Volume 13; Issue 2

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Familial Cancer
Volume 13; Issue 2

Familial Cancer

Volume 13; Issue 2

1

Barrett’s esophagus in the patients with familial adenomatous polyposis

Zoran Gatalica, Mingkui Chen, Carrie Snyder, Sumeet Mittal, Henry T. Lynch

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 186 KB

english, 2014

2

RAD51135G>C andTP53Arg72Pro polymorphisms and susceptibility to breast cancer in Serbian women

Krivokuca, Ana M., Malisic, Emina J., Dobricic, Jelena D., Brotto, Ksenija V., Cavic, Milena R., Jankovic, Radmila N., Tomasevic, Zorica I., Brankovic-Magic, Mirjana V.

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 256 KB

english, 2014

3

Inversion of exons 1–7 of theMSH2gene is a frequent cause of unexplained Lynch syndrome in one local population

Rhees, Jennifer, Arnold, Mildred, Boland, C. Richard

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 691 KB

english, 2014

4

Prevalence ofPALB2mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe

Noskowicz, Monika, Bogdanova, Natalia, Bermisheva, Marina, Takhirova, Zalina, Antonenkova, Natalia, Khusnutdinova, Elza, Bremer, Michael, Christiansen, Hans, Park-Simon, Tjoung-Won, Hillemanns, Peter,

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 274 KB

english, 2014

5

Breast cancer risk assessment in 8,824 women attending a family history evaluation and screening programme

Evans, D. Gareth R., Ingham, Sarah, Dawe, Sarah, Roberts, L., Lalloo, F., Brentnall, A. R., Stavrinos, P., Howell, Anthony

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 239 KB

english, 2014

6

Large genomic rearrangement ofBRCA1andBRCA2genes in familial breast cancer patients in Korea

Cho, Ja Young, Cho, Dae-Yeon, Ahn, Sei Hyun, Choi, Su-Youn, Shin, Inkyung, Park, Hyun Gyu, Lee, Jong Won, Kim, Hee Jeong, Yu, Jong Han, Ko, Beom Seok, Ku, Bo Kyung, Son, Byung Ho

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 1.10 MB

english, 2014

7

Potential genetic anticipation in hereditary leiomyomatosis-renal cell cancer (HLRCC)

Wong, Mei Hua, Tan, Chuen Seng, Lee, Soo Chin, Yong, Yvonne, Ooi, Aik Seng, Ngeow, Joanne, Tan, Min Han

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 471 KB

english, 2014

8

Deletion of exons 1–3 of theMEN1gene in a large Italian family causes the loss of menin expression

Zatelli, Maria Chiara, Tagliati, Federico, Ruvo, Mauro, Castermans, Emilie, Cavazzini, Luigi, Daly, Adrian F., Ambrosio, Maria Rosaria, Beckers, Albert, degli Uberti, Ettore

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 1.01 MB

english, 2014

9

Capsule endoscopy versus magnetic resonance enterography for the detection of small bowel polyps in Peutz–Jeghers syndrome

Urquhart, P., Grimpen, F., Lim, G. J., Pizzey, C., Stella, D. L., Tesar, P. A., Macrae, F. A., Appleyard, M. A., Brown, G. J.

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 1.74 MB

english, 2014

10

TheMUTYHhotspot mutations p.G396D and p.Y179C do not cause substantial genetic susceptibility to biliary cancer

Casper, M., Acalovschi, M., Lammert, F., Zimmer, V.

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 230 KB

english, 2014

11

Prophylactic total gastrectomy in hereditary diffuse gastric cancer: identification of two novelCDH1gene mutations—a clinical observational study

Bardram, Linda, Hansen, Thomas V. O., Gerdes, Anne-Marie, Timshel, Susanne, Friis-Hansen, Lennart, Federspiel, Birgitte

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 929 KB

english, 2014

12

Baseline and post prophylactic tubal–ovarian surgery CA125 levels inBRCA1andBRCA2mutation carriers

Chen, Ying, Bancroft, Elizabeth, Ashley, Sue, Arden-Jones, Audrey, Thomas, Sarah, Shanley, Susan, Saya, Sibel, Wakeling, Emma, Eeles, Rosalind

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 308 KB

english, 2014

13

Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation

Hasani-Ranjbar, Shirin, Rahmanian, Masoud, Ebrahim-Habibi, Azadeh, Soltani, Akbar, Soltanzade, Akbar, Mahrampour, Elnaz, Amoli, Mahsa M.

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 526 KB

english, 2014

14

A randomized controlled trial of diet and physical activity inBRCAmutation carriers

Pasanisi, P., Bruno, E., Manoukian, S., Berrino, F.

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 248 KB

english, 2014

15

Role of rapid sequence whole-body MRI screening inSDH-associated hereditary paraganglioma families

Jasperson, Kory W., Kohlmann, Wendy, Gammon, Amanda, Slack, Heidi, Buchmann, Luke, Hunt, Jason, Kirchhoff, Anne C., Baskin, Henry, Shaaban, Akram, Schiffman, Joshua D.

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 312 KB

english, 2014

16

Providing patient education: impact on quantity and quality of family health history collection

Chris A. Beadles,R. Ryanne Wu,Tiffany Himmel,Adam H. Buchanan…

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 484 KB

english, 2014

17

Comparison of attitudes regarding preimplantation genetic diagnosis among patients with hereditary cancer syndromes

Rich, Thereasa A., Liu, Mei, Etzel, Carol J., Bannon, Sarah A., Mork, Maureen E., Ready, Kaylene, Saraiya, Devki S., Grubbs, Elizabeth G., Perrier, Nancy D., Lu, Karen H., Arun, Banu K., Woodard, Terr

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 211 KB

english, 2014

18

More breast cancer patients preferBRCA-mutation testing without prior face-to-face genetic counseling

Sie, Aisha S., van Zelst-Stams, Wendy A. G., Spruijt, Liesbeth, Mensenkamp, Arjen R., Ligtenberg, Marjolijn J. L., Brunner, Han G., Prins, Judith B., Hoogerbrugge, Nicoline

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 292 KB

english, 2014

19

Misperceptions of ovarian cancer risk in women at increased risk for hereditary ovarian cancer

Meiser, Bettina, Price, Melanie A., Butow, Phyllis N., Rahman, Belinda, Tucker, Kathy, Cheah, Benjamin, Bickerstaffe, Adrian, Hopper, John, Phillips, Kelly-Anne

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 242 KB

english, 2014

20

Impact of familial risk and mammography screening on prognostic indicators of breast disease among women from the Ontario site of the Breast Cancer Family Registry

Walker, Meghan J., Mirea, Lucia, Cooper, Kristine, Nabavi, Mitra, Glendon, Gord, Andrulis, Irene L., Knight, Julia A., O’Malley, Frances P., Chiarelli, Anna M.

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 209 KB

english, 2014

21

Evaluation after five years of the cancer genetic counselling programme of Valencian Community (Eastern Spain)

Cuevas-Cuerda, Dolores, Salas-Trejo, Dolores

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 185 KB

english, 2014

22

Attitudes and knowledge of medical practitioners to hereditary cancer clinics and cancer genetic testing

Teng, Ian, Spigelman, Allan

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 2.31 MB

english, 2014

23

Is intraductal tubulopapillary neoplasia a new entity in the spectrum of familial pancreatic cancer syndrome?

Del Chiaro, Marco, Mucelli, Raffaella Pozzi, Blomberg, John, Segersvärd, Ralf, Verbeke, Caroline

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 466 KB

english, 2014

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