Volume 11, Issue 2

Search all Familial Cancer articles

June 2012

18 articles in this issue

Hereditary medullary thyroid carcinoma: the management dilemma
Ping Zhou
Jian Liu
Ling Peng
Review 20 December 2011 Pages: 157 - 165
Management of duodenal adenomatosis in FAP: single centre experience
Musa Drini
Anthony Speer
Finlay A. Macrae
Original Article 01 December 2011 Pages: 167 - 173
Preimplantation genetic diagnosis for inherited breast cancer: first clinical application and live birth in Spain
Teresa Ramón y Cajal
Ana Polo
Joaquin Calaf
Original Article 18 December 2011 Pages: 175 - 179
Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German families
S. M. Schneegans
A. Rosenberger
M. Shoukier
Original Article Open access 13 December 2011 Pages: 181 - 188
A novel germline SDHB mutation in a gastrointestinal stromal tumor patient without bona fide features of the Carney–Stratakis dyad
Ricardo Celestino
Jorge Lima
José Manuel Lopes
Original Article 10 December 2011 Pages: 189 - 194
Urologists’ and GPs’ knowledge of hereditary prostate cancer is suboptimal for prostate cancer counseling: a nation-wide survey in The Netherlands
Ruben Cremers
Christi van Asperen
Lambertus Kiemeney
Original Article Open access 11 December 2011 Pages: 195 - 200
Analysis of the miR-34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening
Angela M. Cozzolino
Lucia Pedace
Paola Grammatico
Original Article 25 December 2011 Pages: 201 - 208
Active surveillance of renal masses in von Hippel-Lindau disease: growth rates and clinical outcome over a median follow-up period of 56 months
Jin Zhang
Jia-Hua Pan
Yi-Ran Huang
Original Article 28 December 2011 Pages: 209 - 214
Looking different, feeling different: women’s reactions to risk-reducing breast and ovarian surgery
Nina Hallowell
Brandi Baylock
Melanie A. Price
Original Article 24 December 2011 Pages: 215 - 224
RB1 mutations and second primary malignancies after hereditary retinoblastoma
Charlotte J. Dommering
Tamara Marees
Annette C. Moll
Original Article Open access 29 December 2011 Pages: 225 - 233
Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations
A. Moran
C. O’Hara
D. G. R. Evans
Original Article 21 December 2011 Pages: 235 - 242
The founder Ashkenazi Jewish mutations in the MSH2 and MSH6 genes in Israeli patients with gastric and pancreatic cancer
Yael Laitman
Liron Herskovitz
Eitan Friedman
Original Article 04 January 2012 Pages: 243 - 247
Can a gastrointestinal pathologist identify microsatellite instability in colorectal cancer with reproducibility and a high degree of specificity?
Eli Brazowski
Paul Rozen
Guy Rosner
Original Article 13 January 2012 Pages: 249 - 257
Psychological distress in newly diagnosed colorectal cancer patients following microsatellite instability testing for Lynch syndrome on the pathologist’s initiative
K. M. Landsbergen
J. B. Prins
N. Hoogerbrugge
Original Article Open access 07 February 2012 Pages: 259 - 267
French women’s breast self-examination practices with time after undergoing BRCA1/2 genetic testing
C. Maheu
T. Apostolidis
C. Julian-Reynier
Original Article 18 February 2012 Pages: 269 - 278
Predictive genetic testing of first degree relatives of mutation carriers is a cost-effective strategy in preventing hereditary non-polyposis colorectal cancer in Singapore
Vivian Wei Wang
Poh Koon Koh
Jeremy Fung Yen Lim
Original Article 17 February 2012 Pages: 279 - 289
Families’ experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population
Álvaro Mendes
Liliana Sousa
Original Article 25 February 2012 Pages: 291 - 306
Prevalence of TP53 germ line mutations in young Pakistani breast cancer patients
Muhammad U. Rashid
Sidra Gull
Ute Hamann
Short Communication 07 February 2012 Pages: 307 - 311

Volume 11, Issue 2

Hereditary medullary thyroid carcinoma: the management dilemma

Management of duodenal adenomatosis in FAP: single centre experience

Preimplantation genetic diagnosis for inherited breast cancer: first clinical application and live birth in Spain

Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German families

A novel germline SDHB mutation in a gastrointestinal stromal tumor patient without bona fide features of the Carney–Stratakis dyad

Urologists’ and GPs’ knowledge of hereditary prostate cancer is suboptimal for prostate cancer counseling: a nation-wide survey in The Netherlands

Analysis of the miR-34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening

Active surveillance of renal masses in von Hippel-Lindau disease: growth rates and clinical outcome over a median follow-up period of 56 months

Looking different, feeling different: women’s reactions to risk-reducing breast and ovarian surgery

RB1 mutations and second primary malignancies after hereditary retinoblastoma

Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations

The founder Ashkenazi Jewish mutations in the MSH2 and MSH6 genes in Israeli patients with gastric and pancreatic cancer

Can a gastrointestinal pathologist identify microsatellite instability in colorectal cancer with reproducibility and a high degree of specificity?

Psychological distress in newly diagnosed colorectal cancer patients following microsatellite instability testing for Lynch syndrome on the pathologist’s initiative

French women’s breast self-examination practices with time after undergoing BRCA1/2 genetic testing

Predictive genetic testing of first degree relatives of mutation carriers is a cost-effective strategy in preventing hereditary non-polyposis colorectal cancer in Singapore

Families’ experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population

Prevalence of TP53 germ line mutations in young Pakistani breast cancer patients

Navigation