Works matching IS 13899600 AND DT 2011 AND VI 10 AND IP 2

Results: 30

Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 315, doi. 10.1007/s10689-010-9405-y

By:

Sabbaghian, N.;
Kyle, R.;
Hao, A.;
Hogg, D.;
Tischkowitz, M.

Publication type:

Article

German national case collection for familial pancreatic cancer (FaPaCa): ten years experience.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 323, doi. 10.1007/s10689-010-9414-x

By:

Schneider, Ralph;
Slater, Emily;
Sina, Mercede;
Habbe, Nils;
Fendrich, Volker;
Matthäi, Elvira;
Langer, Peter;
Bartsch, Detlef

Publication type:

Article

The impact of cancer pathology confirmation on clinical management of a family history of cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 373, doi. 10.1007/s10689-010-9407-9

By:

Edwards, E.;
Lucassen, A.

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

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

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

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

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

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

Familial gastric cancer: update for practice management.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 391, doi. 10.1007/s10689-010-9410-1

By:

Corso, Giovanni;
Marrelli, Daniele;
Roviello, Franco

Publication type:

Article

A new frameshift MEN1 gene mutation associated with familial malignant insulinomas.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 343, doi. 10.1007/s10689-010-9412-z

By:

Hasani-Ranjbar, Shirin;
Amoli, Mahsa;
Ebrahim-Habibi, Azadeh;
Gozashti, Mohammad;
Khalili, Nahid;
Sayyahpour, Forugh;
Hafeziyeh, Jila;
Soltani, Akbar;
Larijani, Bagher

Publication type:

Article

Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 337, doi. 10.1007/s10689-010-9411-0

By:

Slade, Ingrid;
Murray, Anne;
Hanks, Sandra;
Kumar, Ajith;
Walker, Lisa;
Hargrave, Darren;
Douglas, Jenny;
Stiller, Charles;
Izatt, Louise;
Rahman, Nazneen

Publication type:

Article

Case report: renal cell carcinoma segregating with a t(2;3)(q37.3;q13.2) chromosomal translocation in an Ashkenazi Jewish family.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 349, doi. 10.1007/s10689-010-9413-y

By:

McKay, L.;
Frydenberg, M.;
Lipton, L.;
Norris, F.;
Winship, I.

Publication type:

Article

Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome).

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 245, doi. 10.1007/s10689-010-9408-8

By:

Roberts, Aedan;
Nancarrow, Derek;
Clendenning, Mark;
Buchanan, Daniel;
Jenkins, Mark;
Duggan, David;
Taverna, Darin;
McKeone, Diane;
Walters, Rhiannon;
Walsh, Michael;
Young, Bruce;
Jass, Jeremy;
Rosty, Christophe;
Gattas, Michael;
Pelzer, Elise;
Hopper, John;
Goldblatt, Jack;
George, Jill;
Suthers, Graeme;
Phillips, Kerry

Publication type:

Article

Adrenocortical carcinoma, an unusual extracolonic tumor associated with Lynch II syndrome.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 265, doi. 10.1007/s10689-010-9416-8

By:

Medina-Arana, V.;
Delgado, L.;
González, L.;
Bravo, A.;
Díaz, H.;
Salido, E.;
Riverol, D.;
González-Aguilera, J.;
Fernández-Peralta, A.

Publication type:

Article

Early occurrence of lung adenocarcinoma and breast cancer after radiotherapy of a chest wall sarcoma in a patient with a de novo germline mutation in TP53.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 187, doi. 10.1007/s10689-010-9415-9

By:

Ferrarini, Alessandra;
Auteri-Kaczmarek, Agnes;
Pica, Alessia;
Boesch, Nemya;
Heinimann, Karl;
Schäfer, Stephan;
Vesnaver-Megalo, Sara;
Cina, Viviane;
Beckmann, Jacques;
Monnerat, Christian

Publication type:

Article

Impact of computer-assisted data collection, evaluation and management on the cancer genetic counselor's time providing patient care.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 381, doi. 10.1007/s10689-011-9417-2

By:

Cohen, Stephanie;
McIlvried, Dawn

Publication type:

Article

A clinical perspective on genetic counseling and testing during end of life care for women with recurrent progressive ovarian cancer: opportunities and challenges.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 193, doi. 10.1007/s10689-011-9418-1

By:

Daniels, Molly;
Burzawa, Jennifer;
Brandt, Amanda;
Schmeler, Kathleen;
Lu, Karen

Publication type:

Article

Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 285, doi. 10.1007/s10689-011-9419-0

By:

Lastella, Patrizia;
Patruno, Margherita;
Forte, Giovanna;
Montanaro, Alba;
Gregorio, Carmela;
Sabbà, Carlo;
Suppressa, Patrizia;
Piepoli, Adalgisa;
Panza, Anna;
Andriulli, Angelo;
Resta, Nicoletta;
Stella, Alessandro

Publication type:

Article

Screening of 1331 Danish breast and/or ovarian cancer families identified 40 novel BRCA1 and BRCA2 mutations.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 207, doi. 10.1007/s10689-011-9422-5

By:

Hansen, Thomas;
Jønson, Lars;
Steffensen, Ane;
Andersen, Mette;
Kjaergaard, Susanne;
Gerdes, Anne-Marie;
Ejlertsen, Bent;
Nielsen, Finn

Publication type:

Article

Novel germline SDHD mutation: diagnosis and implications to the patient.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 365, doi. 10.1007/s10689-011-9421-6

By:

Varghese, Jeena;
Ayala-Ramirez, Montserrat;
Rich, Thereasa;
Rohren, Eric;
Rao, Priya;
Jimenez, Camilo

Publication type:

Article

Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: an observational descriptive study.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 199, doi. 10.1007/s10689-011-9420-7

By:

Yoon, Sook-Yee;
Thong, Meow-Keong;
Taib, Nur;
Yip, Cheng-Har;
Teo, Soo-Hwang

Publication type:

Article

Clinical characteristics and outcomes in familial adenomatous polyposis patients with a long-term treatment of celecoxib: a matched cohort study.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 303, doi. 10.1007/s10689-011-9423-4

By:

Huang, Kui;
Gutierrez, Lia;
Bülow, Steffen;
Gallinger, Steven;
Castells, Antoni;
Eagle, Craig;
Church, James

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

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

BRCA1/2 genetic testing uptake and psychosocial outcomes in men.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 213, doi. 10.1007/s10689-011-9425-2

By:

Graves, Kristi;
Gatammah, Rhoda;
Peshkin, Beth;
Krieger, Ayelet;
Gell, Christy;
Valdimarsdottir, Heiddis;
Schwartz, Marc

Publication type:

Article

A new phenotypic manifestation of familial adenomatous polyposis.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 309, doi. 10.1007/s10689-011-9432-3

By:

Edelstein, Daniel;
Giardiello, Francis;
Basiri, Ali;
Hylind, Linda;
Romans, Katharine;
Axilbund, Jennifer;
Cruz-Correa, Marcia;
Ramella-Roman, Jessica

Publication type:

Article

A novel de novo BRCA1 mutation in a Chinese woman with early onset breast cancer.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 233, doi. 10.1007/s10689-011-9429-y

By:

Kwong, Ava;
Ng, Enders;
Tang, Edmund;
Wong, Chris;
Law, Fian;
Leung, Candy;
Chan, Aaron;
Cheung, M.;
To, M.;
Ma, Edmond;
West, Dee;
Ford, James

Publication type:

Article

Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 397, doi. 10.1007/s10689-011-9428-z

By:

Lehtonen, Heli

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