Zobrazeno 1 - 10
of 148
pro vyhledávání: '"paraproteinaemia"'
Publikováno v:
Thrombosis Journal, Vol 22, Iss 1, Pp 1-6 (2024)
Abstract Background Lupus anticoagulant (LA) is an in vitro phenomenon with prolongation of a phospholipid-dependent coagulation test which is not due to an inhibitor specific to a coagulation factor. Occasionally, addition of normal pooled plasma to
Externí odkaz:
https://doaj.org/article/de060efb93ee4f23bc560ee1c019f2be
Akademický článek
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Autor:
Alenka Matjašič, Karmen Wechtersbach, Rajko Kavalar, Matjaž Voršič, Jernej Mlakar, Janez Ravnik, Mara Popović
Publikováno v:
Folia Neuropathologica, Vol 59, Iss 2, Pp 205-211 (2021)
Light-chain deposition disease (LCDD), a rare type of monoclonal immunoglobulin deposition disease, can be presented as systemic or localized, very rarely affecting central nervous system (CNS). Only 10 cases of CNS-LCDD have been described so far. W
Externí odkaz:
https://doaj.org/article/d3f70ee8e9744a23a890d565ae506d8e
Publikováno v:
National Journal of Laboratory Medicine, Vol 10, Iss 4, Pp 01-03 (2021)
Amyloid Light chain (AL) amyloidosis is characterised by deposition of intact free light chains or their fragments in extracellular space. Here, authors describe the journey of a diagnostically challenging patient who presented with features of neph
Externí odkaz:
https://doaj.org/article/3fa28156b1c74cf1977c5018c1c4c3d1
Publikováno v:
Veterinární Medicína, Vol 61, Iss 9, Pp 475-496 (2016)
The evaluation of serum proteins and their electrophoretic pattern is a well-established laboratory method in the diagnosis of many diseases in humans, which has replaced the biochemical determination of the concentrations of albumin and the ratio of
Externí odkaz:
https://doaj.org/article/90af5c70ecf3474fae9ac58a2321b2b7
Autor:
Matthias Höpting, Ulrich Budde, Andreas Tiede, Matthias Grube, Joachim Hahn, Wolfgang Herr, Susanne Heimerl, Christina Hart
Publikováno v:
Acta Haematologica. 145:454-457
Acquired von Willebrand Syndrome (AVWS) is a rare coagulation disorder which can be associated with IgM paraproteinaemia. Recently, recombinant von Willebrand factor (rVWF) has become available for the treatment of bleedings in patients with inherite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38c4f1e91fad51620eaee0c6ed9602bb
https://doi.org/10.1159/000522236
https://doi.org/10.1159/000522236
Autor:
Mara Popović, Jernej Mlakar, Matjaž Voršič, Karmen Wechtersbach, Alenka Matjašič, Rajko Kavalar, Janez Ravnik
Publikováno v:
Folia Neuropathologica, Vol 59, Iss 2, Pp 205-211 (2021)
Light-chain deposition disease (LCDD), a rare type of monoclonal immunoglobulin deposition disease, can be presented as systemic or localized, very rarely affecting central nervous system (CNS). Only 10 cases of CNS-LCDD have been described so far. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::407a0b7ef6040e1222a63830a2e487e6
https://doi.org/10.5114/fn.2021.106405
https://doi.org/10.5114/fn.2021.106405
Akademický článek
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Autor:
Sanjay de Mel, Louis-Pierre Girard, Melissa Ooi, Li Mei Poon, Wee Joo Chng, Cinnie Yentia Soekojo
Publikováno v:
Cancers, Vol 12, Iss 1688, p 1688 (2020)
Cancers
Cancers
Monoclonal paraproteinaemia is an increasingly common reason for referral to haematology services. Paraproteinaemias may be associated with life-threatening haematologic malignancies but can also be an incidental finding requiring only observation. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::473b3203d1ae4119a65e3c3d22a33110
https://www.mdpi.com/2072-6694/12/6/1688
https://www.mdpi.com/2072-6694/12/6/1688
Autor:
Rachel Brown, Lionel Ginsberg
Publikováno v:
Journal of Neurology
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes) is a rare paraneoplastic syndrome, caused by a plasma cell proliferative disorder, which is most commonly lambda restricted. The neurological hallmark, which forms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddb750d1c6c3599f6395a3eada92e3cc
https://doi.org/10.1007/s00415-018-9110-6
https://doi.org/10.1007/s00415-018-9110-6