Works matching IS 13899600 AND DT 2011 AND VI 10

Results: 94

Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 701, doi. 10.1007/s10689-011-9465-7

By:

Nielsen, Sarah;
Rubinstein, Wendy;
Thull, Darcy;
Armstrong, Michaele;
Feingold, Eleanor;
Yip, Linwah;
Tisherman, Samuel;
Carty, Sally

Publication type:

Article

Concerns about inherited risk of breast cancer prior to diagnosis in Japanese patients with breast complaints.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 681, doi. 10.1007/s10689-011-9464-8

By:

Ando, Noriko;
Iwamitsu, Yumi;
Kuranami, Masaru;
Okazaki, Shigemi;
Yamamoto, Kenji;
Watanabe, Masahiko;
Miyaoka, Hitoshi

Publication type:

Article

Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessment.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 649, doi. 10.1007/s10689-011-9462-x

By:

Ishii, Noriko;
Arai, Masami;
Koyama, Yurie;
Ueno, Masashi;
Yamaguchi, Toshiharu;
Kazuma, Keiko;
Muto, Tetsuichiro

Publication type:

Article

Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 633, doi. 10.1007/s10689-011-9459-5

By:

Petersen, Helle;
Esplen, Mary;
Ladelund, Steen;
Bernstein, Inge;
Sunde, Lone;
Carlsson, Christina;
Nilbert, Mef

Publication type:

Article

Abstracts.

Published in:: Familial Cancer, 2011, v. 10, n. 4, p. 713, doi. 10.1007/s10689-011-9492-4
Publication type:: Article

Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 273, doi. 10.1007/s10689-011-9431-4

By:

Hardt, Karin;
Heick, Sven;
Betz, Beate;
Goecke, Timm;
Yazdanparast, Haniyeh;
Küppers, Robin;
Servan, Kati;
Steinke, Verena;
Rahner, Nils;
Morak, Monika;
Holinski-Feder, Elke;
Engel, Christoph;
Möslein, Gabriela;
Schackert, Hans-Konrad;
Knebel Doeberitz, Magnus;
Pox, Christian;
Hegemann, Johannes;
Royer-Pokora, Brigitte

Publication type:

Article

Familial colorectal cancer type X syndrome: two distinct molecular entities?

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 623, doi. 10.1007/s10689-011-9473-7

By:

Francisco, Inês;
Albuquerque, Cristina;
Lage, Pedro;
Belo, Hélio;
Vitoriano, Inês;
Filipe, Bruno;
Claro, Isabel;
Ferreira, Sara;
Rodrigues, Paula;
Chaves, Paula;
Leitão, Carlos;
Pereira, António

Publication type:

Article

Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 691, doi. 10.1007/s10689-011-9472-8

By:

Villeneuve, Hugo;
Tremblay, Steve;
Galiatsatos, Polymnia;
Hamel, Nancy;
Guertin, Louis;
Morency, Renald;
Tischkowitz, Marc

Publication type:

Article

Microsatellite instability analysis in uterine cavity washings as a screening tool for endometrial cancer in Lynch syndrome.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 655, doi. 10.1007/s10689-011-9470-x

By:

Bouquier, Julie;
Blons, Hélène;
Narjoz, Céline;
Lécuru, Fabrice;
Laurent-Puig, Pierre;
Bats, Anne-Sophie

Publication type:

Article

A survey of APC mutations in Quebec.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 659, doi. 10.1007/s10689-011-9468-4

By:

Jarry, Jonathan;
Brunet, Jean-Sébastien;
Laframboise, Rachel;
Drouin, Régen;
Latreille, Jean;
Richard, Carole;
Gekas, Jean;
Maranda, Bruno;
Monczak, Yury;
Wong, Nora;
Pouchet, Carly;
Zaor, Sonya;
Kasprzak, Lidia;
Palma, Laura;
Wu, Mona;
Tischkowitz, Marc;
Foulkes, William;
Chong, George

Publication type:

Article

Identification of the deleterious 2080insA BRCA1 mutation in a male renal cell carcinoma patient from a family with multiple cancer diagnoses from Pakistan.

Published in:

2011

By:

Rashid, Muhammad;
Gull, Sidra;
Faisal, Saima;
Khaliq, Saba;
Asghar, Kashif;
Siddiqui, Neelam;
Amin, Asim;
Hamann, Ute

Publication type:

Letter

Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 695, doi. 10.1007/s10689-011-9466-6

By:

Siu, Wai;
Law, Chun;
Lam, Ching;
Mak, Chloe;
Wong, Gary;
Ho, Andrew;
Ho, Kwok;
Loo, Ka;
Chiu, Sin;
Chow, Louis;
Tong, Sui;
Chan, Albert

Publication type:

Article

Communication of BRCA1 and BRCA2 genetic test results to health care providers following genetic testing at a tertiary care center.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 673, doi. 10.1007/s10689-011-9460-z

By:

Ready, K.;
Arun, B.;
Schmeler, K.;
Uyei, A.;
Litton, J.;
Lu, K.;
Sun, C.;
Peterson, S.

Publication type:

Article

The identification and management of hereditary diffuse gastric cancer in a large Jordanian family.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 667, doi. 10.1007/s10689-011-9463-9

By:

Lynch, Henry;
Aldoss, Ibrahim;
Lynch, Jane

Publication type:

Article

Familial breast cancer: is it time to move from a reactive to a proactive role?

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 501, doi. 10.1007/s10689-011-9434-1

By:

Harris, H.;
Nippert, I.;
Julian-Reynier, C.;
Schmidtke, J.;
Asperen, C.;
Gadzicki, D.;
Tibben, A.;
Evans, D.

Publication type:

Article

Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 355, doi. 10.1007/s10689-010-9402-1

By:

Hensen, Erik;
Bayley, Jean-Pierre

Publication type:

Article

Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals.

Published in:

Familial Cancer, 2011, v. 10, n. 4, p. 641, doi. 10.1007/s10689-011-9461-y

By:

Valentin, Mev;
Silva, Felipe;
Santos, Erika;
Lisboa, Bianca;
Oliveira, Ligia;
Ferreira, Fabio;
Gomy, Israel;
Nakagawa, Wilson;
Aguiar Junior, Samuel;
Redal, Mariana;
Vaccaro, Carlos;
Valle, Adriana;
Sarroca, Carlos;
Carraro, Dirce;
Rossi, Benedito

Publication type:

Article

Progression of duodenal adenomatosis in familial adenomatous polyposis: due to ageing of subjects and advances in technology.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 491, doi. 10.1007/s10689-011-9433-2

By:

Mathus-Vliegen, Elisabeth;
Boparai, Karam;
Dekker, Evelien;
Geloven, Nan

Publication type:

Article

Case studies in the diagnosis and management of Peutz-Jeghers syndrome.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 463, doi. 10.1007/s10689-011-9438-x

By:

Riegert-Johnson, Douglas;
Roberts, Maegan;
Gleeson, Ferga;
Krishna, Murli;
Boardman, Lisa

Publication type:

Article

Serum levels of IGF-I and BRCA penetrance: a case control study in breast cancer families.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 521, doi. 10.1007/s10689-011-9437-y

By:

Pasanisi, Patrizia;
Bruno, Eleonora;
Venturelli, Elisabetta;
Manoukian, Siranoush;
Barile, Monica;
Peissel, Bernard;
Giacomi, Clelia;
Bonanni, Bernardo;
Berrino, Jacopo;
Berrino, Franco

Publication type:

Article

Gastrointestinal polyps and cancer in Peutz-Jeghers syndrome: clinical aspects.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 455, doi. 10.1007/s10689-011-9442-1

By:

Latchford, A.;
Phillips, R.

Publication type:

Article

Adequacy of risk-reducing gynaecologic surgery in BRCA1 or BRCA2 mutation carriers and other women at high risk of pelvic serous cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 505, doi. 10.1007/s10689-011-9435-0

By:

Kiely, B.;
Friedlander, M.;
Milne, R.;
Stanhope, L.;
Russell, P.;
Jenkins, M.;
Weideman, P.;
McLachlan, S.;
Grant, P.;
Hopper, J.;
Phillips, K.

Publication type:

Article

A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 515, doi. 10.1007/s10689-011-9436-z

By:

Kantelinen, Jukka;
Hansen, Thomas;
Kansikas, Minttu;
Krogh, Lotte;
Korhonen, Mari;
Ollila, Saara;
Nyström, Minna;
Gerdes, Anne-Marie;
Kariola, Reetta

Publication type:

Article

Dendritic cell and macrophage infiltration in microsatellite-unstable and microsatellite-stable colorectal cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 557, doi. 10.1007/s10689-011-9449-7

By:

Bauer, Kathrin;
Michel, Sara;
Reuschenbach, Miriam;
Nelius, Nina;
Knebel Doeberitz, Magnus;
Kloor, Matthias

Publication type:

Article

LKB1 as the ghostwriter of crypt history.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 437, doi. 10.1007/s10689-011-9469-3

By:

Jansen, Marnix;
Langeveld, Danielle;
Leng, Wendy;
Milne, Anya;
Giardiello, Francis;
Offerhaus, G.

Publication type:

Article

Management of renal tumors in Von Hippel-Lindau disease by percutaneous CT fluoroscopic guided radiofrequency ablation: preliminary results.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 529, doi. 10.1007/s10689-011-9440-3

By:

Iwamoto, Yoichi;
Kanda, Hideki;
Yamakado, Koichiro;
Soga, Norihito;
Arima, Kiminobu;
Takeda, Kan;
Sugimura, Yoshiki

Publication type:

Article

Cancer worry among Norwegian male BRCA1/2 mutation carriers.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 597, doi. 10.1007/s10689-011-9456-8

By:

Strømsvik, Nina;
Råheim, Målfrid;
Gjengedal, Eva

Publication type:

Article

The role of LKB1 in lung cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 447, doi. 10.1007/s10689-011-9443-0

By:

Sanchez-Cespedes, Montse

Publication type:

Article

LKB1 signaling in advancing cell differentiation.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 425, doi. 10.1007/s10689-011-9441-2

By:

Udd, Lina;
Mäkelä, Tomi

Publication type:

Article

Low penetrance hereditary retinoblastoma in a family: what should we consider in the genetic counselling process and follow up?

Published in:

2011

By:

Serrano, C.;
Alonso, J.;
Gómez-Mariano, G.;
Aguirre, E.;
Diez, O.;
Gadea, N.;
Bosch, N.;
Balmaña, J.;
Graña, B.

Publication type:

Letter

A cost-effectiveness analysis of prophylactic surgery versus gynecologic surveillance for women from hereditary non-polyposis colorectal cancer (HNPCC) Families.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 535, doi. 10.1007/s10689-011-9444-z

By:

Yang, Kathleen;
Caughey, Aaron;
Little, Sarah;
Cheung, Michael;
Chen, Lee-May

Publication type:

Article

The differential diagnosis of familial lentiginosis syndromes.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 481, doi. 10.1007/s10689-011-9446-x

By:

Lodish, Maya;
Stratakis, Constantine

Publication type:

Article

Attitudes toward childbearing and prenatal testing in individuals undergoing genetic testing for Lynch Syndrome.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 549, doi. 10.1007/s10689-011-9448-8

By:

Dewanwala, Akriti;
Chittenden, Anu;
Rosenblatt, Margery;
Mercado, Rowena;
Garber, Judy;
Syngal, Sapna;
Stoffel, Elena

Publication type:

Article

The sex ratio and age of onset features of gastric cancer patients in hereditary diffuse gastric cancer families.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 573, doi. 10.1007/s10689-011-9452-z

By:

Yu, Junxiu;
Li, Zhenfang

Publication type:

Article

A rationale for mTOR inhibitors as chemoprevention agents in Peutz-Jeghers syndrome.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 469, doi. 10.1007/s10689-011-9471-9

By:

Kuwada, Scott;
Burt, Randall

Publication type:

Article

Malignant fibrous histiocytoma is a rare Lynch syndrome-associated tumor in two German families.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 591, doi. 10.1007/s10689-011-9455-9

By:

Brieger, Angela;
Engels, Knut;
Schaefer, Dieter;
Plotz, Guido;
Zeuzem, Stefan;
Raedle, Jochen;
Trojan, Joerg

Publication type:

Article

A novel pathogenic germline mutation in the adenomatous polyposis coli gene in a Tunisian family with FAP.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 567, doi. 10.1007/s10689-011-9451-0

By:

Miladi-Abdennadher, Imen;
Amouri, Ali;
Ayadi, Lobna;
Khabir, Abdelmajid;
Ellouze, Sameh;
Tahri, Nabil;
Frikha, Mounir;
Sellami-Boudawara, Tahia;
Mokdad-Gargouri, Raja

Publication type:

Article

Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 545, doi. 10.1007/s10689-011-9447-9

By:

Yang, Xiaohong;
Jessop, Lea;
Myers, Timothy;
Amundadottir, Laufey;
Pfeiffer, Ruth;
Wheeler, William;
Pike, Kristen;
Yuenger, Jeff;
Burdett, Laurie;
Yeager, Meredith;
Chanock, Stephen;
Tucker, Margaret;
Goldstein, Alisa

Publication type:

Article

Factors associated with an individuals' decision to withdraw from genetic counseling for BRCA1 and BRCA2 genes mutations: are personality traits involved?

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 581, doi. 10.1007/s10689-011-9454-x

By:

Caruso, Anita;
Vigna, Cristina;
Bigazzi, Valentina;
Leone, Carlo;
Maggi, Gabriella;
Martayan, Aline;
Sega, Fabio;
Cognetti, Francesco;
Savarese, Antonella

Publication type:

Article

Peutz-Jeghers syndrome: a patient's view.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 473, doi. 10.1007/s10689-011-9453-y

By:

Sugars, Stephanie

Publication type:

Article

The LKB1 complex-AMPK pathway: the tree that hides the forest.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 415, doi. 10.1007/s10689-011-9457-7

By:

Sebbagh, Michaël;
Olschwang, Sylviane;
Santoni, Marie-Josée;
Borg, Jean-Paul

Publication type:

Article

Familial colorectal cancer: eleven years of data from a registry program in Switzerland.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 605, doi. 10.1007/s10689-011-9458-6

By:

Kovac, Michal;
Laczko, Endre;
Haider, Ritva;
Jiricny, Josef;
Mueller, Hansjakob;
Heinimann, Karl;
Marra, Giancarlo

Publication type:

Article

Lack of GNAQ germline mutations in uveal melanoma patients with high risk for hereditary cancer predisposition.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 319, doi. 10.1007/s10689-010-9401-2

By:

Abdel-Rahman, Mohamed;
Pilarski, Robert;
Massengill, James;
Christopher, Benjamin;
Davidorf, Frederick

Publication type:

Article

Introduction.

Published in:

Familial Cancer, 2011, v. 10, n. 3, p. 413, doi. 10.1007/s10689-011-9474-6

By:

Menko, Fred

Publication type:

Article

Mutation deep within an intron of MSH2 causes Lynch syndrome.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 297, doi. 10.1007/s10689-011-9427-0

By:

Clendenning, Mark;
Buchanan, Daniel;
Walsh, Michael;
Nagler, Belinda;
Rosty, Christophe;
Thompson, Bryony;
Spurdle, Amanda;
Hopper, John;
Jenkins, Mark;
Young, Joanne

Publication type:

Article

The impact of positive cancer family history on the clinical features and outcome of patients with non-small cell lung cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 331, doi. 10.1007/s10689-010-9403-0

By:

Li, Ning;
Shao, Kang;
Chen, Zhaoli;
Qiu, Bin;
Wang, Zhen;
Tan, Fengwei;
Wang, Jiwen;
Tan, Xiaogang;
Li, Baozhong;
Xiong, Meihua;
Zhou, Fang;
He, Jie

Publication type:

Article

Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 239, doi. 10.1007/s10689-010-9406-x

By:

Isinger-Ekstrand, Anna;
Therkildsen, Christina;
Bernstein, Inge;
Nilbert, Mef

Publication type:

Article

IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 173, doi. 10.1007/s10689-010-9404-z

By:

Henningson, Maria;
Hietala, Maria;
Törngren, Therese;
Olsson, Håkan;
Jernström, Helena

Publication type:

Article

Non-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis report.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 255, doi. 10.1007/s10689-010-9409-7

By:

Vogelsang, Matjaz;
Komel, Radovan

Publication type:

Article

PALB2 mutations in familial breast and pancreatic cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 225, doi. 10.1007/s10689-011-9426-1

By:

Hofstatter, Erin;
Domchek, Susan;
Miron, Alexander;
Garber, Judy;
Wang, Molin;
Componeschi, Kathryn;
Boghossian, Leigh;
Miron, Penelope;
Nathanson, Katherine;
Tung, Nadine

Publication type:

Article