Familial Cancer - 2005

61 articles | Last updated: 2025-12-03 14:12:56
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Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Syndrome of Early Onset Colon Cancers, Hematologic Malignancies & Features of Neurofibromatosis in HNPCC Families with Homozygous Mismatch Repair Gene Mutations
Neurofibromatosis 2 (NF2) and Malignant Mesothelioma in a Man with a Constitutional NF2 Missense Mutation
Patient Satisfaction of BRCA1/2 Genetic Testing by Women at High Risk for Breast Cancer Participating in a Prevention Trial
Key word Index Volume 4
Contents Volume 4
Linkage of a Pedigree Drawing Program and Database to a Program for Determining BRCA Mutation Carrier Probability
Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures
Lack of Germ-line Mutations at the Specific BRCA1-IRIS Coding Sequence in 114 Spanish High-risk Breast/ovarian Families
BAP1 and Breast Cancer Risk
Acknowledgements
Survival of Patients with Ovarian Cancer due to a Mismatch Repair Defect
Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like Families
Behavioral and Economic Impact of a Familial History of Cancers
MLH1 and MSH2 Mutations in Colombian Families with Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome) – Description of Four Novel Mutations
Introduction
Evolution of the Nomenclature for the Hereditary Colorectal Cancer Syndromes
Lynch Syndrome Genes
The Tumor Spectrum in the Lynch Syndrome
Frequency of Familial Colon Cancer and Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) in a Large Population Database
Use of Microsatellite Instability and Immunohistochemistry Testing for the Identification of Individuals at Risk for Lynch Syndrome
Clinical Description of the Lynch Syndrome [Hereditary Nonpolyposis Colorectal Cancer (HNPCC)]
The Incidence of Lynch Syndrome
Surveillance in Lynch Syndrome
Gynecologic Cancers in Lynch Syndrome/HNPCC
Guest editorial
Referrals of patients to colorectal cancer genetics services in south-east Scotland
SISE matters: the Sum of Information on Seventy-yr-old Equivalents measures pedigree information content when assessing the risk of HNPCC in a family
Abdominal desmoid in familial adenomatous polyposis presenting as a pancreatic cystic lesion
High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in Latvia
An unusual case of Turcot’s syndrome associated with ileal adenocarcinoma, intestinal non-Hodgkin’s lymphoma, and duodenal adenocarcinoma. Review of the classification and genetic basis of Turcot’s sy
The CHEK2 1100delC allele is not relevant for risk assessment in HNPCC and HBCC Spanish families
Predictors of participation in clinical and psychosocial follow-up of the kConFab breast cancer family cohort
Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH
Informing one’s family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory study
Measurement of psychological factors associated with genetic testing for hereditary breast, ovarian and colon cancers
The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li–Fraumeni-like kindreds
The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi Jews non-Jewish Iranians; French-Canadian; non-Ashkenazi Jews
Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers
A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques
A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history
APC and β-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers
The BRCA1 exon 13 duplication in the Swedish population
Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients
Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations
The use of preventive measures among healthy women who carry a BRCA1 or BRCA2 mutation
Pheochromocytoma – where are we? Where should we go? A medical and scientific odyssey
SDHC mutations in hereditary paraganglioma/pheochromocytoma
Paragangliomas of the head and neck: diagnosis and treatment
Imaging of pheochromocytoma and paraganglioma
Mutations of the SDHB and SDHD genes
Central nervous system manifestations in VHL: genetics, pathology and clinical phenotypic features
Multiple endocrine neoplasia type 2
Ophthalmological manifestations in VHL and NF 1: pathological and diagnostic implications
Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx
Pheochromocytoma in von Hippel–Lindau disease and neurofibromatosis type 1
Molecular pathogenesis of MEN2-associated tumors
Instructions for Authors
Origins of the Leeds Castle Polyposis Group
History of the International Collaborative Group on Hereditary NonPolyposis Colorectal Cancer
Author Index
Programme