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Familial Cancer

Articles from the last few issues of Familial Cancer © Springer
  • Patient preferences regarding recontact by cancer genetics clinicians
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 265-273.
  • Recurrent idiopathic pancreatitis in familial adenomatous polyposis: Report of a case-series and review of the literature
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 275-280.
  • Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 281-286.
  • Adult weight gain and central obesity in women with and without a family history of breast cancer: a case control study
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 287-294.
  • Hysteroscopic findings in women at risk of HNPCC. Results of a prospective observational study
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 295-299.
  • Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 301-310.
  • Two TP53 germline mutations in a classical Li-Fraumeni syndrome family
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 311-316.
  • An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 317-321.
  • Disseminating risk information to familial adenomatous polyposis families
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 323-324.
  • The 2nd Biennial Scientific Meeting of International Society for Gastrointestinal Hereditary Tumours: The 2nd InSiGHT, Tuesday March 27Friday March 30, 2007, 5th Floor, Conference Center, Pacifico-Yokohama, Japan
    Familial Cancer, Vol. 6, No. 3. (September 2007), pp. 325-407.
  • Foreword
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 161-162.
  • Delivering cancer genetics services-new ways of working
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 163-167.
  • Competences, education and support for new roles in cancer genetics services: outcomes from the cancer genetics pilot projects
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 171-180.
  • The Teesside Cancer Family History Service: change management and innovation at cancer network level
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 181-187.
  • Providing a community-based cancer risk assessment service for a socially and ethnically diverse population
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 189-195.
  • Improving access to cancer genetics services in primary care: socio-economic data from North Kirklees
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 197-203.
    by Srinivasa, , Rowett, , Dharni, , Bhatt, , Day, , Chu,
  • Nurse-led cancer genetics clinics in primary and secondary care in varied ethnic population areas: interaction with primary care to improve ascertainment of individuals from ethnic minorities
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 205-212.
  • Delivery of cancer genetics services: The Royal Marsden telephone clinic model
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 213-219.
  • Cancer genetics in rural primary care: a pilot nurse-led service using a new mobile IT system
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 221-229.
  • Patient perspectives on the Poole PCT cancer genetics service
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 231-239.
  • The role of patient users in cancer genetics services in primary care
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 241-248.
  • Sharing experiences of user involvement in shaping new services: the story of a national patient group
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 249-256.
  • National evaluation of NHS genetics service investments: emerging issues from the cancer genetics pilots
    Familial Cancer, Vol. 6, No. 2. (June 2007), pp. 257-263.
  • The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 1-12.
  • The management of families affected by hereditary non-polyposis colorectal cancer (HNPCC)
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 13-19.
  • Molecular diagnosis of neurofibromatosis type 1: 2 years experience
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 21-34.
  • Occurrence of both breast and ovarian cancer in a woman is a marker for the BRCA gene mutations: a population-based study from Western Sweden
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 35-41.
  • The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 43-51.
  • Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 53-62.
  • Risks of cancer due to a single BRCA1 mutation in an extended Utah kindred
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 63-71.
  • Identification of a founder BRCA2 mutation in Sardinian breast cancer families
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 73-79.
  • Familial colorectal cancer referral to regional genetics departmenta single centre experience
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 81-87.
  • An association between the 4G polymorphism in the PAI-1 promoter and the development of aggressive fibromatosis (desmoid tumor) in familial adenomatous polyposis patients
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 89-95.
  • A missense germline mutation in exon 7 of the MSH2 gene in a HNPCC family from center-Italy
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 97-102.
  • Study comparing two types of screening provision for people with von Hippel-Lindau disease
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 103-111.
  • Improved survival in BRCA2 carriers with ovarian cancer
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 113-119.
  • The interval between cancer diagnosis among mothers and offspring in a population-based cohort
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 121-129.
  • Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 131-134.
  • Utility of computed tomographic colonography in surveillance for hereditary nonpolyposis colorectal cancer syndrome.
    Fam Cancer (2 February 2007)
    by Laura Renkonen-Sinisalo, Arto Kivisaari, Leena Kivisaari, Seppo Sarna, Heikki J Järvinen
    posted by 1 person Terkko
  • A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 141-145.
  • Gastric carcinoid: germline and somatic mutation of the neurofibromatosis type 1 gene
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 147-152.
  • Heterozygote BRCA1 status and skewed chromosome X inactivation
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 153-157.
  • Acceptance of preventive surgeries by Israeli women who had undergone BRCA testing
    Familial Cancer, Vol. 6, No. 1. (March 2007), pp. 159-159.
  • Analysis of referrals to a multi-disciplinary breast cancer genetics clinic: practical and economic considerations
    Familial Cancer, Vol. 5, No. 4. (November 2006), pp. 297-303.
  • Low Frequency of CHEK2 Mutations in Familial Pancreatic Cancer
    Familial Cancer, Vol. 5, No. 4. (November 2006), pp. 305-308.
  • Family History, and Impact on Clinical Presentation and Prognosis, in a Population-based Breast Cancer Cohort from the Stockholm County
    Familial Cancer, Vol. 5, No. 4. (November 2006), pp. 309-321.
  • Low Prevalence of BRCA1 Exon Rearrangements in Familial and Young Sporadic Breast Cancer Patients
    Familial Cancer, Vol. 5, No. 4. (November 2006), pp. 323-326.
  • Acceptance of Preventive Surgeries by Israeli Women Who had Undergone BRCA Testing
    Familial Cancer, Vol. 5, No. 4. (November 2006), pp. 327-335.
  • Accuracy of BRCA1 and BRCA2 Founder Mutation Analysis in Formalin-Fixed and Paraffin-Embedded (FFPE) Tissue
    Familial Cancer, Vol. 5, No. 4. (November 2006), pp. 337-342.
  • Differences of Onset Age and Survival Rates in Esophageal Squamous Cell Carcinoma Cases with and without Family History of Upper Gastrointestinal Cancer from a High-incidence Area in North China
    Familial Cancer, Vol. 5, No. 4. (November 2006), pp. 343-352.
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