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The Journal of Clinical Endocrinology and Metabolism|October 2, 2008
Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1Mariola Peczkowska, Zoran Erlic, Michael M Hoffmann, et al.Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 20, 2007
[Von Hippel-Lindau disease. Interdisciplinary patient care]H P H Neumann, M Cybulla, S Gläsker, et al.Digestive Endoscopy : Official Journal of the Japan Gastroenterological Endoscopy Society|February 20, 2026
Endoscopist and Patients' Values and Preferences on Artificial Intelligence in Endoscopy: An Intercontinental Opinion Survey by the World Endoscopy OrganizationO F Ahmad, A de Groof, A Ali, et al.Cerebrovascular Diseases Extra|November 10, 2012
Characteristics of intracranial aneurysms in the else kröner-fresenius registry of autosomal dominant polycystic kidney diseaseHartmut P H Neumann, Angelica Malinoc, Janina Bacher, et al.Journal of Cancer Research and Clinical Oncology|February 25, 2022
Mismatch repair deficiency, chemotherapy and survival for resectable gastric cancer: an observational study from the German staR cohort and a meta-analysisT Stolze, S Franke, J Haybaeck, et al.American Journal of Human Genetics|December 20, 2003
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paragangliomaSakari Vanharanta, Mary Buchta, Sarah R McWhinney, et al.Endocrine-Related Cancer|September 17, 2008
Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutationIoana N Milos, Karin Frank-Raue, Nelson Wohllk, et al.The Journal of Clinical Endocrinology and Metabolism|March 30, 2012
The endemic paraganglioma syndrome type 1: origin, spread, and clinical expressionFrancesca Schiavi, Serena Demattè, Maria Enrica Cecchini, et al.The World Allergy Organization Journal|December 19, 2024
Ambrosia (ragweed) pollen - A growing aeroallergen of concern in South AfricaDorra Gharbi, Dilys Berman, Frank H Neumann, et al.Annals of Human Genetics|September 13, 2011
Age-related penetrance of hereditary atypical hemolytic uremic syndromeMaren Sullivan, Lisa A Rybicki, Aurelia Winter, et al.Pageof 56