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T Kakoi N Rakugi H Ikeda Y Tanabe A Nigawara T 2014 Pathological grading for predicting metastasis in phaeochromocytoma and paraganglioma . Endocrine-Related Cancer 21 405 – 414 . ( https://doi.org/10.1530/ERC-13-0494 ) Kunz PL Reidy
Department of Laboratory Medicine, Department of Radiation Oncology, Department of Endocrinology, Division of Vascular Medicine, Department of Pathology, Department of Pathology, Department of Internal Medicine III, Department of Internal Medicine
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pheochromocytoma . Journal of Clinical Endocrinology and Metabolism 87 4771 – 4774 doi:10.1210/jc.2002-020525 . Gimenez-Roqueplo AP Burnichon N Amar L Favier J Jeunemaitre X Plouin PF 2008 Recent advances in the genetics of phaeochromocytoma
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secretory phenotypes in phaeochromocytoma . Endocrine-Related Cancer 18 97 – 111 . ( https://doi.org/10.1677/ERC-10-0211 ) Elenkova A Matrozova J Vasilev V Robeva R Zacharieva S 2020 Prevalence and progression of carbohydrate disorders
Institute of Pathology, Department of Pathology, Department of Pathology, Department of Urology, Institute of Pathology, Department of Pathology, Klinikum rechts der Isar, Technische Universität München, 81675 Munich, Germany
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Jaap Bonjer H van der Ham F Dinjens WN Lamberts SW de Herder WW Koper JW Stijnen T Proye C 2000 Proliferative index in phaeochromocytomas: does it predict the occurrence of metastases? Journal of Pathology 191 175 – 180 doi:10
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are early genetic events in the development of sporadic pheochromocytomas . American Journal of Pathology 157 353 – 359 . Diaz-Cano SJ de Miguel M Blanes A Tashjian R Galera H Wolfe HJ 2000 Clonal patterns in phaeochromocytomas and
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Allison DJ 1986 Functioning middle mediastinal paraganglioma (phaeochromocytoma) associated with intercarotid paragangliomas . Lancet 1 1061 – 1064 . Eisenhofer G Goldstein DS Sullivan P Csako G Brouwers FM Lai EW Adams KT Pacak
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Department of Pediatric Hematology and Oncology, Service Central de Biophysique et de Médecine Nucléaire, Département d'Oncologie Moléculaire, Program in Reproductive and Adult Endocrinology, 2nd Medical School, Charles University and University Hospital Motol, Prague, Czech Republic
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analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility . Clinical Endocrinology 59 728 – 733 . ( doi:10.1046/j.1365-2265.2003.01914.x ). Astuti D Morris M Krona C Abel F Gentle
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Division of Pathophysiology, National and Kapodistrian University of Athens Medical School, Athens, Greece
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features with noreadrenaline and is used for imaging of phaeochromocytomas, paragangliomas and neuroblastomas ( Jacobson et al. 2010 ). However, 123 I-MIBG scintigraphy has lower sensitivity than SRS for GI-NETs (50%) and pancreatic NETs (<10%) ( Kaltsas
Université de Paris, Paris, France
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Department of Nuclear Medicine, Sorbonne University, Pitie-Salpetriere Hospital, Paris, France
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-0113 ) Bayley JP Kunst HP Cascon A Sampietro ML Gaal J Korpershoek E Hinojar-Gutierrez A Timmers HJ Hoefsloot LH Hermsen MA 2010 SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma . Lancet: Oncology 11 366
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to the intraoperative use in patients with carcinoid associated right-sided heart failure ( Watson et al . 1990 , Vergani et al . 1998 ). Phaeochromocytomas and paragangliomas arise from chromaffin cells and may occur in sporadic or familial forms