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Department of Clinical and Experimental Medicine, Department of Surgery, Faculty of Health Sciences, Linköping University, SE-58185 Linköping, Sweden
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Friberg P Grebe SK Timmers HJ 2011b Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma . Endocrine-Related Cancer 18 97 – 111 . ( doi:10.1677/ERC-10-0211 ). Gill AJ Benn DE Chou A Clarkson A Muljono A Meyer
Department of Molecular Medicine and Surgery, Cancer Centre Karolinska, Department of Surgery, Department of Oncology–Pathology, Department of Pathology, Karolinska Institutet, Karolinska University Hospital, CCK R8:04, SE-171 76 Stockholm, Sweden
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Department of Molecular Medicine and Surgery, Cancer Centre Karolinska, Department of Surgery, Department of Oncology–Pathology, Department of Pathology, Karolinska Institutet, Karolinska University Hospital, CCK R8:04, SE-171 76 Stockholm, Sweden
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Department of Molecular Medicine and Surgery, Cancer Centre Karolinska, Department of Surgery, Department of Oncology–Pathology, Department of Pathology, Karolinska Institutet, Karolinska University Hospital, CCK R8:04, SE-171 76 Stockholm, Sweden
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Department of Molecular Medicine and Surgery, Cancer Centre Karolinska, Department of Surgery, Department of Oncology–Pathology, Department of Pathology, Karolinska Institutet, Karolinska University Hospital, CCK R8:04, SE-171 76 Stockholm, Sweden
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dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas . Oncogene 22 1358 – 1364 . ( doi:10.1038/sj.onc.1206300 ). Boedeker C 2011
Program in Reproductive and Adult Endocrinology, Nuclear Medicine Division, Radiology and Imaging Sciences Department, Section of Endocrinology and Metabolism, Medical Oncology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA
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Program in Reproductive and Adult Endocrinology, Nuclear Medicine Division, Radiology and Imaging Sciences Department, Section of Endocrinology and Metabolism, Medical Oncology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA
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K Canizales A Avril N Monson JP Grossman AB Reznek RH 2008 123 I-metaiodobenzylguanidine (MIBG) scintigraphy for the detection of adrenal and extra-adrenal phaeochromocytomas: CT and MRI correlation . Clinical Endocrinology 69 181
Section on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
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secretory phenotypes in phaeochromocytoma . Endocrine-Related Cancer 18 97 – 111 . ( https://doi.org/10.1677/ERC-10-0211 ) Eisenhofer G Lenders JW Siegert G Bornstein SR Friberg P Milosevic D Mannelli M Linehan WM Adams K Timmers HJ , 2012 Plasma
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. Chrisoulidou A Kaltsas G Ilias I Grossman AB 2007 The diagnosis and management of malignant phaeochromocytoma and paraganglioma . Endocrine-Related Cancer 14 569 – 585 . Cleary S Phillips JK Huynh TT Pacak K Elkahloun AG Barb J
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Département de Médecine Génomique des Tumeurs et des Cancers, Fédération de Génétique et de Médecine Génomique, Assistance Publique-Hôpitaux de Paris (AP-HP) Centre, Hôpital Européen Georges Pompidou, Paris, France
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P Plouin PF Jeunemaitre X , et al. 2003 Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas . Cancer Research 63 5615 – 5621 . Hu C-J Wang L-Y Chodosh LA Keith B & Simon MC 2003
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Section on Endocrinology and Genetics (SEGEN), Department of Biophysics and Nuclear Medicine, Faculty of Medicine, Laboratory of Pathology, Section on Medical Neuroendocrinology (SMN), Section of Immunopathology and Laboratory of Immunology, Department of Nuclear Medicine, Institut Paoli‐Calmettes, Emeritus Staff Center, Program on Developmental Endocrinology and Genetics (PDEGEN), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Building 10, CRC, Room 1‐3330, 10 Center Drive, MSC1103, Bethesda, Maryland 20892, USA
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Section on Endocrinology and Genetics (SEGEN), Department of Biophysics and Nuclear Medicine, Faculty of Medicine, Laboratory of Pathology, Section on Medical Neuroendocrinology (SMN), Section of Immunopathology and Laboratory of Immunology, Department of Nuclear Medicine, Institut Paoli‐Calmettes, Emeritus Staff Center, Program on Developmental Endocrinology and Genetics (PDEGEN), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Building 10, CRC, Room 1‐3330, 10 Center Drive, MSC1103, Bethesda, Maryland 20892, USA
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Section on Endocrinology and Genetics (SEGEN), Department of Biophysics and Nuclear Medicine, Faculty of Medicine, Laboratory of Pathology, Section on Medical Neuroendocrinology (SMN), Section of Immunopathology and Laboratory of Immunology, Department of Nuclear Medicine, Institut Paoli‐Calmettes, Emeritus Staff Center, Program on Developmental Endocrinology and Genetics (PDEGEN), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Building 10, CRC, Room 1‐3330, 10 Center Drive, MSC1103, Bethesda, Maryland 20892, USA
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Section on Endocrinology and Genetics (SEGEN), Department of Biophysics and Nuclear Medicine, Faculty of Medicine, Laboratory of Pathology, Section on Medical Neuroendocrinology (SMN), Section of Immunopathology and Laboratory of Immunology, Department of Nuclear Medicine, Institut Paoli‐Calmettes, Emeritus Staff Center, Program on Developmental Endocrinology and Genetics (PDEGEN), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Building 10, CRC, Room 1‐3330, 10 Center Drive, MSC1103, Bethesda, Maryland 20892, USA
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mutation in familial phaeochromocytoma . Lancet 357 1181 – 1182 . ( doi:10.1016/S0140-6736(00)04378-6 ). Baysal BE Ferrell RE Willett-Brozick JE Lawrence EC Myssiorek D Bosch A van der Mey A Taschner PE Rubinstein WS Myers EN
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; Cambridge Laboratories, UK). The presence of phaeochromocytoma and hyperparathyroidism was excluded by appropriate testing, including measurement of urinary catecholamines, ionized calcium and parathyroid hormone (PTH). The patient was thus submitted to
Department of Health Science, Universidad de Alcalá, Madrid, Spain
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Group of Endocrine Disorders, Institut d’Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain
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antihypertensive drugs. The rate of intraoperative complications in our study was 33.3%, but no intraoperative or immediate postsurgical death was reported. Despite the significant reduction in morbidity and mortality of the surgery for phaeochromocytoma over
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V Khau Van Kien P Corvol P Plouin PF Jeunemaitre X 2003 Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas . Cancer Research 63 5615 – 5621 . Grogan RH Mitmaker EJ Duh QY 2011