Works matching IS 17312302 AND DT 2013 AND VI 11 AND IP 1

Results: 15

Hereditary cancer risk assessment: essential tools for a better approach.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 39, doi. 10.1186/1897-4287-11-16

By:

Gomy, Israel;
Estevez, Maria Del Pilar

Publication type:

Article

Familial adenomatous polyposis of the colon.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 21, doi. 10.1186/1897-4287-11-15

By:

Plawski, Andrzej;
Banasiewicz, Tomasz;
Borun, Pawel;
Kubaszewski, Lukasz;
Krokowicz, Piotr;
Skrzypczak-Zielinska, Marzena;
Lubinski, Jan

Publication type:

Article

Experience of BRCA1/2 mutation-negative young women from families with hereditary breast and ovarian cancer: a qualitative study.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-14

By:

Macrae, Lynn;
Navarro de Souza, Alicia;
Loiselle, Carmen G.;
Wong, Nora

Publication type:

Article

Hereditary breast cancer: ever more pieces to the polygenic puzzle.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-12

By:

Bogdanova, Natalia;
Helbig, Sonja;
Dörk, Thilo

Publication type:

Article

Acute myeloid leukemia in a 38-year-old hemodialyzed patient with von Hippel-Lindau disease.

Published in:

2013

By:

Labno-Kirszniok, Katarzyna;
Nieszporek, Teresa;
Wiecek, Andrzej;
Helbig, Grzegorz;
Lubinski, Jan

Publication type:

Case Study

Germline deletions in the EPCAM gene as a cause of Lynch syndrome - literature review.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-9

By:

Tutlewska, Katarzyna;
Lubinski, Jan;
Kurzawski, Grzegorz

Publication type:

Article

Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome.

Published in:

2013

By:

Paparo, Lorella;
Rossi, Giovanni Battista;
Delrio, Paolo;
Rega, Daniela;
Duraturo, Francesca;
Liccardo, Raffaella;
Debellis, Mario;
Izzo, Paola;
Rosa, Marina De

Publication type:

Case Study

Comparison of whole genome amplification and nested-PCR methods for preimplantation genetic diagnosis for BRCA1 gene mutation on unfertilized oocytes-a pilot study.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-10

By:

Michalska, Danuta;
Jaguszewska, Kinga;
Liss, Joanna;
Kitowska, Kamila;
Mirecka, Agata;
Łukaszuk, Krzysztof

Publication type:

Article

Sense of coherence and self-concept in Lynch syndrome.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-7

By:

Petersen, Helle Vendel;
Ladelund, Steen;
Carlsson, Christina;
Nilbert, Mef

Publication type:

Article

Optimizing recruitment to a prostate cancer surveillance program among male BRCA1 mutation carriers: invitation by mail or by telephone.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-17

By:

Galor, Anna;
Cybulski, Cezary;
Lubinski, Jan;
Narod, Steven A.;
Gronwald, Jacek

Publication type:

Article

Carcinogenesis of PIK3CA.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-5

By:

German, Sidra;
Aslam, Hafiz Muhammad;
Saleem, Shafaq;
Raees, Aisha;
Anum, Tooba;
Alvi, Arsalan Ahmad;
Haseeb, Abdul

Publication type:

Article

The impact of genetic variants in inflammatory-related genes on prostate cancer risk among men of African Descent: a case control study.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-19

By:

Jones, Dominique Z.;
Ragin, Camille;
Kidd, Nayla C.;
Flores-Obando, Rafael E.;
Jackson, Maria;
McFarlane-Anderson, Norma;
Tulloch-Reid, Marshall;
Kimbro, Kevin S.;
Kidd, LaCreis R.

Publication type:

Article

Psoriasis vulgaris and familial cancer riska population-based study.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-6

By:

Maleszka, Romuald;
Paszkowska-Szczur, Katarzyna;
Soczawa, Ewa;
Boer, Magdalena;
Różewicka-Czabańska, Monika;
Wiśniewska, Joanna;
Mirecka, Aneta;
Krysztoforska, Lidia;
Adamski, Zygmunt;
Lubinski, Jan;
Dębniak, Tadeusz

Publication type:

Article

The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-20

By:

Talseth-Palmer, Bente A.;
Wijnen, Juul T.;
Andreassen, Eva K.;
Barker, Daniel;
Jagmohan-Changur, Shantie;
Tops, Carli M.;
Meldrum, Cliff;
Spigelman, Allan;
Hes, Frederik J.;
Van Wezel, Tom;
Vasen, Hans F. A.;
Scott, Rodney J.

Publication type:

Article

Mutation spectrum in South American Lynch syndrome families.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-18

By:

Dominguez-Valentin, Mev;
Nilbert, Mef;
Wernhoff, Patrik;
López-Köstner, Francisco;
Vaccaro, Carlos;
Sarroca, Carlos;
Ines Palmero, Edenir;
Giraldo, Alejandro;
Ashton-Prolla, Patricia;
Alvarez, Karin;
Ferro, Alejandra;
Neffa, Florencia;
Caris, Junea;
Carraro, Dirce M.;
Rossi, Benedito M.

Publication type:

Article