Development and external validation of clinical prediction models for pituitary surgery von Zanier, O., Zoli, M., Staartjes, V.E., Alalfi, M., Guaraldi, F., Asioli, S., Rustici, A., Pasquini, E., Faustini-Fustini, M., Erlic, Z., Hugelshofer, M., Voglis, S., Regli, L., Mazzatenta, D., Serra, C.

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Neurofibromatosis type 1: should we screen for other genetic syndromes? A case report of co-existence with multiple endocrine neoplasia 2A von Gkaliagkousi, E., Erlic, Z., Petidis, K., Semertzidis, P., Doumas, M., Zamboulis, C., Neumann, H. P. H., Douma, S.

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12204 Role Of [18F]FDG-PET/CT In Detection Of Immunotherapy-induced Hypophysitis - A Case-control Study von Fischer, A, Martinez Gomez, J M, Mangana, J, Dummer, R, Erlic, Z, Nölting, S, Beuschlein, F, Maurer, A, Messerli, M, Huellner, M W, Skawran, S

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The pheochromocytoma and paraganglioma syndrome: Founder effects and the PGL 1 syndrome von Opocher, G, Boaretto, F, Pignataro, V, Demattè, S, Cecchini, M.E, Erlic, Z, Schiavi, F

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Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome von Erlic, Z, Hoffmann, M M, Sullivan, M, Franke, G, Peczkowska, M, Harsch, I, Schott, M, Gabbert, H E, Valimäki, M, Preuss, S F, Hasse-Lazar, K, Waligorski, D, Robledo, M, Januszewicz, A, Eng, C, Neumann, H P H

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Familial Nonsyndromic Pheochromocytoma von OPOCHER, GIUSEPPE, SCHIAVI, FRANCESCA, IACOBONE, MAURIZIO, TONIATO, ANTONIO, SATTAROVA, SABINA, ERLIC, ZORAN, MARTELLA, MADDALENA, MIAN, CATERINA, MERANTE BOSCHIN, ISABELLA, ZAMBONIN, LAURA, DE LAZZARI, PAOLA, MURGIA, ALESSANDRA, PELIZZO, MARIA ROSA, FAVIA, GENNARO, MANTERO, FRANCO

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Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome von Sullivan, M, Erlic, Z, Hoffmann, M M, Arbeiter, K, Patzer, L, Budde, K, Hoppe, B, Zeier, M, Lhotta, K, Rybicki, L A, Bock, A, Berisha, G, Neumann, H P H

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The pheochromocytoma and paraganglioma syndrome: Founder effects and the PGL 1 syndrome von OPOCHER, G, BOARETTO, F, PIGNATARO, V, DEMATTE, S, CECCHINI, M. E, ERLIC, Z, SCHIAVI, F

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Pheocromocytoma/Paraganglioma Syndrome: SDHB, SDHC and SDHD Mutations in Head and Neck Paragangliomas von Schiavi, F., Trabalzini, F., Dematt??, S., Del Piano, A., Cecchini, M. E., Savvoukidis, T., Erlic, Z., De Lazzari, P., Giacchetti, G., Mantero, F., Opocher, G.

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Supplementary Material for: Autosomal Dominant Polycystic Kidney Disease: Prevalence of Renal Neoplasias in Surgical Kidney Specimens von Jilg, C.A., Drendel, V., Bacher, J., Pisarski, P., Neeff, H., Drognitz, O., Schwardt, M., Gläsker, S., Malinoc, A., Erlic, Z., Nunez, M., Weber, A., Azurmendi, P., Schultze-Seemann, W., Werner, M., Neumann H.P.H.

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Die von Hippel-Lindau Krankheit im Schwarzwald von Neumann, H P H, Gläsker, S, Erlic, Z

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