Works matching IS 13899600 AND DT 2012 AND VI 11 AND IP 3

Results: 30

A prospective study of bowel preparation for colonoscopy with polyethylene glycol-electrolyte solution versus sodium phosphate in Lynch syndrome: a randomized trial.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 337, doi. 10.1007/s10689-012-9517-7

By:

Vugt van Pinxteren, Maria;
Kouwen, Mariëtte;
Oijen, Martijn;
Achterberg, Theo;
Nagengast, Fokko

Publication type:

Article

Common MUTYH mutations and colorectal cancer risk in multiethnic populations.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 329, doi. 10.1007/s10689-012-9516-8

By:

Lejbkowicz, Flavio;
Cohen, Ilana;
Barnett-Griness, Ofra;
Pinchev, Mila;
Poynter, Jen;
Gruber, Stephen;
Rennert, Gad

Publication type:

Article

Adequacy of family history taking in ovarian cancer patients: a population-based study.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 343, doi. 10.1007/s10689-012-9518-6

By:

Altena, Anne;
Aarle, Sandra;
Kiemeney, Lambertus;
Hoogerbrugge, Nicoline;
Massuger, Leon;
Hullu, Joanne

Publication type:

Article

Familial gastric cancer: guidelines for diagnosis, treatment and periodic surveillance.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 363, doi. 10.1007/s10689-012-9521-y

By:

Kluijt, Irma;
Sijmons, Rolf;
Hoogerbrugge, Nicoline;
Plukker, John;
Jong, Daphne;
Krieken, J.;
Hillegersberg, Richard;
Ligtenberg, Marjolijn;
Bleiker, Eveline;
Cats, Anemieke

Publication type:

Article

Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 351, doi. 10.1007/s10689-012-9519-5

By:

Brozek, Izabela;
Ratajska, Magdalena;
Piatkowska, Magdalena;
Kluska, Anna;
Balabas, Aneta;
Dabrowska, Michalina;
Nowakowska, Dorota;
Niwinska, Anna;
Rachtan, Jadwiga;
Steffen, Jan;
Limon, Janusz

Publication type:

Article

Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian families.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 519, doi. 10.1007/s10689-012-9515-9

By:

Tanyi, Miklós;
Olasz, Judit;
Tanyi, Janos;
Tóth, László;
Antal-Szalmás, Péter;
Bubán, Tamás;
András, Csilla;
Urbancsek, Hilda;
Garami, Zoltán;
Csuka, Orsolya;
Damjanovich, László

Publication type:

Article

Molecular characterization of parathyroid tumors from two patients with hereditary colorectal cancer syndromes.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 355, doi. 10.1007/s10689-012-9520-z

By:

Andreasson, Adam;
Sulaiman, Luqman;
Vale, Sónia;
Martins, João;
Ferreira, Florbela;
Miltenberger-Miltenyi, Gabriel;
Batista, Lucas;
Haglund, Felix;
Björck, Erik;
Nilsson, Inga-Lena;
Höög, Anders;
Larsson, Catharina;
Juhlin, C.

Publication type:

Article

The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees' outcome.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 371, doi. 10.1007/s10689-012-9522-x

By:

Platten, Ulla;
Rantala, Johanna;
Lindblom, Annika;
Brandberg, Yvonne;
Lindgren, Gunilla;
Arver, Brita

Publication type:

Article

The evolution of personalized cancer genetic counseling in the era of personalized medicine.

Published in:

2012

By:

Vig, Hetal;
Wang, Catharine

Publication type:

Letter

Nephron sparing surgery in von Hippel-Lindau associated renal cell carcinoma; clinicopathological long-term follow-up.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 387, doi. 10.1007/s10689-012-9525-7

By:

Jilg, C.;
Neumann, Hartmut;
Gläsker, S.;
Schäfer, O.;
Leiber, C.;
Ardelt, P.;
Schwardt, M.;
Schultze-Seemann, W.

Publication type:

Article

The consequences of risk reducing salpingo-oophorectomy: the case for a coordinated approach to long-term follow up post surgical menopause.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 403, doi. 10.1007/s10689-012-9527-5

By:

Pezaro, Carmel;
James, Paul;
McKinley, Joanne;
Shanahan, Mary;
Young, Mary-Anne;
Mitchell, Gillian

Publication type:

Article

Uroepithelial and kidney carcinoma in Lynch syndrome.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 395, doi. 10.1007/s10689-012-9526-6

By:

Aarnio, Markku;
Säily, Matti;
Juhola, Matti;
Gylling, Annette;
Peltomäki, Päivi;
Järvinen, Heikki;
Mecklin, Jukka-Pekka

Publication type:

Article

Mutation screening of RAD51C in high-risk breast and ovarian cancer families.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 381, doi. 10.1007/s10689-012-9523-9

By:

Lu, Wenping;
Wang, Xianshu;
Lin, Hongsheng;
Lindor, Noralane;
Couch, Fergus

Publication type:

Article

French experts report on MUTYH-associated polyposis (MAP).

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 321, doi. 10.1007/s10689-012-9511-0

By:

Buecher, Bruno;
Bonaïti, Catherine;
Buisine, Marie-Pierre;
Colas, Chrystelle;
Saurin, Jean-Christophe

Publication type:

Article

Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 411, doi. 10.1007/s10689-012-9529-3

By:

Ponti, Giovanni;
Pastorino, Lorenza;
Pollio, Annamaria;
Nasti, Sabina;
Pellacani, Giovanni;
Mignogna, Michele;
Tomasi, Aldo;
Del Forno, Corrado;
Longo, Caterina;
Bianchi-Scarrà, Giovanna;
Ficarra, Guido;
Seidenari, Stefania

Publication type:

Article

Breast cancer risk factors differ between Asian and white women with BRCA1/2 mutations.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 429, doi. 10.1007/s10689-012-9531-9

By:

Bruin, Monique;
Kwong, Ava;
Goldstein, Benjamin;
Lipson, Jafi;
Ikeda, Debra;
McPherson, Lisa;
Sharma, Bhavna;
Kardashian, Ani;
Schackmann, Elizabeth;
Kingham, Kerry;
Mills, Meredith;
West, Dee;
Ford, James;
Kurian, Allison

Publication type:

Article

Analysis of a Finnish family confirms RHBDF2 mutations as the underlying factor in tylosis with esophageal cancer.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 525, doi. 10.1007/s10689-012-9532-8

By:

Saarinen, Silva;
Vahteristo, Pia;
Lehtonen, Rainer;
Aittomäki, Kristiina;
Launonen, Virpi;
Kiviluoto, Tuula;
Aaltonen, Lauri

Publication type:

Article

A multidisciplinary clinic for individualizing management of patients at increased risk for breast and gynecologic cancer.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 419, doi. 10.1007/s10689-012-9530-x

By:

Engel, Natalie;
Gordon, Patricia;
Thull, Darcy;
Dudley, Beth;
Herstine, Judy;
Jankowitz, Rachel;
Zorn, Kristin

Publication type:

Article

The IL- 10 promoter haplotype and cancer risk: evidence from a meta-analysis.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 313, doi. 10.1007/s10689-012-9533-7

By:

Zhang, Kui;
Zhang, Lushun;
Wang, Xianmin;
Zhang, Lin

Publication type:

Article

Microsatellite instability testing in Korean patients with colorectal cancer.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 459, doi. 10.1007/s10689-012-9536-4

By:

Oh, Jung;
Kim, Duck-Woo;
Lee, Hye;
Lee, Hee;
Lee, Sung;
Jang, Je-Ho;
Kang, Sung-Bum;
Ku, Ja-Lok;
Jeong, Seung-Yong;
Park, Jae-Gahb

Publication type:

Article

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:

Familial Cancer, 2012, v. 11, n. 3, p. 449, doi. 10.1007/s10689-012-9535-5

By:

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

Publication type:

Article

Causes of death of mutation carriers in Finnish Lynch syndrome families.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 467, doi. 10.1007/s10689-012-9537-3

By:

Pylvänäinen, Kirsi;
Lehtinen, Tuula;
Kellokumpu, Ilmo;
Järvinen, Heikki;
Mecklin, Jukka-Pekka

Publication type:

Article

Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 483, doi. 10.1007/s10689-012-9540-8

By:

Catucci, Irene;
Milgrom, Roni;
Kushnir, Anya;
Laitman, Yael;
Paluch-Shimon, Shani;
Volorio, Sara;
Ficarazzi, Filomena;
Bernard, Loris;
Radice, Paolo;
Friedman, Eitan;
Peterlongo, Paolo

Publication type:

Article

Hepatoblastoma in two siblings and familial adenomatous polyposis: causal nexus or coincidence?

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 529, doi. 10.1007/s10689-012-9538-2

By:

Evers, Christina;
Gaspar, Harald;
Kloor, Matthias;
Bozukova, Gergana;
Kadmon, Martina;
Keller, Monika;
Sutter, Christian;
Moog, Ute

Publication type:

Article

Outcomes of a systems-level intervention offering breast cancer risk assessments to low-income underserved women.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 493, doi. 10.1007/s10689-012-9541-7

By:

Mays, Darren;
Sharff, McKane;
DeMarco, Tiffani;
Williams, Bernice;
Beck, Beth;
Sheppard, Vanessa;
Peshkin, Beth;
Eng-Wong, Jennifer;
Tercyak, Kenneth

Publication type:

Article

Breast and ovarian cancer risk management in a French cohort of 158 women carrying a BRCA1 or BRCA2 germline mutation: patient choices and outcome.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 473, doi. 10.1007/s10689-012-9539-1

By:

This, Pascale;
de la Rochefordière, Anne;
Savignoni, Alexia;
Falcou, Marie;
Tardivon, Anne;
Thibault, Fabienne;
Alran, Séverine;
Fourchotte, Virgine;
Fitoussi, Alfred;
Couturaud, Benoit;
Dolbeault, Sylvie;
Salmon, Remy;
Sigal-Zafrani, Brigitte;
Asselain, Bernard;
Stoppa-Lyonnet, Dominique

Publication type:

Article

Cancer spectrum in DNA mismatch repair gene mutation carriers: results from a hospital based Lynch syndrome registry.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 441, doi. 10.1007/s10689-012-9534-6

By:

Pande, Mala;
Wei, Chongjuan;
Chen, Jinyun;
Amos, Christopher;
Lynch, Patrick;
Lu, Karen;
Lucio, Laura;
Boyd-Rogers, Stephanie;
Bannon, Sarah;
Mork, Maureen;
Frazier, Marsha

Publication type:

Article

Novel germline c- MET mutation in a family with hereditary papillary renal carcinoma.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 535, doi. 10.1007/s10689-012-9542-6

By:

Wadt, Karin;
Gerdes, Anne-Marie;
Hansen, Thomas;
Toft, Birgitte;
Friis-Hansen, Lennart;
Andersen, Mette

Publication type:

Article

High prevalence of the c.1227_1228dup (p.Glu410GlyfsX43) mutation in Tunisian families affected with MUTYH-associated-polyposis.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 503, doi. 10.1007/s10689-012-9543-5

By:

Abdelmaksoud-Dammak, Rania;
Miladi-Abdennadher, Imen;
Amouri, Ali;
Tahri, Nabil;
Ayadi, Lobna;
Khabir, Abdelmajid;
Frikha, Foued;
Gargouri, Ali;
Mokdad-Gargouri, Raja

Publication type:

Article

Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome.

Published in:

Familial Cancer, 2012, v. 11, n. 3, p. 509, doi. 10.1007/s10689-012-9544-4

By:

Farrell, Michael;
Hughes, David;
Berry, Ian;
Gallagher, David;
Glogowski, Emily;
Payne, Stewart;
Kennedy, Michael;
Clarke, Róisín;
White, Susan;
Muldoon, Cian;
Macdonald, Fiona;
Rehal, Pauline;
Crompton, Danielle;
Roring, Solvig;
Duke, Sarah;
McDevitt, Trudi;
Barton, David;
Hodgson, Shirley;
Green, Andrew;
Daly, Peter

Publication type:

Article