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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004352naa a2200769 4500
001oai:lup.lub.lu.se:954f2854-6598-4f2d-94ad-7aef449a66b7
003SwePub
008160401s2009 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:118289370
024a https://lup.lub.lu.se/record/13748762 URI
024a https://doi.org/10.1038/leu.2008.3072 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1182893702 URI
040 a (SwePub)lud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a for2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Dispenzieri, A.4 aut
2451 0a International Myeloma Working Group guidelines for serum-free light chain analysis in multiple myeloma and related disorders
264 c 2008-11-20
264 1b Springer Science and Business Media LLC,c 2009
520 a The serum immunoglobulin-free light chain (FLC) assay measures levels of free kappa and lambda immunoglobulin light chains. There are three major indications for the FLC assay in the evaluation and management of multiple myeloma and related plasma cell disorders (PCD). In the context of screening, the serum FLC assay in combination with serum protein electrophoresis (PEL) and immunofixation yields high sensitivity, and negates the need for 24-h urine studies for diagnoses other than light chain amyloidosis (AL). Second, the baseline FLC measurement is of major prognostic value in virtually every PCD. Third, the FLC assay allows for quantitative monitoring of patients with oligosecretory PCD, including AL, oligosecretory myeloma and nearly two-thirds of patients who had previously been deemed to have non-secretory myeloma. In AL patients, serial FLC measurements outperform PEL and immunofixation. In oligosecretory myeloma patients, although not formally validated, serial FLC measurements reduce the need for frequent bone marrow biopsies. In contrast, there are no data to support using FLC assay in place of 24-h urine PEL for monitoring or for serial measurements in PCD with measurable disease by serum or urine PEL. This paper provides consensus guidelines for the use of this important assay, in the diagnosis and management of clonal PCD.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Cancer och onkologi0 (SwePub)302032 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cancer and Oncology0 (SwePub)302032 hsv//eng
653 a myeloma
653 a amyloid
653 a immunoglobulin-free light chain
653 a prognosis
700a Kyle, R.4 aut
700a Merlini, G.4 aut
700a Miguel, J. S.4 aut
700a Ludwig, H.4 aut
700a Hajek, R.4 aut
700a Palumbo, A.4 aut
700a Jagannath, S.4 aut
700a Blade, J.4 aut
700a Lonial, S.4 aut
700a Dimopoulos, M.4 aut
700a Comenzo, R.4 aut
700a Einsele, H.4 aut
700a Barlogie, B.4 aut
700a Anderson, K.4 aut
700a Gertz, M.4 aut
700a Harousseau, J. L.4 aut
700a Attal, M.4 aut
700a Tosi, P.4 aut
700a Sonneveld, P.4 aut
700a Boccadoro, M.4 aut
700a Morgan, G.4 aut
700a Richardson, P.4 aut
700a Sezer, O.4 aut
700a Mateos, M. V.4 aut
700a Cavo, M.4 aut
700a Joshua, D.4 aut
700a Turesson, Ingemaru Lund University,Lunds universitet,Institutionen för kliniska vetenskaper, Malmö,Medicinska fakulteten,Department of Clinical Sciences, Malmö,Faculty of Medicine4 aut0 (Swepub:lu)medf-itu
700a Chen, W.4 aut
700a Shimizu, K.4 aut
700a Powles, R.4 aut
700a Rajkumar, S. V.4 aut
700a Durie, B. G. M.4 aut
710a Institutionen för kliniska vetenskaper, Malmöb Medicinska fakulteten4 org
773t Leukemiad : Springer Science and Business Media LLCg 23:2, s. 215-224q 23:2<215-224x 1476-5551x 0887-6924
856u http://dx.doi.org/10.1038/leu.2008.307y FULLTEXT
856u https://www.nature.com/articles/leu2008307.pdf
8564 8u https://lup.lub.lu.se/record/1374876
8564 8u https://doi.org/10.1038/leu.2008.307
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:118289370

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