Works matching IS 13899600 AND DT 2013 AND VI 12

Results: 100

Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 675, doi. 10.1007/s10689-013-9644-9

By:

Sie, Aisha S.;
Prins, Judith B.;
Spruijt, Liesbeth;
Kets, C. Marleen;
Hoogerbrugge, Nicoline

Publication type:

Article

Case report: metachronous central nervous system desmoid tumours and thyroid carcinoma in a young familial adenomatous polyposis patient.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 647, doi. 10.1007/s10689-013-9640-0

By:

Butel-Simoes, G. I.;
Spigelman, A. D.

Publication type:

Article

The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer Sheraton Boston Hotel, Boston, Massachusetts, October 27–29, 2012.

Published in:: Familial Cancer, 2013, v. 12, n. 4, p. 779, doi. 10.1007/s10689-012-9592-9
Publication type:: Article

Chemoprevention in Lynch syndrome.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 707, doi. 10.1007/s10689-013-9650-y

By:

Burn, John;
Mathers, John C.;
Bishop, D. Tim

Publication type:

Article

Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 657, doi. 10.1007/s10689-013-9642-y

By:

Zhu, Jie;
Cui, Liang;
Wang, Wei;
Hang, Xing-Yi;
Xu, A-Xiang;
Yang, Su-Xia;
Dou, Jing-Tao;
Mu, Yi-Ming;
Zhang, Xu;
Gao, Jiang-Ping

Publication type:

Article

Rectal cancers in patients with familial adenomatous polyposis.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 749, doi. 10.1007/s10689-013-9656-5

By:

Liang, Jennifer;
Church, James M.

Publication type:

Article

Polymorphisms in arachidonic acid metabolism-related genes and the risk and prognosis of colorectal cancer.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 755, doi. 10.1007/s10689-013-9659-2

By:

Li, Shuying;
Zhao, Xiaojuan;
Wu, Zhiwei;
Li, Ye;
Zhu, Lin;
Cui, Binbin;
Dong, Xinshu;
Tian, Suli;
Hu, Fulan;
Zhao, Yashuang

Publication type:

Article

Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 639, doi. 10.1007/s10689-013-9628-9

By:

Aktan-Collan, Katja;
Kääriäinen, Helena;
Järvinen, Heikki;
Peltomäki, Päivi;
Pylvänäinen, Kirsi;
Mecklin, Jukka-Pekka;
Haukkala, Ari

Publication type:

Article

The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia.

Published in:

2013

By:

Teo, Zhi L.;
Sawyer, Sarah D.;
James, Paul A.;
Mitchell, Gillian;
Trainer, Alison H.;
Lindeman, Geoffrey J.;
Shackleton, Kylie;
Cicciarelli, Linda;
Southey, Melissa C.

Publication type:

Letter

Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 767, doi. 10.1007/s10689-013-9622-2

By:

de Juan Jiménez, Inmaculada;
García Casado, Zaida;
Palanca Suela, Sarai;
Esteban Cardeñosa, Eva;
López Guerrero, José Antonio;
Segura Huerta, Ángel;
Chirivella González, Isabel;
Sánchez Heras, Ana Beatriz;
Juan Fita, Mª José;
Tena García, Isabel;
Guillen Ponce, Carmen;
Martínez de Dueñas, Eduardo;
Romero Noguera, Ignacio;
Salas Trejo, Dolores;
Goicoechea Sáez, Mercedes;
Bolufer Gilabert, Pascual

Publication type:

Article

Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 741, doi. 10.1007/s10689-013-9652-9

By:

Farrell, M. P.;
Hughes, D. J.;
Drost, M.;
Wallace, A. J.;
Cummins, R. J.;
Fletcher, T. A.;
Meany, M. A.;
Kay, E. W.;
de Wind, N.;
Power, D. G.;
Andrews, E. J.;
Green, A. J.;
Gallagher, D. J.

Publication type:

Article

Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 601, doi. 10.1007/s10689-013-9621-3

By:

Lapointe, Julie;
Dorval, Michel;
Noguès, Catherine;
Fabre, Roxane;
Julian-Reynier, Claire

Publication type:

Article

Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 597, doi. 10.1007/s10689-013-9618-y

By:

Alanee, Shaheen;
Shah, Sohela;
Vijai, Joseph;
Schrader, Kasmintan;
Hamilton, Robert;
Rau-Murthy, Rohini;
Sarrel, Kara;
Manschreck, Christopher;
Eastham, James;
Offit, Kenneth

Publication type:

Article

Self administered screening for hereditary cancers in conjunction with mammography and ultrasound.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 651, doi. 10.1007/s10689-013-9641-z

By:

McDonnell, Charles H.;
Seidenwurm, David J.;
McDonnell, Diana E.;
Bobolis, Kristie A.

Publication type:

Article

Interest of individuals from BRCA families to participate in research studies focused on male BRCA carriers.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 615, doi. 10.1007/s10689-013-9624-0

By:

Pal, Tuya;
Vadaparampil, Susan;
Kim, Jongphil;
Xu, Yan;
Friedman, Sue;
Narod, Steven A.;
Metcalfe, Kelly

Publication type:

Article

Do individuals with a family history of colorectal cancer adhere to medical recommendations for the prevention of colorectal cancer?

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 629, doi. 10.1007/s10689-013-9627-x

By:

Bronner, Karen;
Mesters, Ilse;
Weiss-Meilnik, Ahuva;
Geva, Ravit;
Rozner, Guy;
Strul, Hana;
Inbar, Moshe;
Halpern, Zamir;
Kariv, Revital

Publication type:

Article

A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 573, doi. 10.1007/s10689-012-9587-6

By:

Ponz de Leon, Maurizio;
Bertarelli, Claudia;
Casadei, Gian;
Grilli, Andrea;
Bacchini, Patrizia;
Pedroni, Monica;
Jovine, Elio

Publication type:

Article

Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with BRCA gene mutation.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 621, doi. 10.1007/s10689-013-9625-z

By:

Kim, Dongwon;
Kang, Eunyoung;
Hwang, Euijun;
Sun, Young;
Hwang, Yoonsun;
Yom, Cha Kyong;
Kim, Kidong;
No, Jae Hong;
Kim, Yong-Beom;
Kim, Sung-Won

Publication type:

Article

Extracolonic cancer risk in patients with serrated polyposis syndrome and their first-degree relatives.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 669, doi. 10.1007/s10689-013-9643-x

By:

Hazewinkel, Yark;
Reitsma, Johannes B.;
Nagengast, Fokko M.;
Vasen, Hans F.;
van Os, Theo A. M.;
van Leerdam, Monique E.;
Koornstra, Jan-Jacob;
Dekker, Evelien

Publication type:

Article

Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 611, doi. 10.1007/s10689-013-9623-1

By:

Fujii, Katsunori;
Ohashi, Hirofumi;
Suzuki, Maiko;
Hatsuse, Hiromi;
Shiohama, Tadashi;
Uchikawa, Hideki;
Miyashita, Toshiyuki

Publication type:

Article

Underestimated survival predictions of the prognostic tools Adjuvant! Online and PREDICT in BRCA1-associated breast cancer patients.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 683, doi. 10.1007/s10689-013-9646-7

By:

Plakhins, Grigorijs;
Irmejs, Arvids;
Gardovskis, Andris;
Subatniece, Signe;
Liepniece-Karele, Inta;
Purkalne, Gunta;
Teibe, Uldis;
Trofimovics, Genadijs;
Miklasevics, Edvins;
Gardovskis, Janis

Publication type:

Article

Searching for E-cadherin gene mutations in early onset diffuse gastric cancer and hereditary diffuse gastric cancer in Korean patients.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 503, doi. 10.1007/s10689-012-9595-6

By:

Kim, Sollip;
Chung, Jun-Won;
Jeong, Tae-Dong;
Park, Young-Soo;
Lee, Jeong;
Ahn, Ji;
Kim, Do;
Choi, Kee;
Lee, Woochang;
Song, Ho;
Lee, Gin;
Chun, Sail;
Jung, Hwoon-Yong;
Min, Won-Ki;
Kim, Jin-Ho

Publication type:

Article

Familial adenomatous polyposis: not all masses are desmoids.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 525, doi. 10.1007/s10689-012-9580-0

By:

Sloane, J.;
Ranchod, P.;
Williams, G.;
Clark, S.

Publication type:

Article

Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 563, doi. 10.1007/s10689-012-9597-4

By:

Clendenning, Mark;
Walsh, Michael;
Gelpi, Judith;
Thibodeau, Stephen;
Lindor, Noralane;
Potter, John;
Newcomb, Polly;
LeMarchand, Loic;
Haile, Robert;
Gallinger, Steve;
Hopper, John;
Jenkins, Mark;
Rosty, Christophe;
Young, Joanne;
Buchanan, Daniel

Publication type:

Article

Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 691, doi. 10.1007/s10689-013-9647-6

By:

Bielinska, Beata;
Gaj, Pawel;
Kluska, Anna;
Nowakowska, Dorota;
Balabas, Aneta;
Dabrowska, Michalina;
Niwinska, Anna;
Gruchota, Jakub;
Zub, Renata;
Skasko, Elzbieta;
Steffen, Jan;
Ostrowski, Jerzy;
Siedlecki, Janusz A.

Publication type:

Article

“High rate of recurrent adenomatosis during endoscopic surveillance after duodenectomy in patients with familial adenomatous polyposis”.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 699, doi. 10.1007/s10689-013-9648-5

By:

Alderlieste, Yasser A.;
Bastiaansen, Barbara A.;
Mathus-Vliegen, Elisabeth M. H.;
Gouma, Dirk J.;
Dekker, Evelien

Publication type:

Article

Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry.

Published in:

Familial Cancer, 2013, v. 12, n. 4, p. 719, doi. 10.1007/s10689-013-9651-x

By:

Casey, Murray Joseph;
Bewtra, Chhanda;
Lynch, Henry T.;
Snyder, Carrie;
Stacy, Mark;
Watson, Patrice

Publication type:

Article

Erratum to: Birt-Hogg-Dubé syndrome: from gene discovery to molecularly targeted therapies.

Published in:

2013

By:

Schmidt, Laura

Publication type:

Correction Notice

Mutation screening in a Norwegian cohort with pheochromocytoma.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 529, doi. 10.1007/s10689-013-9608-0

By:

Sjursen, Wenche;
Halvorsen, Henrik;
Hofsli, Eva;
Bachke, Siri;
Berge, Åsa;
Engebretsen, Lars;
Falkmer, Sture;
Falkmer, Ursula;
Varhaug, Jan

Publication type:

Article

Birt-Hogg-Dubé: tumour suppressor function and signalling dynamics central to folliculin.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 367, doi. 10.1007/s10689-012-9576-9

By:

Tee, Andrew;
Pause, Arnim

Publication type:

Article

The prognostic value of MGMT promoter methylation in Glioblastoma multiforme: a meta-analysis.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 449, doi. 10.1007/s10689-013-9607-1

By:

Zhang, Kui;
Wang, Xiao-qin;
Zhou, Bin;
Zhang, Lin

Publication type:

Article

Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern India.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 489, doi. 10.1007/s10689-012-9590-y

By:

Chakraborty, Abhijit;
Mukhopadhyay, Ashis;
Bhattacharyya, Deboshree;
Bose, Chinmoy;
Choudhuri, Keya;
Mukhopadhyay, Soma;
Basak, Jayasri

Publication type:

Article

Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 537, doi. 10.1007/s10689-013-9609-z

By:

Montgomery, Susan;
Barsevick, Andrea;
Egleston, Brian;
Bingler, Ruth;
Ruth, Karen;
Miller, Suzanne;
Malick, John;
Cescon, Terrence;
Daly, Mary

Publication type:

Article

Birt-Hogg-Dubé syndrome and the skin.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 381, doi. 10.1007/s10689-013-9600-8

By:

Vernooij, Marigje;
Claessens, Tijs;
Luijten, Monique;
Steensel, Maurice;
Coull, Barry

Publication type:

Article

A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 373, doi. 10.1007/s10689-012-9593-8

By:

Menko, Fred;
Johannesma, Paul;
Moorselaar, R.;
Reinhard, Rinze;
Waesberghe, Jan;
Thunnissen, Erik;
Houweling, Arjan;
Leter, Edward;
Waisfisz, Quinten;
Doorn, Martijn;
Starink, Theo;
Postmus, Pieter;
Coull, Barry;
Steensel, Maurice;
Gille, Johan

Publication type:

Article

Abstracts.

Published in:: Familial Cancer, 2013, v. 12, n. 3, p. 405, doi. 10.1007/s10689-013-9678-z
Publication type:: Article

Unmet support needs and distress among women with a BRCA1/ 2 mutation.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 509, doi. 10.1007/s10689-012-9596-5

By:

Farrelly, Ashley;
White, Victoria;
Meiser, Bettina;
Jefford, Michael;
Young, Mary-Anne;
Ieropoli, Sandra;
Winship, Ingrid;
Duffy, Jessica

Publication type:

Article

A complex endocrine conundrum.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 577, doi. 10.1007/s10689-012-9594-7

By:

Bano, G.;
Siedel, V.;
Beharry, N.;
Wilson, P.;
Cranston, T.;
Hodgson, S.

Publication type:

Article

Erratum to: Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis.

Published in:

2013

By:

Jasperson, Kory;
Vu, Thuy;
Schwab, Angela;
Neklason, Deborah;
Rodriguez-Bigas, Miguel;
Burt, Randall;
Weitzel, Jeffrey

Publication type:

Correction Notice

Birt-Hogg-Dubé syndrome.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 355, doi. 10.1007/s10689-013-9679-y

By:

Czyzyk-Krzeska, Maria;
McCormack, Francis

Publication type:

Article

Detection of large deletions in the VHL gene using a Real-Time PCR with SYBR Green.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 519, doi. 10.1007/s10689-013-9606-2

By:

Ebenazer, Andrew;
Rajaratnam, Simon;
Pai, Rekha

Publication type:

Article

Splice site mutations in mismatch repair genes and risk of cancer in the general population.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 567, doi. 10.1007/s10689-013-9601-7

By:

Thomsen, Mette;
Nordestgaard, Børge;
Tybjærg-Hansen, Anne;
Bojesen, Stig

Publication type:

Article

Erratum to: Closing the loop: an interactive action research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial needs post-genetic cancer risk assessment.

Published in:

2013

By:

MacDonald, Deborah;
Deri, Julia;
Ricker, Charité;
Perez, Martin;
Ogaz, Raquel;
Feldman, Nancy;
Viveros, Lori;
Paz, Benjamin;
Weitzel, Jeffrey;
Blazer, Kathleen

Publication type:

Correction Notice

Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 555, doi. 10.1007/s10689-013-9617-z

By:

Cruz-Correa, Marcia;
Diaz-Algorri, Yaritza;
Mendez, Vanessa;
Vazquez, Pedro;
Lozada, Maria;
Freyre, Katerina;
Lathroum, Liselle;
Gonzalez-Pons, Maria;
Hernandez-Marrero, Jessica;
Giardiello, Francis;
Rodriguez-Quilichini, Segundo

Publication type:

Article

Erratum to: Birt-Hogg-Dubé: beyond the clinical manifestations.

Published in:

2013

By:

Middelton, Lindsay

Publication type:

Correction Notice

Body image issues after bilateral prophylactic mastectomy with breast reconstruction in healthy women at risk for hereditary breast cancer.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 479, doi. 10.1007/s10689-012-9588-5

By:

Gopie, Jessica;
Mureau, Marc;
Seynaeve, Caroline;
ter Kuile, Moniek;
Menke-Pluymers, Marian;
Timman, Reinier;
Tibben, Aad

Publication type:

Article

Mutation screen and RNA analysis disclose the changed splicing of the E-cadherin transcription in gastric cancer.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 547, doi. 10.1007/s10689-013-9619-x

By:

Li, Xiaowei;
Gao, Yafan;
Pan, Yiyuan;
Pan, Yan;
Wang, Lifeng;
Xiao, Nong;
He, Qiong;
Fan, Yimei;
Wang, Yaping

Publication type:

Article

Birt-Hogg-Dubé syndrome: from gene discovery to molecularly targeted therapies.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 357, doi. 10.1007/s10689-012-9574-y

By:

Schmidt, Laura

Publication type:

Article

The risk of gastric cancer in carriers of CHEK2 mutations.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 473, doi. 10.1007/s10689-012-9599-2

By:

Teodorczyk, Urszula;
Cybulski, Cezary;
Wokołorczyk, Dominika;
Jakubowska, Anna;
Starzyńska, Teresa;
Ławniczak, Małgorzata;
Domagała, Paweł;
Ferenc, Katarzyna;
Marlicz, Krzysztof;
Banaszkiewicz, Zbigniew;
Wiśniowski, Rafał;
Narod, Steven;
Lubiński, Jan

Publication type:

Article

Cancer family history triage: a key step in the decision to offer screening and genetic testing.

Published in:

Familial Cancer, 2013, v. 12, n. 3, p. 497, doi. 10.1007/s10689-012-9589-4

By:

Brennan, Paul;
Claber, Oonagh;
Brennan, Tracey

Publication type:

Article