Works matching IS 13899600 AND DT 2019 AND VI 18 AND IP 2

Results: 20

Exploring the preferences of involved health professionals regarding the implementation of an online decision aid to support couples during reproductive decision-making in hereditary cancer: a mixed methods approach.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 285, doi. 10.1007/s10689-019-00119-7
By:
- Reumkens, Kelly;
- de Die-Smulders, Christine E. M.;
- van Osch, Liesbeth A. D. M.
Publication type:
Article
TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 273, doi. 10.1007/s10689-018-00118-0
By:
- Bakhuizen, J. J.;
- Hogervorst, F. B.;
- Velthuizen, M. E.;
- Ruijs, M. W.;
- van Engelen, K.;
- van Os, T. A.;
- Gille, J. J.;
- Collée, M.;
- van den Ouweland, A. M.;
- van Asperen, C. J.;
- Kets, C. M.;
- Mensenkamp, A. R.;
- Leter, E. M.;
- Blok, M. J.;
- de Jong, M. M.;
- Ausems, M. G.
Publication type:
Article
Recent advances in Lynch syndrome.
Published in:
2019
By:
- Biller, Leah H.;
- Syngal, Sapna;
- Yurgelun, Matthew B.
Publication type:
Letter
Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 203, doi. 10.1007/s10689-018-00116-2
By:
- Sutcliffe, Erin G.;
- Bartenbaker Thompson, Amanda;
- Stettner, Amy R.;
- Marshall, Megan L.;
- Roberts, Maegan E.;
- Susswein, Lisa R.;
- Wang, Ying;
- Klein, Rachel T.;
- Hruska, Kathleen S.;
- Solomon, Benjamin D.
Publication type:
Article
Progress report on the major clinical advances in patient-oriented research into familial melanoma (2013–2018).
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 267, doi. 10.1007/s10689-018-00115-3
By:
- Visser, Mijke;
- van der Stoep, Nienke;
- Gruis, Nelleke
Publication type:
Article
Monoallelic MUTYH carrier status is not associated with increased breast cancer risk in a multigene panel cohort.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 197, doi. 10.1007/s10689-018-00114-4
By:
- Fulk, Kelly;
- LaDuca, Holly;
- Black, Mary Helen;
- Qian, Dajun;
- Tian, Yuan;
- Yussuf, Amal;
- Espenschied, Carin;
- Jasperson, Kory
Publication type:
Article
A squamous cell carcinoma in a young woman with Lynch syndrome.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 193, doi. 10.1007/s10689-018-00113-5
By:
- Adan, F.;
- Crijns, M. B.;
- Dekker, E.;
- Bastiaansen, B. A. J.;
- Lapid, O.;
- Snaebjornsson, P.;
- Rosenberg, E. H.;
- van Leerdam, M. E.;
- Bekkenk, M. W.
Publication type:
Article
Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 261, doi. 10.1007/s10689-018-0112-4
By:
- Baig, Shahid Mahmood;
- Fatima, Ambrin;
- Tariq, Muhammad;
- Khan, Tahir Naeem;
- Ali, Zafar;
- Faheem, Mohammad;
- Mahmood, Humera;
- Killela, Patrick;
- Waitkus, Matthew;
- He, Yiping;
- Zhao, Fangping;
- Wang, Sizhen;
- Jiao, Yuchen;
- Yan, Hai
Publication type:
Article
Cleft lip/palate and hereditary diffuse gastric cancer: report of a family harboring a CDH1 c.687 + 1G > A germline mutation and review of the literature.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 253, doi. 10.1007/s10689-018-0111-5
By:
- Obermair, Florian;
- Rammer, Melanie;
- Burghofer, Jonathan;
- Malli, Theodora;
- Schossig, Anna;
- Wimmer, Katharina;
- Kranewitter, Wolfgang;
- Mayrbaeurl, Beate;
- Duba, Hans-Christoph;
- Webersinke, Gerald
Publication type:
Article
Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 281, doi. 10.1007/s10689-018-0110-6
By:
- Vos, Janet R.;
- Giepmans, Lisette;
- Röhl, Claas;
- Geverink, Nicoline;
- Hoogerbrugge, Nicoline
Publication type:
Article
Risk of multiple colorectal cancer development depends on age and subgroup in individuals with hereditary predisposition.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 183, doi. 10.1007/s10689-018-0109-z
By:
- Lindberg, Lars J.;
- Wegen-Haitsma, Wia;
- Ladelund, Steen;
- Smith-Hansen, Lars;
- Therkildsen, Christina;
- Bernstein, Inge;
- Nilbert, Mef
Publication type:
Article
Ovarian small cell carcinoma in one of a pair of monozygous twins.
Published in:
2019
By:
- Fahiminiya, Somayyeh;
- Sabbaghian, Nelly;
- Albrecht, Steffen;
- Nadaf, Javad;
- Callegaro-Filho, Donato;
- Foulkes, William D.
Publication type:
Letter
NTHL1-associate polyposis: first Australian case report.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 179, doi. 10.1007/s10689-018-0107-1
By:
- Groves, Alexandra;
- Gleeson, Margaret;
- Spigelman, Allan D.
Publication type:
Article
Referral frequency, attrition rate, and outcomes of germline testing in patients with pancreatic adenocarcinoma.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 241, doi. 10.1007/s10689-018-0106-2
By:
- Walker, Evan J.;
- Carnevale, Julia;
- Pedley, Christina;
- Blanco, Amie;
- Chan, Salina;
- Collisson, Eric A.;
- Tempero, Margaret A.;
- Ko, Andrew H.
Publication type:
Article
Electronically ascertained extended pedigrees in breast cancer genetic counseling.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 153, doi. 10.1007/s10689-018-0105-3
By:
- Stefansdottir, V.;
- Skirton, H.;
- Johannsson, O. Th.;
- Olafsdottir, H.;
- Olafsdottir, G. H.;
- Tryggvadottir, L.;
- Jonsson, J. J.
Publication type:
Article
Development and pilot testing of a leaflet informing women with breast cancer about genomic testing for polygenic risk.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 147, doi. 10.1007/s10689-018-0104-4
By:
- Kaur, Rajneesh;
- Meiser, Bettina;
- Yanes, Tatiane;
- Young, Mary-Anne;
- Barlow-Stewart, Kristine;
- Roscioli, Tony;
- Smith, Sian;
- James, Paul A.
Publication type:
Article
Genetic counselling of young women with breast cancer for Li–Fraumeni syndrome: a nationwide survey on the experiences and attitudes of genetics professionals.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 231, doi. 10.1007/s10689-018-0103-5
By:
- Bakhuizen, J. J.;
- Velthuizen, M. E.;
- Stehouwer, S.;
- Bleiker, E. M.;
- Ausems, M. G.
Publication type:
Article
Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 173, doi. 10.1007/s10689-018-0102-6
By:
- Vande Perre, P.;
- Siegfried, A.;
- Corsini, C.;
- Bonnet, D.;
- Toulas, C.;
- Hamzaoui, N.;
- Selves, J.;
- Chipoulet, E.;
- Hoffmann, J. S.;
- Uro-Coste, E.;
- Guimbaud, R.
Publication type:
Article
Interest in, willingness-to-pay for and willingness-to-recommend genetic testing for prostate cancer among affected men after radical prostatectomy.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 221, doi. 10.1007/s10689-018-0101-7
By:
- Mayer, Marcel;
- Selig, Katharina;
- Tüttelmann, Frank;
- Dinkel, Andreas;
- Gschwend, Jürgen E.;
- Herkommer, Kathleen
Publication type:
Article
Massive juvenile polyposis of the stomach in a family with SMAD4 gene mutation.
Published in:
Familial Cancer, 2019, v. 18, n. 2, p. 165, doi. 10.1007/s10689-018-0100-8
By:
- de Leon, Maurizio Ponz;
- Pedroni, Monica;
- Viel, Alessandra;
- Luppi, Claudio;
- Conigliaro, Rita;
- Domati, Federica;
- Rossi, Giuseppina;
- Bonetti, Luca Reggiani
Publication type:
Article