Works matching IS 13899600 AND DT 2015 AND VI 14 AND IP 4

Results: 21

Birt-Hogg-Dubé syndrome and intracranial vascular pathologies.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 595, doi. 10.1007/s10689-015-9807-y

By:

Kapoor, Rahul;
Evins, Alexander;
Steitieh, Diala;
Bernardo, Antonio;
Stieg, Philip

Publication type:

Article

Prevalence and detection of psychosocial problems in cancer genetic counseling.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 629, doi. 10.1007/s10689-015-9809-9

By:

Eijzenga, W.;
Bleiker, E.;
Hahn, D.;
Kolk, L.;
Sidharta, G.;
Aaronson, N.

Publication type:

Article

Childhood cancers in families with and without Lynch syndrome.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 545, doi. 10.1007/s10689-015-9810-3

By:

Heath, John;
Reece, Jeanette;
Buchanan, Daniel;
Casey, Graham;
Durno, Carol;
Gallinger, Steven;
Haile, Robert;
Newcomb, Polly;
Potter, John;
Thibodeau, Stephen;
Le Marchand, Loïc;
Lindor, Noralane;
Hopper, John;
Jenkins, Mark;
Win, Aung

Publication type:

Article

Psychological distress related to BRCA testing in ovarian cancer patients.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 495, doi. 10.1007/s10689-015-9811-2

By:

Bjørnslett, Merete;
Dahl, Alv;
Sørebø, Øystein;
Dørum, Anne

Publication type:

Article

Survival in familial colorectal cancer: a Danish cohort study.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 553, doi. 10.1007/s10689-015-9812-1

By:

Lautrup, Charlotte;
Mikkelsen, Ellen;
Lash, Timothy;
Katballe, Niels;
Sunde, Lone

Publication type:

Article

A functional HOTAIR rs920778 polymorphism does not contributes to gastric cancer in a Turkish population: a case-control study.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 561, doi. 10.1007/s10689-015-9813-0

By:

Bayram, Süleyman;
Ülger, Yakup;
Sümbül, Ahmet;
Kaya, Berrin;
Rencüzoğulları, Ahmet;
Genç, Ahmet;
Sevgiler, Yusuf;
Bozkurt, Onur;
Rencüzoğulları, Eyyüp

Publication type:

Article

BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 505, doi. 10.1007/s10689-015-9814-z

By:

de Juan, Inmaculada;
Palanca, Sarai;
Domenech, Asunción;
Feliubadaló, Lidia;
Segura, Ángel;
Osorio, Ana;
Chirivella, Isabel;
de la Hoya, Miguel;
Sánchez, Ana;
Infante, Mar;
Tena, Isabel;
Díez, Orland;
Garcia-Casado, Zaida;
Vega, Ana;
Teulé, Àlex;
Barroso, Alicia;
Pérez, Pedro;
Durán, Mercedes;
Carrasco, Estela;
Juan-Fita, Mª

Publication type:

Article

Supporting families with Cancer: A patient centred survivorship model of care.

Published in:

2015

By:

Craft, Emily;
Billington, Caron;
O'Sullivan, Rory;
Watson, Wendy;
Suter-Giorgini, Nicola;
Singletary, Joanne;
King, Elizabeth;
Perfirgines, Matthew;
Cashmore, Annette;
Barwell, Julian

Publication type:

Letter

Follicular variant of papillary thyroid cancer in Alström syndrome.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 599, doi. 10.1007/s10689-015-9816-x

By:

Papadakis, M.;
Meyer, A.;
Schuster, F.;
Weyerbrock, N.;
Corinth, C.;
Dotzenrath, C.

Publication type:

Article

Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 641, doi. 10.1007/s10689-015-9817-9

By:

Marcus, Rebecca;
Geurts, Jennifer;
Grzybowski, Jessica;
Turaga, Kiran;
Clark Gamblin, T.;
Strong, Kimberly;
Johnston, Fabian

Publication type:

Article

Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 603, doi. 10.1007/s10689-015-9818-8

By:

Bugalho, Maria;
Silva, Ana;
Domingues, Rita

Publication type:

Article

BRCA1 gene variant p.P142H associated with male breast cancer: a two-generation genealogic study and literature review.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 515, doi. 10.1007/s10689-015-9819-7

By:

Spinelli, Claudio;
Strambi, Silvia;
Piccini, Lorenzo;
Rossi, Leonardo;
Aretini, Paolo;
Caligo, Adelaide

Publication type:

Article

High accuracy of family history of melanoma in Danish melanoma cases.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 609, doi. 10.1007/s10689-015-9820-1

By:

Wadt, Karin;
Drzewiecki, Krzysztof;
Gerdes, Anne-Marie

Publication type:

Article

Metastatic sympathetic paraganglioma in a patient with loss of the SDHC gene.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 615, doi. 10.1007/s10689-015-9821-0

By:

Rich, Thereasa;
Jackson, Michelle;
Roman-Gonzalez, Alejandro;
Shah, Komal;
Cote, Gilbert;
Jimenez, Camilo

Publication type:

Article

Massive gastric polyposis associated with a germline SMAD4 gene mutation.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 569, doi. 10.1007/s10689-015-9822-z

By:

Soer, Eline;
Vos tot Nederveen Cappel, Wouter;
Ligtenberg, Marjolijn;
Moll, Freek;
Pierik, Robert;
Vecht, Juda;
Vasen, Hans;
Flierman, Antoine

Publication type:

Article

Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UK.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 521, doi. 10.1007/s10689-015-9823-y

By:

Chandrasekaran, Dhivya;
Menon, Usha;
Evans, Gareth;
Crawford, Robin;
Saridogan, Ertan;
Jacobs, Chris;
Tischkowitz, Marc;
Brockbank, Elly;
Kalsi, Jatinder;
Jurkovic, Davor;
Manchanda, Ranjit

Publication type:

Article

Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 575, doi. 10.1007/s10689-015-9824-x

By:

Win, Aung;
Reece, Jeanette;
Buchanan, Daniel;
Clendenning, Mark;
Young, Joanne;
Cleary, Sean;
Kim, Hyeja;
Cotterchio, Michelle;
Dowty, James;
MacInnis, Robert;
Tucker, Katherine;
Winship, Ingrid;
Macrae, Finlay;
Burnett, Terrilea;
Le Marchand, Loïc;
Casey, Graham;
Haile, Robert;
Newcomb, Polly;
Thibodeau, Stephen;
Lindor, Noralane

Publication type:

Article

Risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a 30-year semi-prospective analysis.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 531, doi. 10.1007/s10689-015-9825-9

By:

Basu, N.;
Ingham, S.;
Hodson, J.;
Lalloo, F.;
Bulman, M.;
Howell, A.;
Evans, D.

Publication type:

Article

POLE mutations in families predisposed to cutaneous melanoma.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 621, doi. 10.1007/s10689-015-9826-8

By:

Aoude, Lauren;
Heitzer, Ellen;
Johansson, Peter;
Gartside, Michael;
Wadt, Karin;
Pritchard, Antonia;
Palmer, Jane;
Symmons, Judith;
Gerdes, Anne-Marie;
Montgomery, Grant;
Martin, Nicholas;
Tomlinson, Ian;
Kearsey, Stephen;
Hayward, Nicholas

Publication type:

Article

The effect of personal medical history and family history of cancer on the uptake of risk-reducing salpingo-oophorectomy.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 539, doi. 10.1007/s10689-015-9827-7

By:

Aa, Jessica;
Hoogendam, Jacob;
Butter, Els;
Ausems, Margreet;
Verheijen, René;
Zweemer, Ronald

Publication type:

Article

Genotype-phenotype analysis of von Hippel-Lindau syndrome in fifteen Indian families.

Published in:

Familial Cancer, 2015, v. 14, n. 4, p. 585, doi. 10.1007/s10689-015-9806-z

By:

Vikkath, Narendranath;
Valiyaveedan, Sindhu;
Nampoothiri, Sheela;
Radhakrishnan, Natasha;
Pillai, Gopal;
Nair, Vasantha;
Pooleri, Ginil;
Mathew, Georgie;
Menon, Krishnakumar;
Ariyannur, Prasanth;
Pillai, Ashok

Publication type:

Article