Works matching IS 13899600 AND DT 2010 AND VI 9 AND IP 3

Results: 33

Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 297, doi. 10.1007/s10689-009-9313-1

By:

Sanz, Judit;
Ramón y Cajal, Teresa;
Torres, Asunción;
Darder, Esther;
Gadea, Neus;
Velasco, Angela;
Fortuny, Daniel;
López, Consol;
Fisas, David;
Brunet, Joan;
Alonso, M.;
Balmaña, Judith

Publication type:

Article

Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndrome.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 345, doi. 10.1007/s10689-009-9314-0

By:

Kwok, Chau-To;
Ward, Robyn;
Hawkins, Nicholas;
Hitchins, Megan

Publication type:

Article

Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 283, doi. 10.1007/s10689-010-9345-6

By:

Steffensen, Ane;
Jønson, Lars;
Ejlertsen, Bent;
Gerdes, Anne-Marie;
Nielsen, Finn;
Hansen, Thomas

Publication type:

Article

Location in the large bowel influences the APC mutations observed in FAP adenomas.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 389, doi. 10.1007/s10689-010-9332-y

By:

Will, O.;
Leedham, S.;
Elia, G.;
Phillips, R.;
Clark, S.;
Tomlinson, I.

Publication type:

Article

Pregnancy after prophylactic total gastrectomy.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 331, doi. 10.1007/s10689-009-9316-y

By:

Kaurah, Pardeep;
Fitzgerald, Rebecca;
Dwerryhouse, Sarah;
Huntsman, David

Publication type:

Article

Update multiple endocrine neoplasia type 2.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 449, doi. 10.1007/s10689-010-9320-2

By:

Raue, Friedhelm;
Frank-Raue, Karin

Publication type:

Article

“ I have always believed I was at high risk...” The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of free-text questionnaire comments.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 469, doi. 10.1007/s10689-010-9324-y

By:

Hilgart, J.;
Phelps, C.;
Bennett, P.;
Hood, K.;
Brain, K.;
Murray, A.

Publication type:

Article

High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 383, doi. 10.1007/s10689-010-9321-1

By:

Nyiraneza, Christine;
Marbaix, Etienne;
Smets, Mireille;
Galant, Christine;
Sempoux, Christine;
Dahan, Karin

Publication type:

Article

Carney triad versus Carney Stratakis syndrome: two cases which illustrate the difficulty in distinguishing between these conditions in individual patients.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 443, doi. 10.1007/s10689-010-9323-z

By:

Alrashdi, Ismail;
Bano, Gul;
Maher, Eamonn;
Hodgson, Shirley

Publication type:

Article

Assessment of clinical practices among cancer genetic counselors.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 459, doi. 10.1007/s10689-010-9326-9

By:

Wham, Deborah;
Vu, Thuy;
Chan-Smutko, Gayun;
Kobelka, Christine;
Urbauer, Diana;
Heald, Brandie

Publication type:

Article

Can self-esteem, mastery and perceived stigma predict long-term adjustment in women carrying a BRCA1/2-mutation? Evidence from a multi-center study.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 305, doi. 10.1007/s10689-010-9325-x

By:

Vodermaier, Andrea;
Esplen, Mary;
Maheu, Christine

Publication type:

Article

Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 291, doi. 10.1007/s10689-010-9327-8

By:

Esteban Cardeñosa, Eva;
Bolufer Gilabert, Pascual;
Juan Jiménez, Inmaculada;
Palanca Suela, Sarai;
Barragán González, Eva;
González Anguix, Virginia;
Lerma Alejos, Enrique;
Chirivella González, Isabel;
Segura Huerta, Ángel;
Guillén Ponce, Carmen;
Martínez de Dueñas, Eduardo;
Cuevas Cuerda, Dolores;
Salas Trejo, Dolores

Publication type:

Article

RASSF1A polymorphism in familial breast cancer.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 263, doi. 10.1007/s10689-010-9335-8

By:

Bergqvist, J.;
Latif, A.;
Roberts, S.;
Hadfield, K.;
Lalloo, F.;
Howell, A.;
Evans, D.;
Newman, W.

Publication type:

Article

Analysis of mismatch repair gene mutations in Turkish HNPCC patients.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 365, doi. 10.1007/s10689-010-9336-7

By:

Tunca, Berrin;
Pedroni, Monica;
Cecener, Gulsah;
Egeli, Unal;
Borsi, Enrica;
Zorluoglu, Abdullah;
Gregorio, Carmela;
Yilmazlar, Tuncay;
Yerci, Omer;
Leon, Maurizio

Publication type:

Article

Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 267, doi. 10.1007/s10689-010-9338-5

By:

Balabas, Aneta;
Skasko, Elzbieta;
Nowakowska, Dorota;
Niwinska, Anna;
Blecharz, Pawel

Publication type:

Article

Atypical identification of Lynch syndrome by immunohistochemistry and microsatellite instability analysis on jejunal adenocarcinoma.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 377, doi. 10.1007/s10689-010-9339-4

By:

McIlvried, D.;
Birhiray, R.;
Lu, J.

Publication type:

Article

Differences in clinical and pathological characteristics of colorectal cancer in Arab as compared to Jewish patients in Northern Israel.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 327, doi. 10.1007/s10689-010-9337-6

By:

Glushko, Yelena;
Basher, Walid;
Barchana, Micha;
Zidan, Jamal

Publication type:

Article

Novel one-stop multidisciplinary follow-up clinic significantly improves cancer risk management in BRCA1/2 carriers.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 313, doi. 10.1007/s10689-010-9333-x

By:

Pichert, G.;
Jacobs, C.;
Jacobs, I.;
Menon, U.;
Manchanda, R.;
Johnson, M.;
Hamed, H.;
Firth, C.;
Evison, M.;
Tutt, A.;
Silva, L.;
Langman, C.;
Izatt, L.

Publication type:

Article

Lynch syndrome: the influence of environmental factors on extracolonic cancer risk in hMLH1 c.C1528T mutation carriers and their mutation-negative sisters.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 357, doi. 10.1007/s10689-010-9334-9

By:

Blokhuis, M.;
Pietersen, G.;
Goldberg, P.;
Algar, U.;
Merwe, L.;
Mbatani, N.;
Vorster, A.;
Ramesar, R.

Publication type:

Article

A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 395, doi. 10.1007/s10689-009-9317-x

By:

Fostira, Florentia;
Yannoukakos, Drakoulis

Publication type:

Article

Prevalence of BRCA2 and CDKN2a mutations in German familial pancreatic cancer families.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 335, doi. 10.1007/s10689-010-9329-6

By:

Slater, Emily;
Langer, Peter;
Fendrich, Volker;
Habbe, Nils;
Chaloupka, Brunhilde;
Matthäi, Elvira;
Sina, Mercedes;
Hahn, Stephan;
Bartsch, Detlef

Publication type:

Article

Identification of the first case of germline duplication of BRCA1 exon 13 in an Italian family.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 275, doi. 10.1007/s10689-009-9315-z

By:

Cerutti, Roberta;
Sahnane, Nora;
Carnevali, Ileana;
Furlan, Daniela;
Tibiletti, Maria;
Chiaravalli, Anna;
Capella, Carlo

Publication type:

Article

LOH analysis should not be used as a tool to assess whether UVs of BRCA1/2 are pathogenic or not.

Published in:

2010

By:

Beristain, E.;
Guerra, I.;
Vidaurrazaga, N.;
Burgos-Bretones, J.;
Tejada, M.

Publication type:

Letter

A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 425, doi. 10.1007/s10689-009-9319-8

By:

Abbaszadeh, Fatemeh;
Barker, Karen;
McConville, Carmel;
Scott, Richard;
Rahman, Nazneen

Publication type:

Article

Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 431, doi. 10.1007/s10689-010-9328-7

By:

Abdel-Rahman, M.;
Pilarski, R.;
Ezzat, S.;
Sexton, J.;
Davidorf, F.

Publication type:

Article

Successful oxytocin-assisted nipple aspiration in women at increased risk for breast cancer.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 321, doi. 10.1007/s10689-010-9344-7

By:

Suijkerbuijk, Karijn;
Wall, Elsken;
Meijrink, Helen;
Pan, Xiaojuan;
Borel Rinkes, Inne;
Ausems, Margreet;
Diest, Paul

Publication type:

Article

Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 401, doi. 10.1007/s10689-010-9331-z

By:

Klockars, Tuomas;
Renkonen, Suvi;
Leivo, Ilmo;
Hagström, Jaana;
Mäkitie, Antti

Publication type:

Article

Erratum to: Survey of familial glioma and role of germline p16 INK4A/ p14 ARF and p53 mutation.

Published in:

2010

By:

Robertson, Lindsay;
Armstrong, Georgina;
Olver, Bianca;
Lloyd, Amy;
Shete, Sanjay;
Lau, Ching;
Claus, Elizabeth;
Barnholtz-Sloan, Jill;
Lai, Rose;
Il’yasova, Dora;
Schildkraut, Joellen;
Bernstein, Jonine;
Olson, Sara;
Jenkins, Robert;
Yang, Ping;
Rynearson, Amanda;
Wrensch, Margaret;
McCoy, Lucie;
Wienkce, John;
McCarthy, Bridget

Publication type:

Correction Notice

Survey of familial glioma and role of germline p16 INK4A /p14 ARF and p53 mutation.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 413, doi. 10.1007/s10689-010-9346-5

By:

Robertson, Lindsay;
Armstrong, Georgina;
Olver, Bianca;
Lloyd, Amy;
Shete, Sanjay;
Lau, Ching;
Claus, Elizabeth;
Barnholtz-Sloan, Jill;
Lai, Rose;
Il’yasova, Dora;
Schildkraut, Joellen;
Bernstein, Jonine;
Olson, Sara;
Jenkins, Robert;
Yang, Ping;
Rynerason, Amanda;
Wrensch, Margaret;
McCoy, Lucie;
Wienkce, John;
McCarthy, Bridget

Publication type:

Article

Screening for germline DND1 mutations in testicular cancer patients.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 439, doi. 10.1007/s10689-010-9340-y

By:

Sijmons, Rolf;
Vos, Yvonne;
Herkert, Johanna;
Bos, Krista;
Holzik, Martijn;
Hoekstra-Weebers, Josette;
Hofstra, Robert;
Hoekstra, Harald

Publication type:

Article

Familial adenomatous polyposis (FAP) and gender. Does gender influence the genetic transmission of FAP?

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 405, doi. 10.1007/s10689-010-9341-x

By:

Farinella, Eriberto;
Soobrah, Ramawad;
Phillips, Robin;
Clark, Susan

Publication type:

Article

Surgical prophylaxis in familial adenomatous polyposis: do pre-existing desmoids outside the abdominal cavity matter?

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 407, doi. 10.1007/s10689-010-9342-9

By:

Sinha, Ashish;
Gibbons, Daniel;
Phillips, Robin;
Clark, Sue

Publication type:

Article

Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 479, doi. 10.1007/s10689-010-9343-8

By:

Brandt, Amanda;
Tschirgi, Matthew;
Ready, Kaylene;
Sun, Charlotte;
Darilek, Sandra;
Hecht, Jacqueline;
Arun, Banu;
Lu, Karen

Publication type:

Article

Works matching IS 13899600 AND DT 2010 AND VI 9 AND IP 3

Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain.

Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndrome.

Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations.

Location in the large bowel influences the APC mutations observed in FAP adenomas.

Pregnancy after prophylactic total gastrectomy.

Update multiple endocrine neoplasia type 2.

“ I have always believed I was at high risk...” The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of free-text questionnaire comments.

High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome.

Carney triad versus Carney Stratakis syndrome: two cases which illustrate the difficulty in distinguishing between these conditions in individual patients.

Assessment of clinical practices among cancer genetic counselors.

Can self-esteem, mastery and perceived stigma predict long-term adjustment in women carrying a BRCA1/2-mutation? Evidence from a multi-center study.

Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence.

RASSF1A polymorphism in familial breast cancer.

Analysis of mismatch repair gene mutations in Turkish HNPCC patients.

Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland.

Atypical identification of Lynch syndrome by immunohistochemistry and microsatellite instability analysis on jejunal adenocarcinoma.

Differences in clinical and pathological characteristics of colorectal cancer in Arab as compared to Jewish patients in Northern Israel.

Novel one-stop multidisciplinary follow-up clinic significantly improves cancer risk management in BRCA1/2 carriers.

Lynch syndrome: the influence of environmental factors on extracolonic cancer risk in hMLH1 c.C1528T mutation carriers and their mutation-negative sisters.

A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype.

Prevalence of BRCA2 and CDKN2a mutations in German familial pancreatic cancer families.

Identification of the first case of germline duplication of BRCA1 exon 13 in an Italian family.

LOH analysis should not be used as a tool to assess whether UVs of BRCA1/2 are pathogenic or not.

A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma.

Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma.

Successful oxytocin-assisted nipple aspiration in women at increased risk for breast cancer.

Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis.

Erratum to: Survey of familial glioma and role of germline p16<sup> INK4A</sup>/ p14<sup> ARF</sup> and p53 mutation.

Survey of familial glioma and role of germline p16<sup> INK4A</sup> /p14<sup> ARF</sup> and p53 mutation.

Screening for germline DND1 mutations in testicular cancer patients.

Familial adenomatous polyposis (FAP) and gender. Does gender influence the genetic transmission of FAP?

Surgical prophylaxis in familial adenomatous polyposis: do pre-existing desmoids outside the abdominal cavity matter?

Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes.