Sökning: WFRF:(Bishop C) > (2005-2009) > Selection criteria ...
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000 | 04409naa a2200769 4500 | |
001 | oai:lup.lub.lu.se:06524336-ca99-43e6-b26f-e3628726362a | |
003 | SwePub | |
008 | 160401s2009 | |||||||||||000 ||eng| | |
024 | 7 | a https://lup.lub.lu.se/record/14895452 URI |
024 | 7 | a https://doi.org/10.1016/j.jaad.2009.03.0162 DOI |
040 | a (SwePub)lu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a for2 swepub-publicationtype |
072 | 7 | a ref2 swepub-contenttype |
100 | 1 | a Leachman, Sancy A.4 aut |
245 | 1 0 | a Selection criteria for genetic assessment of patients with familial melanoma |
264 | 1 | b 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 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Dermatologi och venereologi0 (SwePub)302042 hsv//swe |
650 | 7 | a 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 | |
700 | 1 | a Carucci, John4 aut |
700 | 1 | a Kohlmann, Wendy4 aut |
700 | 1 | a Banks, Kimberly C.4 aut |
700 | 1 | a Asgari, Maryam M.4 aut |
700 | 1 | a Bergman, Wilma4 aut |
700 | 1 | a Bianchi-Scarra, Giovanna4 aut |
700 | 1 | a Brentnall, Teresa4 aut |
700 | 1 | a Bressac-de Paillerets, Brigitte4 aut |
700 | 1 | a Bruno, William4 aut |
700 | 1 | a Curiel-Lewandrowski, Clara4 aut |
700 | 1 | a de Snoo, Femke A.4 aut |
700 | 1 | a Debniak, Tadeusz4 aut |
700 | 1 | a Demierre, Marie-France4 aut |
700 | 1 | a Elder, David4 aut |
700 | 1 | a Goldstein, Alisa M.4 aut |
700 | 1 | a Grant-Kels, Jane4 aut |
700 | 1 | a Halpern, Allan C.4 aut |
700 | 1 | a 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 |
700 | 1 | a Kefford, Richard F.4 aut |
700 | 1 | a Lang, Julie4 aut |
700 | 1 | a MacKie, Rona M.4 aut |
700 | 1 | a Mann, Graham J.4 aut |
700 | 1 | a Mueller, Kurt4 aut |
700 | 1 | a Newton-Bishop, Julia4 aut |
700 | 1 | a 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 |
700 | 1 | a Peterson, Gloria M.4 aut |
700 | 1 | a Puig, Susana4 aut |
700 | 1 | a Rigel, Darrell4 aut |
700 | 1 | a Swetter, Susan M.4 aut |
700 | 1 | a Tucker, Margaret A.4 aut |
700 | 1 | a Yakobson, Emanuel4 aut |
700 | 1 | a Zitelli, John A.4 aut |
700 | 1 | a Tsao, Hensin4 aut |
710 | 2 | a Kirurgi, Lundb Sektion V4 org |
773 | 0 | t Journal of American Academy of Dermatologyd : Elsevier BVg 61:4, s. 677-684q 61:4<677-684x 0190-9622 |
856 | 4 | u http://dx.doi.org/10.1016/j.jaad.2009.03.016y FULLTEXT |
856 | 4 | u https://europepmc.org/articles/pmc3307795?pdf=render |
856 | 4 8 | u https://lup.lub.lu.se/record/1489545 |
856 | 4 8 | u https://doi.org/10.1016/j.jaad.2009.03.016 |
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