Clinical decision making in small non-functioning VHL-related incidentalomas

Autor: Roland Därr, Jonas Kater, Peggy Sekula, Birke Bausch, Tobias Krauss, Christoph Bode, Gerd Walz, Hartmut P Neumann, Stefan Zschiedrich

Publikováno v: Endocrine Connections, Vol 9, Iss 8, Pp 834-844 (2020)

The optimal treatment strategy for patients with small non-functioning VHL-related incidentalomas is unclear. We searched the Freiburg VHL registry for patients with radiologic evidence of pheochromocytoma/paraganglioma (PHEO/PGL). In total, 176 pati

Externí odkaz: https://doaj.org/article/292ad279a5a94b12a1f6b9a78cbc0872

Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literature

Autor: Andreas Ebbehoj, Eleonora P M Corssmit, Jan Calissendorff, Thera P. Links, Özer Makay, Maximilien Rappaport, Petr Vlĕek, Tushar Bandgar, Catharina Larsson, Elena N. Grineva, Luigi Petramala, Ravinder Kaur, Viacheslav I. Egorov, Hartmut P. H. Neumann, Heather Wachtel, Tobias Else, Francesca Boaretto, Xiao-Ping Qi, Henri J L M Timmers, Anna Roslyakova, M. Umit Ugurlu, Ronald M. Lechan, Anand Vaidya, Kornelia Hasse-Lazar, Claudio E. Kater, Esben Søndergaard, Zhi-xian Yu, Rene Eduardo Diaz, Mohammad Hassan Murad, Ruth T Casey, Debbie L. Cohen, Roman Petrov, Lucinda Gruber, C Christofer Juhlin, Claudio Letizia, Maria Adelaide Albergaria Pereira, Inna Stepanovna Kudlai, Bernadette Jenner, Sergiy Cherenko, Lauren Fishbein, William F. Young, Ya-Sheng Huang, Marina Y. Yukina, Scott A Akker, Andrey Y Kovalenko, Uma Kaimal Saikia, Minghao Li, Silvia Rizzati, Stefania Zovato, Xu-dong Fang, Nelson Wohllk, Charis Eng, Mariola Pęczkowska, Martin Fassnacht, Sanjeet Kumar Jaiswal, Oliver Gimm, Gianluca Donatini, Milan Jovanovic, Robin P.F Dullaart, Ilgin Yildirim Simsir, Helen Simpson, Maciej Robaczyk, Marcin Barczyński, Steven G. Waguespack, Katharina Langton, Martin K. Walz, Paul Skierczynski, Alfonso Massimiliano Ferrara, Dipti Sarma, Irina Bancos, Vishnu Garla, Birke Bausch, Maria João Bugalho, Merav Fraenkel, Joanne Ngeow Yuen Yie, Flavia A Costa-Barbosa, Giuseppe Opocher, Camilo Jimenez, Tada Kunavisarut, Larry J. Prokop, Lawrence S Kirschner, Longfei Liu, Feyza Erenler, Elisa Taschin, Valentina Morelli, Per Løgstrup Poulsen, Marcus Quinkler, Natalia Valeryevna Khudiakova, Åse Krogh Rasmussen, Volha Vasilkova, Nicola Tufton, Nikita V. Ivanov, William Drake, Maryna Bobryk, Eric Jonasch, Swati Ramteke-Jadhav, Aviva Cohn, Diane Donegan, Sarka Dvorakova, Elizabeth J. Atkinson, Dmitry Beltsevich, Emma Hodson, Uliana Tsoy, Nino Zavrashvili, Jochen Seufert, Zulfiya Shafigullina, Xin He, Utku E Soyaltin, Nicole M. Iñiguez-Ariza, Timo Deutschbein, Francesca Schiavi, Mark Sherlock, Stefan Zschiedrich, Jes Sloth Mathiesen, Bonita Bennett, Anna Riester, Nalini S. Shah, Giovanni Barbon, Julie A Miller

Publikováno v: Bancos, I, Atkinson, E J, Eng, C, Young, W F, Neumann, H P H & International Pheochromocytoma and Pregnancy Study Group 2021, ' Maternal and fetal outcomes in phaeochromocytoma and pregnancy : a multicentre retrospective cohort study and systematic review of literature ', The Lancet Diabetes & Endocrinology, vol. 9, no. 1, pp. 13-21 . https://doi.org/10.1016/S2213-8587(20)30363-6
Lancet Diabetes & Endocrinology, 9, 1, pp. 13-21
Bancos, I, Atkinson, E, Eng, C, Young, W F, Neumann, H P H, International Pheochromocytoma and Pregnancy Study Group & Robaczyk, M G 2021, ' Maternal and fetal outcomes in phaeochromocytoma and pregnancy : a multicentre retrospective cohort study and systematic review of literature ', The Lancet Diabetes and Endocrinology, vol. 9, no. 1, pp. 13-21 . https://doi.org/10.1016/S2213-8587(20)30363-6
Lancet Diabetes & Endocrinology, 9, 13-21
Lancet Diabetes Endocrinol

Contains fulltext : 245825.pdf (Publisher’s version ) (Closed access) BACKGROUND: Phaeochromocytoma or paraganglioma (collectively known as PPGL) in pregnant women can lead to severe complications and death due to associated catecholamine excess. W

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5323c7add8c398d2a79180450e78b9b
https://hdl.handle.net/2066/245825

Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment

Autor: Cordula A. Jilg, Hansjürgen Agostini, Alexander Puzik, Christine Steiert, Elke Neumann-Haefelin, Sven Gläsker, Horst Urbach, Tobias Krauss, Jan-Helge Klingler, Hartmut P. H. Neumann, Fruzsina Kotsis, Birke Bausch, Jürgen Beck

Publikováno v: Child's Nervous System

Introduction Hemangioblastomas are rare, histologically benign, highly vascularized tumors of the brain, the spinal cord, and the retina, occurring sporadically or associated with the autosomal dominant inherited von Hippel-Lindau (VHL) disease. Chil

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c414149f72d500c4afb9c00b7c98355
https://doi.org/10.1007/s00381-020-04712-5

Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma–paraganglioma

Autor: Birke Bausch, Hartmut P. H. Neumann, Frederik J. Hes, Eleonora P M Corssmit, Johannes A. Rijken, Jeroen C. Jansen, Leonie T. van Hulsteijn, David B. Ascher, Douglas E. V. Pires, Erik F. Hensen, Peter Devilee, Jean-Pierre Bayley

Publikováno v: Bayley, J P, Bausch, B, Rijken, J A, Van Hulsteijn, L T, Jansen, J C, Ascher, D, Pires, D E V, Hes, F J, Hensen, E F, Corssmit, E P M, Devilee, P & Neumann, H P H 2020, ' Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma-paraganglioma ', Journal of Medical Genetics, vol. 57, no. 2, pp. 96-103 . https://doi.org/10.1136/jmedgenet-2019-106214
Journal of Medical Genetics, 57(2), 96-103. BMJ Publishing Group
Journal of Medical Genetics, 57(2), 96-103. BMJ PUBLISHING GROUP

BackgroundPathogenic germline variants in subunits of succinate dehydrogenase (SDHB, SDHC and SDHD) are broadly associated with disease subtypes of phaeochromocytoma–paraganglioma (PPGL) syndrome. Our objective was to investigate the role of varian

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a817ac92ed8d0ec54ace03874bfb4da
https://doi.org/10.1136/jmedgenet-2019-106214

Max Schottelius: Pioneer in Pheochromocytoma

Autor: Hartmut P. H. Neumann, Charis Eng, Birke Bausch, Helena Leijon, Arthur S. Tischler, Kurt Werner Schmid

Publikováno v: Journal of the Endocrine Society

First descriptions of diseases attract tremendous interest because they reveal scientific insight even in retrospect. Max Schottelius, the pathologist contributing the first histological description of pheochromocytoma, remains anonymous. We reviewed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::666f7be68543832a245f6f8a7896c828
https://doi.org/10.1210/js.2017-00208