Ausgabe 2/2013
100 years of Lynch Syndrome
Inhalt (25 Artikel)
A hundred years of Lynch syndrome research (1913–2013)
Hans F. A. Vasen, Wouter H. de Vos tot Nederveen Cappel
The mechanism of mismatch repair and the functional analysis of mismatch repair defects in Lynch syndrome
Juana V. Martín-López, Richard Fishel
EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients
Marjolijn J. L. Ligtenberg, Roland P. Kuiper, Ad Geurts van Kessel, Nicoline Hoogerbrugge
The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome
J. P. Plazzer, R. H. Sijmons, M. O. Woods, P. Peltomäki, B. Thompson, J. T. Den Dunnen, F. Macrae
Gene variants of unknown clinical significance in Lynch syndrome. An introduction for clinicians
Rolf H. Sijmons, Marc S. Greenblatt, Maurizio Genuardi
Genetic modifiers of cancer risk in Lynch syndrome: a review
Bente A. Talseth-Palmer, Juul T. Wijnen, Desma M. Grice, Rodney J. Scott
Lynch syndrome-associated neoplasms: a discussion on histopathology and immunohistochemistry
Jinru Shia, Susanne Holck, Giovanni DePetris, Joel K. Greenson, David S. Klimstra
Colorectal surveillance in Lynch syndrome families
Wouter H. de Vos tot Nederveen Cappel, Heikki J. Järvinen, Patrick M. Lynch, Christoph Engel, Jukka-Pekka Mecklin, Hans F. A. Vasen
Role of new endoscopic techniques in Lynch syndrome
Jasmijn F. Haanstra, Jan H. Kleibeuker, Jan J. Koornstra
Endometrial and ovarian cancer in women with Lynch syndrome: update in screening and prevention
Karen H. Lu, Molly Daniels
Surveillance for urinary tract cancer in Lynch syndrome
Inge Thomsen Bernstein, Torben Myrhøj
Do lifestyle factors influence colorectal cancer risk in Lynch syndrome?
Fränzel J. B. van Duijnhoven, Akke Botma, Renate Winkels, Fokko M. Nagengast, Hans F. A. Vasen, Ellen Kampman
Surgical treatment of hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome)
Miguel A. Rodriguez-Bigas, Gabriela Möeslein
Towards a vaccine to prevent cancer in Lynch syndrome patients
Magnus von Knebel Doeberitz, Matthias Kloor
How do we approach the goal of identifying everybody with Lynch Syndrome?
Heather Hampel, Albert de la Chapelle
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists
Fred H. Menko, Cora M. Aalfs, Lidewij Henneman, Yrrah Stol, Miranda Wijdenes, Ellen Otten, Marleen M. J. Ploegmakers, Johan Legemaate, Ellen M. A. Smets, Guido M. W. R. de Wert, Aad Tibben
100 years lynch syndrome: what have we learned about psychosocial issues?
Eveline M. A. Bleiker, Mary Jane Esplen, Bettina Meiser, Helle Vendel Petersen, Andrea Farkas Patenaude
Value-based healthcare in Lynch syndrome
Simone D. Hennink, Nandy Hofland, Jessica P. Gopie, Corinne van der Kaa, Kimberley de Koning, Maartje Nielsen, Carli Tops, Hans Morreau, Wouter H. de Vos tot Nederveen Cappel, Alexandra M. J. Langers, James C. Hardwick, Katja N. Gaarenstroom, Rob A. Tollenaar, Roeland A. Veenendaal, Aad Tibben, Juul Wijnen, Magdalena van Heck, Christi van Asperen, Anne J. Roukema, Daan W. Hommes, Frederik J. Hes, Hans F. A. Vasen