Items where Author is "Erlic, Zoran"

2011

Frank-Raue, Karin and Rybicki, Lisa A. and Erlic, Zoran and Schweizer, Heiko and Winter, Aurelia and Milos, Ioana and Toledo, Sergio P. A. and Toledo Rodrigo, A. and Tavares Marcos, R. and Alevizaki, Maria and Mian, Caterina and Siggelkow, Heide and Hüfner, Michael and Wohllk, Nelson and Opocher, Giuseppe and Dvo áková, Sárka and Bendlova, Bela and Czetwertynska, Ma gorzata and Skasko, El bieta and Barontini, Marta and Sanso, Gabriela and Vorländer, Christian and Maia, Ana Luiza and Patocs, Attila and Links Thera, P. and de Groot, Jan Willem and Kerstens Michiel, N. and Valk Gerlof, D. and Miehle, Konstanze and Musholt, Thomas J. and Biarnes, Josefina and Damjanovic, Svetozar and Muresan, Mihaela and Wüster, Christian and Fassnacht, Martin and Peczkowska, Mariola and Fauth, Christine and Golcher, Henriette and Walter, Martin A. and Pichl, Josef and Raue, Friedhelm and Eng, Charis and Neumann, Hartmut P. H.. (2011) Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, Vol. 32, H. 1. pp. 51-58.

2010

Sullivan, Maren and Erlic, Zoran and Hoffmann, Michael M. and Arbeiter, Klaus and Patzer, Ludwig and Budde, Klemens and Hoppe, Bernd and Zeier, Martin and Lhotta, Karl and Rybicki, Lisa A. and Bock, Andreas and Berisha, Gani and Neumann, Hartmut P. H.. (2010) Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome. Annals of human genetics, Vol. 74, H. 1. pp. 17-26.

2009

Erlic, Zoran and Rybicki, Lisa and Peczkowska, Mariola and Golcher, Henriette and Kann, Peter H. and Brauckhoff, Michael and Müssig, Karsten and Muresan, Michaela and Schäffler, Andreas and Reisch, Nicole and Schott, Matthias and Fassnacht, Martin and Opocher, Giuseppe and Klose, Silke and Fottner, Christian and Forrer, Flavio and Plöckinger, Ursula and Petersenn, Stephan and Zabolotny, Dimitry and Kollukch, Oleg and Yaremchuk, Svetlana and Januszewicz, Andrzej and Walz, Martin K. and Eng, Charis and Neumann, Hartmut P. H. and European-American Pheochromocytoma Study Group, . (2009) Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients. Clinical cancer research : a journal of clinical and translational research, Vol. 15. pp. 6378-6385.