Renaissance of (18)F-FDG Positron Emission Tomography in the Imaging of Pheochromocytoma/Paraganglioma

Por Taïeb, David, Timmers, Henri J. L. M., Shulkin, Barry L., Pacak, Karel
Publicado em 2014

Clinical aspects of SDHx-related pheochromocytoma and paraganglioma

Por Timmers, Henri J L M, Gimenez-Roqueplo, Anne-Paule, Mannelli, Massimo, Pacak, Karel
Publicado no Endocr Relat Cancer (2009)

Denervation of carotid baro- and chemoreceptors in humans

Por Timmers, Henri J L M, Wieling, Wouter, Karemaker, John M, Lenders, Jacques W M
Publicado em 2003

Use of 6-[18F]-fluorodopamine positron emission tomography as first-line investigation for the diagnosis and localization of non-metastatic and metastatic pheochromocytoma

Por Timmers, Henri J.L.M., Eisenhofer, Graeme, Carrasquillo, Jorge A., Chen, Clara C., Whatley, Millie, Ling, Alexander, Adams, Karen T., Pacak, Karel
Publicado em 2008

Brief Communication: Radiographic Contrast Infusion and Catecholamine Release in Patients With Pheochromocytoma

Por Baid, Smita K., Lai, Edwin W., Wesley, Robert A., Ling, Alex, Timmers, Henri J.L.M., Adams, Karen T., Kozupa, Anna, Pacak, Karel
Publicado em 2009

Biochemically Silent Abdominal Paragangliomas in Patients with Mutations in the Succinate Dehydrogenase Subunit B Gene

Por Timmers, Henri J. L. M., Pacak, Karel, Huynh, Thanh T., Abu-Asab, Mones, Tsokos, Maria, Merino, Maria J., Baysal, Bora E., Adams, Karen T., Eisenhofer, Graeme
Publicado em 2008

Comparison of (18)F-Fluoro-L-DOPA, (18)F-Fluoro-Deoxyglucose, and (18)F-Fluorodopamine PET and (123)I-MIBG Scintigraphy in the Localization of Pheochromocytoma and Paraganglioma

Por Timmers, Henri J. L. M., Chen, Clara C., Carrasquillo, Jorge A., Whatley, Millie, Ling, Alexander, Havekes, Bastiaan, Eisenhofer, Graeme, Martiniova, Lucia, Adams, Karen T., Pacak, Karel
Publicado em 2009

Staging and Functional Characterization of Pheochromocytoma and Paraganglioma by (18)F-Fluorodeoxyglucose ((18)F-FDG) Positron Emission Tomography

Por Timmers, Henri J. L. M., Chen, Clara C., Carrasquillo, Jorge A., Whatley, Millie, Ling, Alexander, Eisenhofer, Graeme, King, Kathryn S., Rao, Jyotsna U., Wesley, Robert A., Adams, Karen T., Pacak, Karel
Publicado em 2012

SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors

Por Renkema, G Herma, Wortmann, Saskia B, Smeets, Roel J, Venselaar, Hanka, Antoine, Marion, Visser, Gepke, Ben-Omran, Tawfeg, van den Heuvel, Lambert P, Timmers, Henri J L M, Smeitink, Jan A, Rodenburg, Richard J T
Publicado no Eur J Hum Genet (2015)

Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas

Por Hoekstra, Attje S., Hensen, Erik F., Jordanova, Ekaterina S., Korpershoek, Esther, Anouk N.A., van der Horst-Schrivers, Cornelisse, Cees, Corssmit, Eleonora P.M., Hes, Frederik J., Jansen, Jeroen C., Kunst, Henricus P.M., Timmers, Henri J.L.M., Bateman, Adrian, Eccles, Diana, Bovée, Judith V.M.G., Devilee, Peter, Bayley, Jean-Pierre
Publicado no Oncotarget (2017)