e1892a50fa99d057d2
Autor:
Austin G. Kulasekararaj, Antonio Pagliuca, Bernard A. Davis, Judith C. W. Marsh, Victoria Potter, Sudhir Tauro, Eleni Tholouli, Morag Griffin, Fiona L Dignan, Rachel Kesse-Adu, Simon Slade, Daniele Avenoso, Sajjan Mittal, Elspeth Payne, Shreyans Gandhi
Publikováno v:
Haematologica. 107:541-543
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cf36cb85e9a3b4650e35dd3ee0f6f6a
https://doi.org/10.3324/haematol.2021.279928
https://doi.org/10.3324/haematol.2021.279928
Autor:
David Wrench, Gary Middleton, Gordon Cook, Abigail Gault, Jonathan Carmichael, John Ashcroft, Rachel Kerr, Helen Curley, Austin G. Kulasekararaj, Neil Rabin, Helen S. Oram, Jack Illingworth, Roland Arnold, Ruth Pettengell, Tom Newsom-Davies, Jane Apperly, Michael Tilby, Graham P. Collins, Oliver Tomkins, Karin Purshouse, Stephen Booth, Mohammed Altohami, Jean-Baptiste Cazier, Lucy Cook, Andrew J. Innes, Naomi A. Campton, James Aries, Sam Moody, Tania Tillet, Lennard Y. W. Lee, Sajjan Mittal, Claire Palles, Saoirse Dolly, Leena Mukherjee, Csilla Várnai
Publikováno v:
British Journal of Haematology
Summary Patients with haematological malignancies have a high risk of severe infection and death from SARS‐CoV‐2. In this prospective observational study, we investigated the impact of cancer type, disease activity, and treatment in 877 unvaccina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::909d7699aec0e45797454875fdbabc5e
http://hdl.handle.net/10044/1/98130
http://hdl.handle.net/10044/1/98130
Autor:
Sajjan Mittal
Amyloidosis is a multisystem disease caused by the extracellular deposition of insoluble abnormal fibrils that injure tissues and organs. The fibrils are formed by the aggregation of misfolded, normally soluble proteins. Systemic amyloid light-chain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51b6bf6f2e1b8658473fe4134bbe0ecb
https://doi.org/10.1093/med/9780199568741.003.0181
https://doi.org/10.1093/med/9780199568741.003.0181
Publikováno v:
Critical Reviews in Oncology/Hematology. 65:101-108
Immunotherapy offers the potential for cure of malignancy without the side effects too commonly seen with conventional chemotherapy. The efficacy of allogenic transplantation and monoclonal antibodies in hematological malignancies illustrate this pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5c2c596c859e3d8407f4a778cd4fa6d
https://doi.org/10.1016/j.critrevonc.2007.05.004
https://doi.org/10.1016/j.critrevonc.2007.05.004
Publikováno v:
European Journal of Haematology. 76:531-534
Hepatosplenic gamma-delta T-cell lymphoma is a rare, usually fatal lymphoma and available literature on management is sparse. Allografting is probably the only curative option. We describe a further case with a dramatic, though transient response to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9832a54ae76b39271070023cd1a9a30
https://doi.org/10.1111/j.1600-0609.2006.00646.x
https://doi.org/10.1111/j.1600-0609.2006.00646.x
Autor:
Sajjan Mittal, Henry G. Watson
Publikováno v:
British Journal of Haematology. 133:355-363
Recombinant activated factor VII (rVIIa) was initially used for the treatment of inhibitors in patients with haemophilia. However, its localised mode of action at sites of damage to the vessel combined with dramatic clinical observations in exsanguin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4e3cdefb66c26f3cdc10b175f8a4638
https://doi.org/10.1111/j.1365-2141.2006.06023.x
https://doi.org/10.1111/j.1365-2141.2006.06023.x
Publikováno v:
Clinical and Laboratory Haematology. 27:402-404
The spectrum of clinical presentation of haematological disease is wide. We highlight two features of this principle: a rare cause of a 'haematological' presentation and a possible haematological cause of a disease not normally considered as such. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55c1db751b1996393c68f0fd9b74338b
https://doi.org/10.1111/j.1365-2257.2005.00730.x
https://doi.org/10.1111/j.1365-2257.2005.00730.x
Publikováno v:
British journal of haematology. 156(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0fc98407faa30953d648e6d3c8781204
https://pubmed.ncbi.nlm.nih.gov/22224922
https://pubmed.ncbi.nlm.nih.gov/22224922