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International Journal of Cancer|April 4, 2003
Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomasHilde Dannenberg, Ronald R De Krijger, Erwin van der Harst, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 19, 2005
Clinical characteristics of pheochromocytoma patients with germline mutations in SDHDHilde Dannenberg, Francien H van Nederveen, Mustaffa Abbou, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|June 4, 2019
A next-generation-sequencing panel for mutational analysis of dominant acute hepatic porphyriasJasmin Barman-Aksözen, Lukas Suter, Franziska Wegmann, et al.
The American Journal of Surgical Pathology|February 28, 2008
Islet 1 (Isl1) expression is a reliable marker for pancreatic endocrine tumors and their metastasesAnja M Schmitt, Florian Riniker, Martin Anlauf, et al.
Gastroenterology|May 12, 2005
Precursor lesions in patients with multiple endocrine neoplasia type 1-associated duodenal gastrinomasMartin Anlauf, Aurel Perren, Cora Lu Meyer, et al.
Cancers|June 28, 2019
MiRNAs Are Involved in Tall Cell Morphology in Papillary Thyroid CarcinomaLaura A Boos, Anja Schmitt, Holger Moch, et al.
Endocrine-Related Cancer|August 13, 2010
SDHB loss predicts malignancy in pheochromocytomas/sympathethic paragangliomas, but not through hypoxia signallingAnnika Blank, Anja M Schmitt, Esther Korpershoek, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2004
A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomasMargarete Maier-Woelfle, Michael Brändle, Paul Komminoth, et al.
Endocrine Pathology|January 1, 1995
Molecular Diagnosis of Multiple Endocrine Neoplasia (MEN) in Paraffin-Embedded SpecimensPaul Komminoth, Seraina Muletta-Feurer, Parvin Saremaslani, et al.
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