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1. Full Text Phaeochromocytoma
by Lenders, Jacques WM and Eisenhofer, Graeme and Mannelli, Massimo and Pacak, Karel
The Lancet, ISSN 0140-6736, 2005, Volume 366, Issue 9486, pp. 665 - 675
Phaeochromocytomas are rare neuroendocrine tumours with a highly variable clinical presentation but most commonly presenting with episodes of headaches,... 
MEDICINE, GENERAL & INTERNAL | POSITRON-EMISSION-TOMOGRAPHY | ADRENAL-SPARING SURGERY | LAPAROSCOPIC ADRENALECTOMY | HEREDITARY PHEOCHROMOCYTOMA | EXTRAADRENAL PHEOCHROMOCYTOMA | MALIGNANT PHEOCHROMOCYTOMA | HIPPEL-LINDAU-DISEASE | CHROMOGRANIN-A | ENDOCRINE NEOPLASIA TYPE-2 | PLASMA METANEPHRINES | Pheochromocytoma - genetics | Pheochromocytoma - diagnosis | Pheochromocytoma - therapy | Humans | Causes of | Care and treatment | Pheochromocytoma | Diagnosis | Risk factors | Pathology | Adrenal glands | Medical treatment | Surgery | Diagnostic tests | Tumors
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2. Full Text Subclinical phaeochromocytoma
by Mannelli, Massimo, M.D and Lenders, Jacques W.M., M.D., PhD and Pacak, Karel, M.D., PhD and Parenti, Gabriele, M.D., PhD and Eisenhofer, Graeme, PhD
Best Practice & Research Clinical Endocrinology & Metabolism, ISSN 1521-690X, 2011, Volume 26, Issue 4, pp. 507 - 515
Phaeochromocytomas and paragangliomas are neural crest-derived tumours. Autopsy studies indicate that relatively large numbers of these tumours remain... 
Endocrinology & Metabolism | subclinical | catecholamines | susceptibility genes | incidentalomas | phaeochromocytoma | malignant | paraganglioma | GENE-MUTATIONS | SYMPATHETIC ACTIVITY | SUSCEPTIBILITY | ENDOCRINE NEOPLASIA TYPE-2 | IDENTIFICATION | SUCCINATE-DEHYDROGENASE | HEREDITARY | ENDOCRINOLOGY & METABOLISM | DOPAMINE | PARAGANGLIOMAS | RECEPTORS | Adrenal Gland Neoplasms - secretion | Catecholamines - secretion | Humans | Pheochromocytoma - pathology | Pheochromocytoma - genetics | Adrenal Gland Neoplasms - genetics | Adrenal Gland Neoplasms - pathology | Pheochromocytoma - secretion | Hypertension | Catecholamines | Disease susceptibility | Peptides | Tumors | Phaeochromocytoma
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3. Full Text Pheochromocytoma: A review
by Tsirlin, A and Oo, Y and Sharma, R and Kansara, A and Gliwa, A and Banerji, M.A
Maturitas, ISSN 0378-5122, 2014, Volume 77, Issue 3, pp. 229 - 238
Abstract Pheochromocytomas are catecholamine producing neuroendocrine tumors that can be adrenal or extra-adrenal in origin. The classic symptoms of... 
Internal Medicine | Obstetrics and Gynecology | Paraganglioma | Catecholamines | Pheochromocytoma | Adrenal gland | METASTATIC PHEOCHROMOCYTOMA | MANAGEMENT | HIPPEL-LINDAU-DISEASE | ENDOCRINE NEOPLASIA TYPE-2 | SECONDARY HYPERTENSION | CALCIUM-CHANNEL BLOCKERS | BIOCHEMICAL-DIAGNOSIS | GERIATRICS & GERONTOLOGY | OBSTETRICS & GYNECOLOGY | ADRENAL PHEOCHROMOCYTOMA | HEREDITARY PARAGANGLIOMA | NEUROFIBROMATOSIS TYPE-1 | Paraganglioma - therapy | Paraganglioma - genetics | Pheochromocytoma - diagnosis | Humans | Male | Paraganglioma - complications | Paraganglioma - diagnosis | Syndrome | Adrenal Gland Neoplasms - diagnosis | Pheochromocytoma - complications | Adrenal Gland Neoplasms - complications | Female | Pheochromocytoma - genetics | Mutation | Adrenal Gland Neoplasms - genetics | Pheochromocytoma - therapy | Adrenal Gland Neoplasms - therapy | Catecholamines - genetics
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4. Full Text Pheochromocytoma and Paraganglioma: An Endocrine Society Clinical Practice Guideline
by Lenders, Jacques W. M and Duh, Quan-Yang and Eisenhofer, Graeme and Gimenez-Roqueplo, Anne-Paule and Grebe, Stefan K. G and Murad, Mohammad Hassan and Naruse, Mitsuhide and Pacak, Karel and Young, William F and Endocrine Society
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 06/2014, Volume 99, Issue 6, pp. 1915 - 1942
Objective: The aim was to formulate clinical practice guidelines for pheochromocytoma and paraganglioma (PPGL). Participants: The Task Force included a chair... 
POSITRON-EMISSION-TOMOGRAPHY | GENOTYPE-PHENOTYPE CORRELATIONS | HIPPEL-LINDAU-SYNDROME | ENDOCRINOLOGY & METABOLISM | TUMOR-SUPPRESSOR GENE | DIFFERENT HEREDITARY FORMS | PLASMA-FREE METANEPHRINES | TANDEM MASS-SPECTROMETRY | NON-SYNDROMIC PHEOCHROMOCYTOMA | CALCIUM-CHANNEL BLOCKERS | URINARY FREE METANEPHRINES | Diagnostic Techniques, Endocrine - standards | Paraganglioma - therapy | Precision Medicine - standards | Pheochromocytoma - diagnosis | Humans | Combined Modality Therapy | Paraganglioma - diagnosis | Evidence-Based Medicine | Diagnostic Imaging - standards | Consensus | Endocrinology - standards | Adrenal Gland Neoplasms - diagnosis | Diagnostic Imaging - methods | Adrenal Gland Neoplasms - epidemiology | Adrenalectomy - methods | Perioperative Care - methods | Perioperative Care - standards | Paraganglioma - epidemiology | Pheochromocytoma - therapy | Adrenal Gland Neoplasms - therapy | Pheochromocytoma - epidemiology
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5. Full Text Laboratory evaluation of pheochromocytoma and paraganglioma
by Eisenhofer, Graeme and Eisenhofer, Graeme and Eisenhofer, Graeme and Peitzsch, Mirko and Peitzsch, Mirko
Clinical chemistry, ISSN 0009-9147, 12/2014, Volume 60, Issue 12, pp. 1486 - 1499
BACKGROUND: Pheochromocytomas and paragangliomas (PPGLs) are potentially lethal yet usually surgically curable causes of endocrine hypertension; therefore,... 
FREE UNCONJUGATED METADRENALINES | ELECTROCHEMICAL DETECTION | LIQUID-CHROMATOGRAPHY | MULTIPLE ENDOCRINE NEOPLASIA | DIFFERENT HEREDITARY FORMS | FREE NORMETANEPHRINE | MEDICAL LABORATORY TECHNOLOGY | PLASMA-FREE METANEPHRINES | TANDEM MASS-SPECTROMETRY | BIOCHEMICAL-DIAGNOSIS | URINARY FREE METANEPHRINES | Clinical Laboratory Techniques | Pheochromocytoma - diagnosis | Humans | Adrenal Gland Neoplasms - blood | Dopamine - blood | Paraganglioma - diagnosis | Adrenal Gland Neoplasms - urine | Normetanephrine - blood | Paraganglioma - blood | Metanephrine - blood | Adrenal Gland Neoplasms - diagnosis | Dopamine - analogs & derivatives | Pheochromocytoma - blood | Pheochromocytoma | Medical examination | Diagnosis | Research | Analysis | Blood | Physiological aspects | Gliomas
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6. Full Text Germline FH Mutations Presenting With Pheochromocytoma
by Clark, Graeme R and Sciacovelli, Marco and Gaude, Edoardo and Walsh, Diana M and Kirby, Gail and Simpson, Michael A and Trembath, Richard C and Berg, Jonathan N and Woodward, Emma R and Kinning, Esther and Morrison, Patrick J and Frezza, Christian and Maher, Eamonn R
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 10/2014, Volume 99, Issue 10, pp. E2046 - E2050
Context: At least a third of the patients with pheochromocytoma (PCC) or paraganglioma (PGL) harbor an underlying germline mutation in a known PCC/PGL gene.... 
FUMARATE HYDRATASE | MALIGNANT PHEOCHROMOCYTOMAS | GENE | PATHWAY | ENDOCRINOLOGY & METABOLISM | SUCCINATE | HEREDITARY LEIOMYOMATOSIS | PARAGANGLIOMA | CANCER | RENAL-CELL CARCINOMA | Paraganglioma - genetics | Humans | Middle Aged | Child, Preschool | Infant | Male | Fumarate Hydratase - genetics | Mutation, Missense | Young Adult | Adolescent | Age of Onset | Germ-Line Mutation | Female | Pheochromocytoma - genetics | Aged | Adrenal Gland Neoplasms - genetics | Child | Infant, Newborn
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7. Full Text Metastatic pheochromocytoma and paraganglioma
by Angelousi, Anna and Kassi, Evanthia and Zografos, Georgios and Kaltsas, Gregory
European Journal of Clinical Investigation, ISSN 0014-2972, 09/2015, Volume 45, Issue 9, pp. 986 - 997
Background Metastatic pheochromocytomas (PCs) and paragangliomas (PGLs) are rare neuroendocrine tumours with a strong genetic background. Design We searched... 
temozolomide | Metastatic paragangliomas | metastatic pheochromocytomas | SDHB mutation | MIBG | Temozolomide | Metastatic pheochromocytomas | MEDICINE, RESEARCH & EXPERIMENTAL | LOCALIZATION | NEUROENDOCRINE TUMORS | EXTRAADRENAL PARAGANGLIOMAS | MAX MUTATIONS | MEDICINE, GENERAL & INTERNAL | HEREDITARY | MALIGNANT PHEOCHROMOCYTOMA | BENIGN | INHIBITOR SUNITINIB | EXPRESSION | ADRENAL PHEOCHROMOCYTOMAS | 3-Iodobenzylguanidine | Paraganglioma - therapy | Paraganglioma - genetics | Pheochromocytoma - diagnosis | Humans | Tomography, X-Ray Computed | Positron-Emission Tomography | Paraganglioma - diagnosis | Adrenal Gland Neoplasms - diagnosis | Multimodal Imaging | Paraganglioma - secondary | Succinate Dehydrogenase - genetics | Fluorodeoxyglucose F18 | Pheochromocytoma - genetics | Mutation | Pheochromocytoma - secondary | Radiopharmaceuticals | Adrenal Gland Neoplasms - genetics | Pheochromocytoma - therapy | Adrenal Gland Neoplasms - pathology | Adrenal Gland Neoplasms - therapy | Chemotherapy | Metastasis | Cancer
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8. Full Text Germ-Line Mutations in Nonsyndromic Pheochromocytoma
by Neumann, Hartmut P.H and Bausch, Birke and McWhinney, Sarah R and Bender, Bernhard U and Gimm, Oliver and Franke, Gerlind and Schipper, Joerg and Klisch, Joachim and Altehoefer, Carsten and Zerres, Klaus and Januszewicz, Andrzej and Smith, Wendy M and Munk, Robin and Manz, Tanja and Glaesker, Sven and Apel, Thomas W and Treier, Markus and Reineke, Martin and Walz, Martin K and Hoang-Vu, Cuong and Brauckhoff, Michael and Klein-Franke, Andreas and Klose, Peter and Schmidt, Heinrich and Maier-Woelfle, Margarete and Peçzkowska, Mariola and Szmigielski, Cesary and Eng, Charis and Freiburg-Warsaw-Columbus Pheochromoc and Freiburg-Warsaw-Columbus Pheochromocytoma Study Group
The New England Journal of Medicine, ISSN 0028-4793, 05/2002, Volume 346, Issue 19, pp. 1459 - 1466
Germ-line mutations are common in familial glomus tumors, which include pheochromocytomas and paragangliomas. This study examined whether unsuspected germ-line... 
MEDICINE, GENERAL & INTERNAL | HIPPEL-LINDAU DISEASE | HEREDITARY PARAGANGLIOMAS | TUMOR-SUPPRESSOR GENE | FAMILIAL PARAGANGLIOMA | ENDOCRINE NEOPLASIA TYPE-2 | MEDULLARY-THYROID CARCINOMA | COMPLEX-II GENE | VHL | SDHD | RET PROTOONCOGENE | Protein Subunits | Glomus Tumor - genetics | Humans | Ligases - genetics | Middle Aged | Child, Preschool | Iron-Sulfur Proteins - genetics | Male | Mutation, Missense | Electron Transport Complex II | Aged, 80 and over | Germ-Line Mutation | Adult | Female | Proto-Oncogene Proteins c-ret | Child | Drosophila Proteins | Oxidoreductases - genetics | Proto-Oncogene Proteins - genetics | Multienzyme Complexes - genetics | von Hippel-Lindau Disease - genetics | Ubiquitin-Protein Ligases | Succinate Dehydrogenase - genetics | Receptor Protein-Tyrosine Kinases - genetics | Adolescent | Age of Onset | Heterozygote | Pheochromocytoma - genetics | Aged | Von Hippel-Lindau Tumor Suppressor Protein | Multiple Endocrine Neoplasia Type 2a - genetics | Tumor Suppressor Proteins | Cohort Studies | Genetic aspects | Pheochromocytoma | Clinical trials | Mutation | Genes | Tumors
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