Hartmut P H Neumann
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients
Erlic Z, Fottner C, Forrer F, Plöckinger U, Petersenn S, Zabolotny D, Kollukch O, Yaremchuk S, Januszewicz A, Walz M, Eng C, Neumann H, Klose S, Opocher G, Rybicki L, Peçzkowska M, Golcher H, Kann P, Brauckhoff M, Müssig K, Muresan M, Schäffler A, Reisch N, Schott M, Fassnacht M, European-American Pheochromocytoma Study Group. Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients. Clin Cancer Res 2009; 15:6378-85.
Oct 13, 2009Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients
Oct 13, 2009Clin Cancer Res 2009; 15:6378-85
Erlic Zoran, Fottner Christian, Forrer Flavio, Plöckinger Ursula, Petersenn Stephan, Zabolotny Dimitry, Kollukch Oleg, Yaremchuk Svetlana, Januszewicz Andrzej, Walz Martin K, Eng Charis, Neumann Hartmut P H, Klose Silke, Opocher Giuseppe, Rybicki Lisa, Peçzkowska Mariola, Golcher Henriette, Kann Peter H, Brauckhoff Michael, Müssig Karsten, Muresan Michaela, Schäffler Andreas, Reisch Nicole, Schott Matthias, Fassnacht Martin, European-American Pheochromocytoma Study Group
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene
Schiavi F, Välimäki M, Kawecki A, Szutkowski Z, Schipper J, Walz M, Pigny P, Bauters C, Willet-Brozick J, Baysal B, Januszewicz A, Eng C, Opocher G, Neumann H, Forrer F, Walter M, Boedeker C, Bausch B, Peçzkowska M, Gomez C, Strassburg T, Pawlu C, Buchta M, Salzmann M, Hoffmann M, Berlis A, Brink I, Cybulla M, Muresan M, European-American Paraganglioma Study Group. Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. JAMA 2005; 294:2057-63.
Oct 26, 2005Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene
Oct 26, 2005JAMA 2005; 294:2057-63
Schiavi Francesca, Välimäki Matti, Kawecki Andrzej, Szutkowski Zbigniew, Schipper Jörg, Walz Martin K, Pigny Pascal, Bauters Catherine, Willet-Brozick Joan E, Baysal Bora E, Januszewicz Andrzej, Eng Charis, Opocher Giuseppe, Neumann Hartmut P H, Forrer Flavio, Walter Martin A, Boedeker Carsten C, Bausch Birke, Peçzkowska Mariola, Gomez Clara Fuentes, Strassburg Thomas, Pawlu Christian, Buchta Mary, Salzmann Maren, Hoffmann Michael M, Berlis Ansgar, Brink Ingo, Cybulla Markus, Muresan Mihaela, European-American Paraganglioma Study Group
Von Hippel-Lindau disease--a rare disease important to recognize
Jörger M, Köberle D, Neumann H, Gillessen Sommer S. Von Hippel-Lindau disease--a rare disease important to recognize. Onkologie 2005; 28:159-63.
Mar 1, 2005Von Hippel-Lindau disease--a rare disease important to recognize
Mar 1, 2005Onkologie 2005; 28:159-63
Jörger Markus, Köberle Dieter, Neumann Hartmut P H, Gillessen Sommer Silke
Germ-line mutations in nonsyndromic pheochromocytoma
Neumann H, Apel T, Treier M, Reineke M, Walz M, Hoang-Vu C, Brauckhoff M, Klein-Franke A, Klose P, Schmidt H, Maier M, Peçzkowska M, Szmigielski C, Glaesker S, Manz T, Munk R, Bausch B, McWhinney S, Bender B, Gimm O, Franke G, Schipper J, Klisch J, Altehoefer C, Zerres K, Januszewicz A, Eng C, Smith W, Freiburg-Warsaw-Columbus Pheochromocytoma Study Group. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 2002; 346:1459-66.
May 9, 2002Germ-line mutations in nonsyndromic pheochromocytoma
May 9, 2002N Engl J Med 2002; 346:1459-66
Neumann Hartmut P H, Apel Thomas W, Treier Markus, Reineke Martin, Walz Martin K, Hoang-Vu Cuong, Brauckhoff Michael, Klein-Franke Andreas, Klose Peter, Schmidt Heinrich, Maier Margarete, Peçzkowska Mariola, Szmigielski Cesary, Glaesker Sven, Manz Tanja, Munk Robin, Bausch Birke, McWhinney Sarah R, Bender Bernhard U, Gimm Oliver, Franke Gerlind, Schipper Joerg, Klisch Joachim, Altehoefer Carsten, Zerres Klaus, Januszewicz Andrzej, Eng Charis, Smith Wendy M, Freiburg-Warsaw-Columbus Pheochromocytoma Study Group