Works matching IS 17312302 AND DT 2018 AND VI 16

Results: 17

Polyglobulia in patients with hemangioblastomas is related to tumor size but not to serum erythropoietin.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0097-x

By:

Krüger, Marie T.;
Klingler, Jan-Helge;
Jilg, Cordula;
Steiert, Christine;
Zschiedrich, Stefan;
Van Velthoven, Vera;
Gläsker, Sven

Publication type:

Article

German National Case Collection for familial pancreatic Cancer (FaPaCa) - acceptance and psychological aspects of a pancreatic cancer screening program.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0100-6

By:

Franke, Frederike S.;
Matthäi, Elvira;
Slater, Emily P.;
Schicker, Christoph;
Kruse, Johannes;
Bartsch, Detlef K.

Publication type:

Article

A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0098-9

By:

Karimi, Masoud;
von Salomé, Jenny;
Aravidis, Christos;
Silander, Gustav;
Askmalm, Marie Stenmark;
Henriksson, Isabelle;
Gebre-Medhin, Samuel;
Frödin, Jan-Erik;
Björck, Erik;
Lagerstedt-Robinson, Kristina;
Lindblom, Annika;
Tham, Emma

Publication type:

Article

CD36 – a plausible modifier of disease phenotype in familial adenomatous polyposis.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0096-y

By:

Holmes, Merran;
Connor, Toni;
Oldmeadow, Christopher;
Pockney, Peter G.;
Scott, Rodney J.;
Talseth-Palmer, Bente A.

Publication type:

Article

A qualitative study of barriers to genetic counseling and potential for mobile technology education among women with ovarian cancer.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0095-z

By:

Vogel, Rachel Isaksson;
Niendorf, Kristin;
Lee, Heewon;
Petzel, Sue;
Lee, Hee Yun;
Geller, Melissa A.

Publication type:

Article

High frequency of pathogenic non-founder germline mutations in <italic>BRCA1</italic> and <italic>BRCA2</italic> in families with breast and ovarian cancer in a founder population.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0094-0

By:

Maksimenko, J.;
Irmejs, A.;
Trofimovičs, G.;
Bērziņa, D.;
Skuja, E.;
Purkalne, G.;
Miklaševičs, E.;
Gardovskis, J.

Publication type:

Article

Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0090-4

By:

Schneider, Jennifer L.;
Goddard, Katrina A. B.;
Muessig, Kristin R.;
Davis, James V.;
Rope, Alan F.;
Hunter, Jessica E.;
Peterson, Susan K.;
Acheson, Louise S.;
Syngal, Sapna;
Wiesner, Georgia L.;
Reiss, Jacob A.

Publication type:

Article

Retraction Note to: The <italic>BRCA2</italic> variant c.68–7 T > A is associated with breast cancer.

Published in:

2018

By:

Møller, Pål;
Hovig, Eivind

Publication type:

Correction Notice

Clinical Genetics of Cancer 2017.

Published in:: 2018
Publication type:: Abstract

BRCA1 and BRCA2 mutation spectrum -- an update on mutation distribution in a large cancer genetics clinic in Norway.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-017-0085-6

By:

Heramb, Cecilie;
Wangensteen, Teresia;
Grindedal, Eli Marie;
Ariansen, Sarah Louise;
Lothe, Sheba;
Heimdal, Ketil Riddervold;
Mæhle, Lovise

Publication type:

Article

CDKN2A founder mutation in pancreatic ductal adenocarcinoma patients without cutaneous features of Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome.

Published in:

2018

By:

Cremin, Carol;
Howard, Sarah;
Le, Lyly;
Karsan, Aly;
Schaeffer, David F.;
Renouf, Daniel;
Schrader, Kasmintan A.

Publication type:

Case Study

Platinum-based neoadjuvant chemotherapy in BRCA1-positive breast cancer: a retrospective cohort analysis and literature review.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0092-2

By:

Sæther, Nikolai Havn;
Skuja, Elina;
Irmejs, Arvids;
Maksimenko, Jelena;
Miklasevics, Edvins;
Purkalne, Gunta;
Gardovskis, Janis

Publication type:

Article

Challenges in recruiting African-American women for a breast cancer genetics study.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, n. 1, p. N.PAG, doi. 10.1186/s13053-018-0091-3

By:

Compadre, Amanda J.;
Simonson, Melinda E.;
Gray, Katy;
Runnells, Gail;
Kadlubar, Susan;
Zorn, Kristin K.

Publication type:

Article

Central nervous system gadolinium accumulation in patients undergoing periodical contrast MRI screening for hereditary tumor syndromes.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-017-0084-7

By:

Vergauwen, Evelynn;
Vanbinst, Anne-Marie;
Brussaard, Carola;
Janssens, Peter;
De Clerck, Dieter;
Van Lint, Michel;
Houtman, Anne C.;
Michel, Olaf;
Keymolen, Kathelijn;
Lefevere, Bieke;
Bohler, Susanne;
Michielsen, Dirk;
Jansen, Anna C.;
Van Velthoven, Vera;
Gläsker, Sven

Publication type:

Article

Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-017-0083-8

By:

Gardner, Sabrina A.;
Weymouth, Katelyn S.;
Kelly, Wei S.;
Bogdanova, Ekaterina;
Chen, Wenjie;
Lupu, Daniel;
Suhl, Joshua;
Zeng, Qiandong;
Geigenmüller, Ute;
Boles, Debbie;
Okamoto, Patricia M.;
McDowell, Geraldine;
Hayden, Melissa A.;
Nagan, Narasimhan

Publication type:

Article

Frequency of <italic>BRCA1</italic> and <italic>BRCA2</italic> causative founder variants in ovarian cancer patients in South-East Poland.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-018-0089-x

By:

Kluz, Tomasz;
Jasiewicz, Andrzej;
Marczyk, Elżbieta;
Jach, Robert;
Jakubowska, Anna;
Lubiński, Jan;
Narod, Steven A.;
Gronwald, Jacek

Publication type:

Article

Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.

Published in:

Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-018-0086-0

By:

Dominguez-Valentin, Mev;
Evans, D. Gareth R.;
Nakken, Sigve;
Tubeuf, Hélène;
Vodak, Daniel;
Ekstrøm, Per Olaf;
Nissen, Anke M.;
Morak, Monika;
Holinski-Feder, Elke;
Martins, Alexandra;
Møller, Pål;
Hovig, Eivind

Publication type:

Article