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Zoran Erlic

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Alexander Weber; Michael M Hoffmann; Hartmut P H Neumann; Zoran Erlic
Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytoma.
Francesca Schiavi; Elisa Taschin; Franco Trabalzini; Stefania Zovato; Theodoros Savvoukidis; Pietro Amistà; Mattia Barbareschi; Susi Barollo; Sara Bobisse; Fabio Branz; Maria Enrica Cecchini; Antonella Del Piano; Serena Demattè; Davide Donner; Zoran Erlic; Cesare Grandi; Franco Grego; Vittorio Manera; Fabio Marroni; Hartmut P H Neumann; Giuseppe Opocher
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression.
Nelson Wohllk; Heiko Schweizer; Zoran Erlic; Kurt Werner Schmid; Martin K Walz; Friedhelm Raue; Hartmut P H Neumann
Multiple endocrine neoplasia type 2.

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All Publications

2012: Alexander Weber; Michael M Hoffmann; Hartmut P H Neumann; Zoran Erlic
Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytoma.
Hormones & cancer 2012;3(4):187-92.
2012: Francesca Schiavi; Elisa Taschin; Franco Trabalzini; Stefania Zovato; Theodoros Savvoukidis; Pietro Amistà; Mattia Barbareschi; Susi Barollo; Sara Bobisse; Fabio Branz; Maria Enrica Cecchini; Antonella Del Piano; Serena Demattè; Davide Donner; Zoran Erlic; Cesare Grandi; Franco Grego; Vittorio Manera; Fabio Marroni; Hartmut P H Neumann; Giuseppe Opocher
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression.
The Journal of clinical endocrinology and metabolism 2012;97(4):E637-41.
2010: Nelson Wohllk; Heiko Schweizer; Zoran Erlic; Kurt Werner Schmid; Martin K Walz; Friedhelm Raue; Hartmut P H Neumann
Multiple endocrine neoplasia type 2.
Best practice & research. Clinical endocrinology & metabolism 2010;24(3):371-87.
2010: Maren Sullivan; Zoran Erlic; Michael M Hoffmann; Klaus Arbeiter; Ludwig Patzer; Klemens Budde; Bernd Hoppe; Martin Zeier; Karl Lhotta; Lisa A Rybicki; Andreas Bock; Gani Berisha; Hartmut P H Neumann
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome.
Annals of human genetics 2010;74(1):17-26.
2010: Zoran Erlic; Michael M Hoffmann; Maren Sullivan; Gerlind Franke; Mariola Peczkowska; Igor Harsch; Matthias Schott; Helmut E Gabbert; Matti Valimäki; Simon F Preuss; Kornelia Hasse-Lazar; Dariusz Waligorski; Mercedes Robledo; Andrzej Januszewicz; Charis Eng; Hartmut P H Neumann
Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.
The Journal of clinical endocrinology and metabolism 2010;95(1):308-13.
2009: José Gaal; Francien H van Nederveen; Zoran Erlic; Esther Korpershoek; Rogier Oldenburg; Carsten C Boedeker; Udo Kontny; Hartmut P H Neumann; Winand N M Dinjens; Ronald R de Krijger
Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome.
The Journal of clinical endocrinology and metabolism 2009;94(11):4367-71.
2009: Zoran Erlic; Lisa Rybicki; Mariola Peczkowska; Henriette Golcher; Peter H Kann; Michael Brauckhoff; Karsten Müssig; Michaela Muresan; Andreas Schäffler; Nicole Reisch; Matthias Schott; Martin Fassnacht; Giuseppe Opocher; Silke Klose; Christian Fottner; Flavio Forrer; Ursula Plöckinger; Stephan Petersenn; Dimitry Zabolotny; Oleg Kollukch; Svetlana Yaremchuk; Andrzej Januszewicz; Martin Walz; Charis Eng; Hartmut P H Neumann
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients.
Clinical cancer research : an official journal of the American Association for Cancer Research 2009;15(20):6378-85.
2009: Zoran Erlic; Hartmut P H Neumann
Diagnosing patients with hereditary paraganglial tumours.
The lancet oncology 2009;10(8):741.
2009: Carsten Christof Boedeker; Zoran Erlic; Stéphane Richard; Udo Kontny; Anne-Paule Gimenez-Roqueplo; Alberto Cascon; Mercedes Robledo; José M de Campos; Francien H van Nederveen; Ronald R de Krijger; Nelly Burnichon; José Gaal; Martin A Walter; Kirsten Reschke; Thorsten Wiech; Johannes Weber; Klaus Dieter Rückauer; Pierre Francois Plouin; Vincent Darrouzet; Sophie Giraud; Charis Eng; Hartmut P H Neumann
Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.
The Journal of clinical endocrinology and metabolism 2009;94(6):1938-44.
2009: Giuseppe Opocher; F Boaretto; V Pignataro; S Demattè; M E Cecchini; Zoran Erlic; Francesca Schiavi
The pheochromocytoma and paraganglioma syndrome: founder effects and the PGL 1 syndrome.
Annales d'endocrinologie 2009;70(3):157-60.
2009: Zoran Erlic; Hartmut P H Neumann
When should genetic testing be obtained in a patient with phaeochromocytoma or paraganglioma?
Clinical endocrinology 2009;70(3):354-7.
2009: Zoran Erlic; Hartmut P H Neumann
Familial pheochromocytoma.
Hormones (Athens, Greece) 2009;8(1):29-38.
2008: Mariola Peczkowska; Zoran Erlic; Michael M Hoffmann; Mariusz Furmanek; Jaroslaw Cwikla; Agata Kubaszek; Aleksander Prejbisz; Zbigniew Szutkowski; Andrzej Kawecki; Krzysztof Chojnowski; Anna Lewczuk; Mieczyslaw Litwin; Witold Szyfter; Martin A Walter; Maren Sullivan; Charis Eng; Andrzej Januszewicz; Hartmut P H Neumann
Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1.
The Journal of clinical endocrinology and metabolism 2008;93(12):4818-25.
2008: Hartmut P H Neumann; Zoran Erlic
Maternal transmission of symptomatic disease with SDHD mutation: fact or fiction?
The Journal of clinical endocrinology and metabolism 2008;93(5):1573-5.
2008: Mariola Peczkowska; Alberto Cascon; Aleksander Prejbisz; Agata Kubaszek; B Jarosław Cwikła; Mariusz Furmanek; Zoran Erlic; Charis Eng; Andrzej Januszewicz; Hartmut P H Neumann
Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation.
Nature clinical practice. Endocrinology & metabolism 2008;4(2):111-5.
2007: Hartmut P H Neumann; Alexander O Vortmeyer; Dieter Schmidt; Martin Werner; Zoran Erlic; Alberto Cascon; Birke Bausch; Andrzej Januszewicz; Charis Eng
Evidence of MEN-2 in the original description of classic pheochromocytoma.
The New England journal of medicine 2007;357(13):1311-5.
2006: Francesca Schiavi; Theodoros Savvoukidis; Franco Trabalzini; Franco Grego; Michele Piazza; Pietro Amistà; Serena Demattè; Antonella Del Piano; Maria Enrica Cecchini; Zoran Erlic; Paola De Lazzari; Franco Mantero; Giuseppe Opocher
Paraganglioma syndrome: SDHB, SDHC, and SDHD mutations in head and neck paragangliomas.
Annals of the New York Academy of Sciences 2006;1073():190-7.
2006: Giuseppe Opocher; Francesca Schiavi; Maurizio Iacobone; Antonio Toniato; Sabina Sattarova; Zoran Erlic; Maddalena Martella; Caterina Mian; Isabella Merante Boschin; Laura Zambonin; Paola De Lazzari; Alessandra Murgia; Maria Rosa Pelizzo; Gennaro Favia; Franco Mantero
Familial nonsyndromic pheochromocytoma.
Annals of the New York Academy of Sciences 2006;1073():149-55.