Volume 12, Issue 3

Search all Familial Cancer articles

September 2013

Special Issue: Birt–Hogg–Dubé syndrome.

Issue Editors:

Maria F Czyzyk-Krzeska,
Francis X McCormack

31 articles in this issue

Birt–Hogg–Dubé syndrome
Maria F. Czyzyk-Krzeska
Francis X. McCormack
Forward 27 September 2013 Pages: 355 - 356
Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
Laura S. Schmidt
OriginalPaper 30 October 2012 Pages: 357 - 364
Erratum to: Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
Laura S. Schmidt
Erratum 08 January 2013 Pages: 365 - 365
Birt–Hogg–Dubé: tumour suppressor function and signalling dynamics central to folliculin
Andrew R. Tee
Arnim Pause
Original Article 25 October 2012 Pages: 367 - 372
A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation
Fred H. Menko
Paul C. Johannesma
Johan J. P. Gille
Original Article 22 December 2012 Pages: 373 - 379
Birt–Hogg–Dubé syndrome and the skin
Marigje Vernooij
Tijs Claessens
Barry J. Coull
Original Article 10 January 2013 Pages: 381 - 385
Pulmonary manifestations of Birt-Hogg-Dubé syndrome
Nishant Gupta
Kuniaki Seyama
Francis X. McCormack
Original Article 29 May 2013 Pages: 387 - 396
Diagnosis and management of BHD-associated kidney cancer
Lambros Stamatakis
Adam R. Metwalli
W. Marston Linehan
Original Article 24 May 2013 Pages: 397 - 402
Erratum to: Birt–Hogg–Dubé: beyond the clinical manifestations
Lindsay A. Middelton
Erratum 31 July 2013 Pages: 403 - 403
Abstracts

Abstracts 24 September 2013 Pages: 405 - 448
The prognostic value of MGMT promoter methylation in Glioblastoma multiforme: a meta-analysis
Kui Zhang
Xiao-qin Wang
Lin Zhang
Review 09 February 2013 Pages: 449 - 458
Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis
Driss Ait Ouakrim
Trevor Lockett
Mark A. Jenkins
Review Article 23 May 2013 Pages: 459 - 472
The risk of gastric cancer in carriers of CHEK2 mutations
Urszula Teodorczyk
Cezary Cybulski
Jan Lubiński
Original Article 08 January 2013 Pages: 473 - 478
Body image issues after bilateral prophylactic mastectomy with breast reconstruction in healthy women at risk for hereditary breast cancer
Jessica P. Gopie
Marc A. M. Mureau
Aad Tibben
Original Article 08 December 2012 Pages: 479 - 487
Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern India
Abhijit Chakraborty
Ashis Mukhopadhyay
Jayasri Basak
Original Article 12 December 2012 Pages: 489 - 495
Cancer family history triage: a key step in the decision to offer screening and genetic testing
Paul Brennan
Oonagh Claber
Tracey Brennan
Original Article 14 December 2012 Pages: 497 - 502
Searching for E-cadherin gene mutations in early onset diffuse gastric cancer and hereditary diffuse gastric cancer in Korean patients
Sollip Kim
Jun-Won Chung
Jin-Ho Kim
Original Article 21 December 2012 Pages: 503 - 507
Unmet support needs and distress among women with a BRCA1/2 mutation
Ashley Farrelly
Victoria White
Jessica Duffy
Original Article 23 December 2012 Pages: 509 - 518
Detection of large deletions in the VHL gene using a Real-Time PCR with SYBR Green
Andrew Ebenazer
Simon Rajaratnam
Rekha Pai
Original Article 09 February 2013 Pages: 519 - 524
Familial adenomatous polyposis: not all masses are desmoids
J. Sloane
P. Ranchod
S. K. Clark
Original Article 10 February 2013 Pages: 525 - 528
Mutation screening in a Norwegian cohort with pheochromocytoma
Wenche Sjursen
Henrik Halvorsen
Jan E. Varhaug
Original Article 14 February 2013 Pages: 529 - 535
Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial
Susan V. Montgomery
Andrea M. Barsevick
Mary B. Daly
Original Article 19 February 2013 Pages: 537 - 546
Mutation screen and RNA analysis disclose the changed splicing of the E-cadherin transcription in gastric cancer
Xiaowei Li
Yafan Gao
Yaping Wang
Original Article 23 February 2013 Pages: 547 - 554
Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes
Marcia Cruz-Correa
Yaritza Diaz-Algorri
Segundo Rodriguez-Quilichini
Original Article 05 March 2013 Pages: 555 - 562
Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?
Mark Clendenning
Michael D. Walsh
Daniel D. Buchanan
Short Communication 04 January 2013 Pages: 563 - 566
Splice site mutations in mismatch repair genes and risk of cancer in the general population
Mette Thomsen
Børge G. Nordestgaard
Stig E. Bojesen
Short Communication 18 January 2013 Pages: 567 - 572
A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis
Maurizio Ponz de Leon
Claudia Bertarelli
Elio Jovine
Short Communication 30 November 2012 Pages: 573 - 576
A complex endocrine conundrum
G. Bano
V. Siedel
S. Hodgson
Short Communication 15 December 2012 Pages: 577 - 580
GNAS is not involved in gastrointestinal tumour formation in Peutz-Jeghers syndrome
Susanne E. Korsse
Maikel P. Peppelenbosch
Wendy van Veelen
Letter to the Editor 22 January 2013 Pages: 581 - 582
Erratum to: Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis
Kory W. Jasperson
Thuy M. Vu
Jeffrey N. Weitzel
Erratum 06 February 2013 Pages: 583 - 583
Erratum to: Closing the loop: an interactive action research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial needs post-genetic cancer risk assessment
Deborah J. MacDonald
Julia Deri
Kathleen R. Blazer
Erratum 06 February 2013 Pages: 585 - 585

Volume 12, Issue 3

Birt–Hogg–Dubé syndrome

Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies

Erratum to: Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies

Birt–Hogg–Dubé: tumour suppressor function and signalling dynamics central to folliculin

A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation

Birt–Hogg–Dubé syndrome and the skin

Pulmonary manifestations of Birt-Hogg-Dubé syndrome

Diagnosis and management of BHD-associated kidney cancer

Erratum to: Birt–Hogg–Dubé: beyond the clinical manifestations

Abstracts

The prognostic value of MGMT promoter methylation in Glioblastoma multiforme: a meta-analysis

Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis

The risk of gastric cancer in carriers of CHEK2 mutations

Body image issues after bilateral prophylactic mastectomy with breast reconstruction in healthy women at risk for hereditary breast cancer

Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern India

Cancer family history triage: a key step in the decision to offer screening and genetic testing

Searching for E-cadherin gene mutations in early onset diffuse gastric cancer and hereditary diffuse gastric cancer in Korean patients

Unmet support needs and distress among women with a BRCA1/2 mutation

Detection of large deletions in the VHL gene using a Real-Time PCR with SYBR Green

Familial adenomatous polyposis: not all masses are desmoids

Mutation screening in a Norwegian cohort with pheochromocytoma

Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial

Mutation screen and RNA analysis disclose the changed splicing of the E-cadherin transcription in gastric cancer

Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes

Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?

Splice site mutations in mismatch repair genes and risk of cancer in the general population

A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis

A complex endocrine conundrum

GNAS is not involved in gastrointestinal tumour formation in Peutz-Jeghers syndrome

Erratum to: Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis

Erratum to: Closing the loop: an interactive action research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial needs post-genetic cancer risk assessment

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