DOI:
10.1055/s-00000025
Hormone and Metabolic Research
Issue 05 ·
Volume 44 ·
May 2012
DOI: 10.1055/s-002-23235
Editorial
Review
Humans, Clinical
334
Lefebvre, S.;
Borson-Chazot, F.;
Boutry-Kryza, N.;
Wion, N.;
Schillo, F.;
Peix, J.-L.;
Brunaud, L.;
Finat, A.;
Calender, A.;
Giraud, S.:
Screening of Mutations in Genes that Predispose to Hereditary Paragangliomas and Pheochromocytomas
343
Eisenhofer, G.;
Vocke, C. D.;
Elkahloun, A.;
Huynh, T.-T.;
Prodanov, T.;
Lenders, J.W. M.;
Timmers, H. J.;
Benhammou, J. N.;
Linehan, W. M.;
Pacak, K.:
Genetic Screening for von Hippel-Lindau Gene Mutations in Non-syndromic Pheochromocytoma: Low Prevalence and False-positives or Misdiagnosis Indicate a Need for Caution
349
Persu, A.;
Lannoy, N.;
Maiter, D.;
Mendola, A.;
Montigny, P.;
Oriot, P.;
Vinck, W.;
Garin, P.;
Hamoir, M.;
Vikkula, M.:
Prevalence and Spectrum of SDHx Mutations in Pheochromocytoma and Paraganglioma in Patients from Belgium: An Update
Review
359
Buffet, A.;
Venisse, A.;
Nau, V.;
Roncellin, I.;
Boccio, V.;
Le Pottier, N.;
Boussion, M.;
Travers, C.;
Simian, C.;
Burnichon, N.;
Abermil, N.;
Favier, J.;
Jeunemaitre, X.;
Gimenez-Roqueplo, A.-P.:
A Decade (2001–2010) of Genetic Testing for Pheochromocytoma and Paraganglioma
Humans, Clinical
379
Zelinka, T.;
Petrák, O.;
Turková, H.;
Holaj, R.;
Štrauch, B.;
Kršek, M.;
Vránková, A. B.;
Musil, Z.;
Dušková, J.;
Kubinyi, J.;
Michalský, D.;
Novák, K.;
Widimský, J.:
High Incidence of Cardiovascular Complications in Pheochromocytoma
Review
Original Basic
Humans, Clinical
411
Zovato, S.;
Kumanova, A.;
Demattè, S.;
Sansovini, M.;
Bodei, L.;
Di Sarra, D.;
Casagranda, E.;
Severi, S.;
Ambrosetti, A.;
Schiavi, F.;
Opocher, G.;
Paganelli, G.:
Peptide Receptor Radionuclide Therapy (PRRT) with 177Lu-DOTATATE in Individuals with Neck or Mediastinal Paraganglioma (PGL)