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

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

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

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

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

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

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

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

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

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