نتایج جستجو برای: hereditary breast cancer

تعداد نتایج: 1055993  

1999
J. Gronwald J. Menkiszak T. Huzarski T. Byrski A. Jakubowska S. Zajàczek A. Toloczko J. Podolski B. Górecka H. Zdziebkowska P. Stanislawski M. Stawicka J. Lubinski

Cancer Genetic Centres in Poland have been established in Bydgoszcz, Gdansk, Gliwice, Kraków, Poznan, Szczecin and Wroclaw. They provide genetic counselling and surveillance for high-risk families. Training courses for postgraduates organized under the supervision of the Hereditary Cancer Centre (HCC) in Szczecin include: a) a yearly 3day training programme for genetic professionals, b) a yearl...

Journal: :Siberian journal of oncology 2019

Journal: :Journal of the National Cancer Institute. Monographs 2008
Noralane M Lindor Mary L McMaster Carl J Lindor Mark H Greene

1. Ataxia Telangiectasia (includes Ataxia Telangiectasia 12 Complementation Groups A, C, D, E, Louis–Barr Syndrome) 2. Basal Cell Nevus Syndrome, Nevoid Basal Cell 18 Carcinoma Syndrome, or Gorlin Syndrome 3. Beckwith–Wiedemann Syndrome 19 (Exomphalos–Macroglossia–Gigantism Syndrome) 4. Birt–Hogg–Dubé Syndrome 20 5. Bloom Syndrome 21 6. Breast/Ovarian Cancer, Hereditary (BRCA1) 22 7. Breast/Ova...

Journal: :The Ulster Medical Journal 1996
A. G. McKinley S. E. Russell R. A. Spence W. Odling-Smee N. C. Nevin

The aim of this investigation was to document hereditary breast cancer in Northern Ireland. Family history details from over nine hundred women were obtained by postal survey and one hundred and twenty nine home visits were carried out to collect pedigree information. The families documented varied in the number of affected women from three, which was the minimum criteria for inclusion, to a ma...

2017
Iván Márquez-Rodas Marina Pollán María José Escudero Amparo Ruiz Miguel Martín Ana Santaballa Purificación Martínez del Prado Norberto Batista Raquel Andrés Antonio Antón Antonio Llombart Antonio Fernandez Aramburu Encarnación Adrover Sonia González Miguel Angel Seguí Lourdes Calvo José Lizón Álvaro Rodríguez Lescure Teresa Ramón y Cajal Gemma Llort Carlos Jara Eva Carrasco Sara López-Tarruella

PURPOSE To determine the frequency of breast cancer (BC) patients with hereditary risk features in a wide retrospective cohort of patients in Spain. METHODS a retrospective analysis was conducted from 10,638 BC patients diagnosed between 1998 and 2001 in the GEICAM registry "El Álamo III", dividing them into four groups according to modified ESMO and SEOM hereditary cancer risk criteria: Spor...

2014
Nahid Karimian Fathi Mahmood Shekari Khaniani Vahid Montazeri Sima Mansoori Derakhshan

OBJECTIVE(S) Breast cancer is the most common cancer in women. Every year, one million new cases are reported worldwide, representing 18% of the total number of cancer in women. Hereditary BRCA1 and BRCA2 mutations account for about 60% of inherited breast cancer and are the only known causes of hereditary breast cancer syndrome. The aim of this study was to determine the frequency of BRCA2 (ex...

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