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Sökning: WFRF:(Bishop C) > (2005-2009) > Selection criteria ...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004409naa a2200769 4500
001oai:lup.lub.lu.se:06524336-ca99-43e6-b26f-e3628726362a
003SwePub
008160401s2009 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/14895452 URI
024a https://doi.org/10.1016/j.jaad.2009.03.0162 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a for2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Leachman, Sancy A.4 aut
2451 0a Selection criteria for genetic assessment of patients with familial melanoma
264 1b Elsevier BV,c 2009
520 a Approximately 5% to 10% of melanoma may be hereditary in nature, and about 2% of melanoma can be specifically attributed to pathogenic germline mutations in cyclin-dependent kinase inhibitor 2A (CDKN2A). To appropriately identify the small proportion of patients Who benefit most from referral to a genetics specialist for consideration of genetic testing for CDKN2A, We have reviewed available published studies of CDKN2A mutation analysis in cohorts with invasive, cutaneous melanoma and found variability in the rate of CDKN2A mutations based on geography, ethnicity, and the type of study and eligibility criteria used. Except in regions of high melanoma incidence, such as Australia, we found higher rates of CDKN2A positivity in individuals with 3 or more primary invasive melanomas and/or families with at least one invasive melanoma and two or more other diagnoses of invasive melanoma and/or pancreatic cancer among first- or second-degree relatives on the same side of the family. The Work summarized in this review should help identify individuals who are appropriate candidates for referral for genetic consultation and possible testing. (J Am Acad Dermatol 2009;61:677-84.)
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Dermatologi och venereologi0 (SwePub)302042 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Dermatology and Venereal Diseases0 (SwePub)302042 hsv//eng
653 a genetic testing
653 a genetic counseling
653 a CDKN2A
653 a familial
653 a hereditary
653 a melanoma
653 a p16
700a Carucci, John4 aut
700a Kohlmann, Wendy4 aut
700a Banks, Kimberly C.4 aut
700a Asgari, Maryam M.4 aut
700a Bergman, Wilma4 aut
700a Bianchi-Scarra, Giovanna4 aut
700a Brentnall, Teresa4 aut
700a Bressac-de Paillerets, Brigitte4 aut
700a Bruno, William4 aut
700a Curiel-Lewandrowski, Clara4 aut
700a de Snoo, Femke A.4 aut
700a Debniak, Tadeusz4 aut
700a Demierre, Marie-France4 aut
700a Elder, David4 aut
700a Goldstein, Alisa M.4 aut
700a Grant-Kels, Jane4 aut
700a Halpern, Allan C.4 aut
700a Ingvar, Christianu Lund University,Lunds universitet,Kirurgi, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Surgery (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine4 aut0 (Swepub:lu)kir-cin
700a Kefford, Richard F.4 aut
700a Lang, Julie4 aut
700a MacKie, Rona M.4 aut
700a Mann, Graham J.4 aut
700a Mueller, Kurt4 aut
700a Newton-Bishop, Julia4 aut
700a Olsson, Håkanu Lund University,Lunds universitet,Medicinsk onkologi,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Medical oncology,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine4 aut0 (Swepub:lu)onk-hol
700a Peterson, Gloria M.4 aut
700a Puig, Susana4 aut
700a Rigel, Darrell4 aut
700a Swetter, Susan M.4 aut
700a Tucker, Margaret A.4 aut
700a Yakobson, Emanuel4 aut
700a Zitelli, John A.4 aut
700a Tsao, Hensin4 aut
710a Kirurgi, Lundb Sektion V4 org
773t Journal of American Academy of Dermatologyd : Elsevier BVg 61:4, s. 677-684q 61:4<677-684x 0190-9622
856u http://dx.doi.org/10.1016/j.jaad.2009.03.016y FULLTEXT
856u https://europepmc.org/articles/pmc3307795?pdf=render
8564 8u https://lup.lub.lu.se/record/1489545
8564 8u https://doi.org/10.1016/j.jaad.2009.03.016

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