Ausgabe 3/2009
Inhalt (14 Artikel)
Response to neo-adjuvant chemotherapy in BRCA1 and BRCA2 related stage III breast cancer
Ayala Hubert, Bela Mali, Tamar Hamburger, Yakir Rottenberg, Beatrice Uziely, Tamar Peretz, Luna Kadouri
A homozygote splice site PMS2 mutation as cause of Turcot syndrome gives rise to two different abnormal transcripts
Wenche Sjursen, Inga Bjørnevoll, Lars F. Engebretsen, Kristine Fjelland, Tore Halvorsen, Helge E. Myrvold
Homozygosity of MSH2 c.1906G→C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I
Helen Toledano, Yael Goldberg, Inbal Kedar-Barnes, Hagit Baris, Rinnat M. Porat, Chen Shochat, Dani Bercovich, Eli Pikarsky, Israela Lerer, Isaac Yaniv, Dvorah Abeliovich, Tamar Peretz
Consistency of self-reported first-degree family history of cancer in a population-based study
Fernanda Lenara Roth, Suzi Alves Camey, Maira Caleffi, Lavínia Schuler-Faccini, Edenir Inêz Palmero, Carla Bochi, Susana Mayer Moreira, Luciane Kalakun, Roberto Giugliani, Patrícia Ashton-Prolla
Haplotype and quantitative transcript analyses of Portuguese breast/ovarian cancer families with the BRCA1 R71G founder mutation of Galician origin
Catarina Santos, Ana Peixoto, Patrícia Rocha, Ana Vega, Maria José Soares, Nuno Cerveira, Susana Bizarro, Manuela Pinheiro, Deolinda Pereira, Helena Rodrigues, Fernando Castro, Rui Henrique, Manuel R. Teixeira
Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum
Mef Nilbert, Christina Therkildsen, Anja Nissen, Måns Åkerman, Inge Bernstein
Evidence of tumor microsatellite instability in gastric cancer with familial aggregation
Corrado Pedrazzani, Giovanni Corso, Sérgia Velho, Marina Leite, Valeria Pascale, Francesca Bettarini, Daniele Marrelli, Raquel Seruca, Franco Roviello
Men in the women’s world of hereditary breast and ovarian cancer—a systematic review
Nina Strømsvik, Målfrid Råheim, Nina Øyen, Eva Gjengedal
Lymphocyte recruitment into the tumor site is altered in patients with MSI-H colon cancer
Kristen M. Drescher, Poonam Sharma, Patrice Watson, Zoran Gatalica, Stephen N. Thibodeau, Henry T. Lynch
Health behaviors among Ashkenazi Jewish individuals receiving counseling for BRCA1 and BRCA2 mutations
Jackie Quach, Kyle Porter, Howard Leventhal, Kimberly M. Kelly
Breast cancer immunohistochemistry can be useful in triage of some HNPCC families
S. Shanley, C. Fung, J. Milliken, J. Leary, R. Barnetson, M. Schnitzler, J. Kirk
SDHB-associated renal oncocytoma suggests a broadening of the renal phenotype in hereditary paragangliomatosis
Alex Henderson, F. Douglas, P. Perros, C. Morgan, E. R. Maher
Familial nasopharyngeal carcinoma in Hong Kong: epidemiology and implication in screening
Wai Tong Ng, Cheuk Wai Choi, Michael C. H. Lee, Siu Hong Chan, Tsz Kok Yau, Anne W. M. Lee
Factors associated with intrusive cancer-related worries in women undergoing cancer genetic risk assessment
Paul Bennett, Clare Wilkinson, Jim Turner, Rhiannon Tudor Edwards, Barbara France, Gethin Griffith, Jonathon Gray