Works matching IS 13899600 AND DT 2005 AND VI 4

Results: 69

Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 295, doi. 10.1007/s10689-005-0658-9

By:

Anja Wagner;
Ingrid van Kessel;
Mieke Kriege;
Carli Tops;
Juul Wijnen;
Hans Vasen;
Conny van der Meer;
Iris van Oostrom;
Hanne Meijers-Heijboer

Publication type:

Article

MLH1 and MSH2 Mutations in Colombian Families with Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome) – Description of Four Novel Mutations.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 285, doi. 10.1007/s10689-005-4523-7

By:

Alejandro Giraldo;
Andrea Gómez;
Gustavo Salguero;
Herbert García;
Fabio Aristizábal;
Óscar Gutiérrez;
Luis Ángel;
Jorge Padrón;
Carlos Martínez;
Humberto Martínez;
Omar Malaver;
Luis Flórez;
Rosa Barvo

Publication type:

Article

BAP1 and Breast Cancer Risk.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 273, doi. 10.1007/s10689-005-2833-4

By:

Isabelle Coupier;
Pierre-Yves Cousin;
David Hughes;
Patricia Legoix-Né;
Alexandra Trehin;
Olga Sinilnikova;
Dominique Stoppa-Lyonnet

Publication type:

Article

Linkage of a Pedigree Drawing Program and Database to a Program for Determining BRCA Mutation Carrier Probability.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 313, doi. 10.1007/s10689-005-8849-y

By:

Sharon Sand;
David DeRam;
Deborah MacDonald;
Kathleen Blazer;
Jeffrey Weitzel

Publication type:

Article

Key word Index Volume 4.

Published in:: Familial Cancer, 2005, v. 4, n. 4, p. 337, doi. 10.1007/s10689-005-4695-1
Publication type:: Article

Neurofibromatosis 2 (NF2) and Malignant Mesothelioma in a Man with a Constitutional NF2 Missense Mutation.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 321, doi. 10.1007/s10689-005-0659-8

By:

M.E. Baser;
H. Rai;
A.J. Wallace;
D.G.R. Evans

Publication type:

Article

Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like Families.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 291, doi. 10.1007/s10689-005-1255-7

By:

Shiri Dovrat;
Arie Figer;
Herma Fidder;
Pavlos Neophytou;
Zvi Fireman;
Ravit Geva;
Jamal Zidan;
Dov Flex;
Shimon Meir;
Eitan Friedman

Publication type:

Article

Survival of Patients with Ovarian Cancer due to a Mismatch Repair Defect.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 301, doi. 10.1007/s10689-005-6573-2

By:

Th.E.M. Crijnen;
M.L.G. Janssen-Heijnen;
H. Gelderblom;
J. Morreau;
M.A. Nooij;
G.G. Kenter;
H.F.A. Vasen

Publication type:

Article

Patient Satisfaction of BRCA1/2 Genetic Testing by Women at High Risk for Breast Cancer Participating in a Prevention Trial.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 279, doi. 10.1007/s10689-005-1474-y

By:

Jennifer R. Klemp;
Anne O’Dea;
Carolyn Chamberlain;
Carol J. Fabian

Publication type:

Article

Contents Volume 4.

Published in:: Familial Cancer, 2005, v. 4, n. 4, p. 339, doi. 10.1007/s10689-005-4696-0
Publication type:: Article

Acknowledgements.

Published in:: Familial Cancer, 2005, v. 4, n. 4, p. 335, doi. 10.1007/s10689-005-4694-2
Publication type:: Article

Behavioral and Economic Impact of a Familial History of Cancers.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 307, doi. 10.1007/s10689-005-3143-6

By:

Francois Eisinger;
Carole Tarpin;
Laetitia Huiart;
Doug Horsman;
Laetitia Rabayrol;
Remi Didelot;
Claire Julian-Reynier;
Hagay Sobol

Publication type:

Article

Syndrome of Early Onset Colon Cancers, Hematologic Malignancies & Features of Neurofibromatosis in HNPCC Families with Homozygous Mismatch Repair Gene Mutations.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 323, doi. 10.1007/s10689-005-8351-6

By:

Prathap Bandipalliam

Publication type:

Article

Lack of Germ-line Mutations at the Specific BRCA1-IRIS Coding Sequence in 114 Spanish High-risk Breast/ovarian Families.

Published in:

Familial Cancer, 2005, v. 4, n. 4, p. 317, doi. 10.1007/s10689-005-1236-x

By:

Miguel de la Hoya;
Juan Fernández;
Ana de Abajo;
Alicia Tosar;
Eduardo Díaz-Rubio;
Trinidad Caldés

Publication type:

Article

The Incidence of Lynch Syndrome.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 233

By:

Albert de la Chapelle

Publication type:

Article

Clinical Description of the Lynch Syndrome [Hereditary Nonpolyposis Colorectal Cancer (HNPCC)].

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 219, doi. 10.1007/s10689-004-3906-5

By:

H. F. A. Vasen

Publication type:

Article

Gynecologic Cancers in Lynch Syndrome/HNPCC.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 249, doi. 10.1007/s10689-005-1838-3

By:

H. Karen Lu;
Russell R. Broaddus

Publication type:

Article

Lynch Syndrome Genes.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 227

By:

Päivi Peltomäki

Publication type:

Article

Use of Microsatellite Instability and Immunohistochemistry Testing for the Identification of Individuals at Risk for Lynch Syndrome.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 255, doi. 10.1007/s10689-004-1447-6

By:

Linnea M. Baudhuin;
Lawrence J. Burgart;
Olga Leontovich;
Stephen N. Thibodeau

Publication type:

Article

Surveillance in Lynch Syndrome.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 267, doi. 10.1007/s10689-005-1475-x

By:

Jukka-Pekka Mecklin;
Heikki J. Järvinen

Publication type:

Article

Introduction.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 209, doi. 10.1007/s10689-004-2526-4

By:

Henry T. Lynch

Publication type:

Article

Evolution of the Nomenclature for the Hereditary Colorectal Cancer Syndromes.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 211, doi. 10.1007/s10689-004-4489-x

By:

C. Richard Boland

Publication type:

Article

The Tumor Spectrum in the Lynch Syndrome.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 245, doi. 10.1007/s10689-004-7994-z

By:

Patrice Watson;
Bronson Riley

Publication type:

Article

Guest editorial.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 207, doi. 10.1007/s10689-005-8658-3

By:

C. Richard Boland

Publication type:

Article

Frequency of Familial Colon Cancer and Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) in a Large Population Database.

Published in:

Familial Cancer, 2005, v. 4, n. 3, p. 239, doi. 10.1007/s10689-005-0657-x

By:

Richard A. Kerber;
Deborah W. Neklason;
Wade S. Samowitz;
Randall W. Burt

Publication type:

Article

Informing one’s family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory study.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 163, doi. 10.1007/s10689-004-7992-1

By:

Ilse Mesters;
Marlein Ausems;
Sophie Eichhorn;
Hans Vasen

Publication type:

Article

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 syndrome.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 139, doi. 10.1007/s10689-004-2759-2

By:

H. R. Murphy;
W. Taylor;
A. Ellis;
R. Sturgess

Publication type:

Article

Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 115, doi. 10.1007/s10689-004-7991-2

By:

Karin Landsbergen;
Chris Verhaak;
Floor Kraaimaat;
Nicoline Hoogerbrugge

Publication type:

Article

A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 127, doi. 10.1007/s10689-004-5814-0

By:

Brindusa Truta;
Brian A. Allen;
Peggy G. Conrad;
Vivian Weinberg;
Glenn A. Miller;
Rob Pomponio;
Lara R. Lipton;
Germano Guerra;
Ian P. M. Tomlinson;
Marvin H. Sleisenger;
Young S. Kim;
Jonathan P. Terdiman

Publication type:

Article

The BRCA1 exon 13 duplication in the Swedish population.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 191, doi. 10.1007/s10689-004-7023-2

By:

Barbara Kremeyer;
Maria Soller;
Kristina Lagerstedt;
Paula Maguire;
Sylvie Mazoyer;
Margareta Nordling;
Jan Wahlström;
Annika Lindblom

Publication type:

Article

The CHEK2 1100delC allele is not relevant for risk assessment in HNPCC and HBCC Spanish families.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 183

By:

Ana Sánchez de Abajo;
Miguel de la Hoya;
Javier Godino;
Vicente Furió;
Alicia Tosar;
Pedro Pérez-Segura;
Eduardo Díaz-Rubio;
Trinidad Caldés

Publication type:

Article

APC and β-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 187, doi. 10.1007/s10689-004-6130-4

By:

Reetta Kariola;
Wael M. Abdel-Rahman;
Miina Ollikainen;
Ralf Butzow;
Päivi Peltomäki;
Minna Nyström

Publication type:

Article

Referrals of patients to colorectal cancer genetics services in south-east Scotland.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 151, doi. 10.1007/s10689-004-4488-y

By:

Susan Holloway;
Mary Porteous;
Roseanne Cetnarskyj;
Robert Rush;
Sally Appleton;
Dermot Gorman;
Harry Campbell

Publication type:

Article

Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 145, doi. 10.1007/s10689-004-6131-3

By:

Seyed Mohammad Akrami;
Malcolm G. Dunlop;
Susan M. Farrington;
Ian M. Frayling;
Fiona MacDonald;
John F. Harvey;
John A. L. Armour

Publication type:

Article

The use of preventive measures among healthy women who carry a BRCA1 or BRCA2 mutation.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 97, doi. 10.1007/s10689-005-4215-3

By:

Kelly A. Metcalfe;
Carrie Snyder;
Jennifer Seidel;
Danielle Hanna;
Henry T. Lynch;
Steven Narod

Publication type:

Article

Measurement of psychological factors associated with genetic testing for hereditary breast, ovarian and colon cancers.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 195, doi. 10.1007/s10689-004-1446-7

By:

Susan T. Vadaparampil;
Mary Ropka;
Michael E. Stefanek

Publication type:

Article

High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in Latvia.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 77, doi. 10.1007/s10689-004-2758-3

By:

Laima Tikhomirova;
Olga Sinicka;
Dagnija Smite;
Janis Eglitis;
Shirley V. Hodgson;
Aivars Stengrevics

Publication type:

Article

The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li–Fraumeni-like kindreds.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 177, doi. 10.1007/s10689-004-1946-5

By:

Rina Siddiqui;
Kenan Onel;
Flavia Facio;
Kedoudja Nafa;
Louis Robles Diaz;
Noah Kauff;
Helen Huang;
Mark Robson;
Nathan Ellis;
Kenneth Offit

Publication type:

Article

Abdominal desmoid in familial adenomatous polyposis presenting as a pancreatic cystic lesion.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 135, doi. 10.1007/s10689-004-1923-z

By:

Lana N. Pho;
Cheryl M. Coffin;
Randall W. Burt

Publication type:

Article

Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 73, doi. 10.1007/s10689-004-2102-y

By:

G. Chenevix-Trench;
O. M. Sinilnikova;
G. Suthers;
N. Pandeya;
S. Mazoyer;
J. F. Sambrook;
S. Goldup;
D. Goldgar;
H. T. Lynch;
G. M. Lenoir;
G. Cheetham;
kConFab

Publication type:

Article

Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 121, doi. 10.1007/s10689-004-7995-y

By:

Amy Østertun Geirdal;
Jon G. Reichelt;
Alv A. Dahl;
Ketil Heimdal;
Lovise Mæhle;
Astrid Stormorken;
Pål Møller

Publication type:

Article

Predictors of participation in clinical and psychosocial follow-up of the kConFab breast cancer family cohort.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 105, doi. 10.1007/s10689-004-6129-x

By:

Kelly-Anne Phillips;
Phyllis N. Butow;
Ailsa E. Stewart;
Jiun-Horng Chang;
Prue C. Weideman;
Melanie A. Price;
Sue Anne McLachlan;
kConFab Investigators;
Geoffrey J. Lindeman;
Michael J. McKay;
Michael L. Friedlander;
John L. Hopper

Publication type:

Article

The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi Jews.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 85, doi. 10.1007/s10689-004-2101-z

By:

Lluís Quintana-Murci;
Inbar Gal;
Tangiz Bakhan;
Hélène Quach;
S Hamid Sayar;
Ronit Shiri-Sverdlov;
Ruth Gershoni Baruch;
Ken McElreavey;
Efrat Dagan;
Steven Narod;
Eitan Friedman

Publication type:

Article

SISE matters: the Sum of Information on Seventy-yr-old Equivalents measures pedigree information content when assessing the risk of HNPCC in a family.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 169, doi. 10.1007/s10689-004-7251-5

By:

R. C. Green;
J. R. McLaughlin;
H. B. Younghusband

Publication type:

Article

A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques.

Published in:

Familial Cancer, 2005, v. 4, n. 2, p. 89, doi. 10.1007/s10689-004-5812-2

By:

Annika Bergman;
Anna Flodin;
Yvonne Engwall;
Eva L. Arkblad;
Kerstin Berg;
Zakaria Einbeigi;
Tommy Martinsson;
Jan Wahlström;
Per Karlsson;
Margareta Nordling

Publication type:

Article

Abstracts of the 1st Conference of InSiGHT, the International Society for Gastrointestinal Hereditary Tumors, Newcastle upon Tyne, United Kingdom, 14-17 June 2005.

Published in:: Familial Cancer, 2005, v. 4, p. 25, doi. 10.1007/s10689-005-4150-3
Publication type:: Article

Poster Presentations.

Published in:: Familial Cancer, 2005, v. 4, p. 63
Publication type:: Article

Free Paper Session 7.

Published in:: Familial Cancer, 2005, v. 4, p. 57
Publication type:: Article

Free Paper Session 6.

Published in:: Familial Cancer, 2005, v. 4, p. 55
Publication type:: Article

Free Paper Session 5.

Published in:: Familial Cancer, 2005, v. 4, p. 52
Publication type:: Article