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Metastatic Pheochromocytoma/Paraganglioma Related to Primary Tumor Development in Childhood or Adolescence: Significant Link to SDHB Mutations

Journal of clinical oncology, 2011-11, Vol.29 (31), p.4137-4142

2011

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Superiority of Fluorodeoxyglucose Positron Emission Tomography to Other Functional Imaging Techniques in the Evaluation of Metastatic SDHB-Associated Pheochromocytoma and Paraganglioma

Journal of clinical oncology, 2007-06, Vol.25 (16), p.2262-2269

2007

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Plasma Metanephrine for Assessing the Selectivity of Adrenal Venous Sampling

Hypertension (Dallas, Tex. 1979), 2013-12, Vol.62 (6), p.1152-1157

2013

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Age at Diagnosis of Pheochromocytoma Differs According to Catecholamine Phenotype and Tumor Location

The journal of clinical endocrinology and metabolism, 2011-02, Vol.96 (2), p.375-384

2011

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Use of 6-[18F]-fluorodopamine positron emission tomography (PET) as first-line investigation for the diagnosis and localization of non-metastatic and metastatic phaeochromocytoma (PHEO)

Clinical endocrinology (Oxford), 2009-07, Vol.71 (1), p.11-17

2009

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Pheochromocytoma crisis induced by glucocorticoids: a report of four cases and review of the literature

European journal of endocrinology, 2008-03, Vol.158 (3), p.423

2008

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Phaeochromocytoma

The Lancet (British edition), 2005-08, Vol.366 (9486), p.665-675

2005

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Clinical review : Current treatment of malignant pheochromocytoma

The journal of clinical endocrinology and metabolism, 2007-04, Vol.92 (4), p.1217-1225

2007

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

JNCI : Journal of the National Cancer Institute, 2012-05, Vol.104 (9), p.700-708

2012

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The Importance of Adrenocortical Glucocorticoids for Adrenomedullary and Physiological Response to Stress: A Study in Isolated Glucocorticoid Deficiency

The journal of clinical endocrinology and metabolism, 2001-12, Vol.86 (12), p.5920-5924

2001

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Biochemical diagnosis of phaeochromocytoma using plasma-free normetanephrine, metanephrine and methoxytyramine: importance of supine sampling under fasting conditions

Clinical endocrinology (Oxford), 2014-04, Vol.80 (4), p.478-486

2014

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Neuropeptide Y expression in phaeochromocytomas: relative absence in tumours from patients with von Hippel–Lindau syndrome

Journal of endocrinology, 2007-05, Vol.193 (2), p.225-233

2007

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MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Clinical cancer research, 2012-05, Vol.18 (10), p.2828-2837

2012

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Biochemical diagnosis of pheochromocytoma: which test is best?

JAMA : the journal of the American Medical Association, 2002-03, Vol.287 (11), p.1427

2002

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Opposing effects of HIF1α and HIF2α on chromaffin cell phenotypic features and tumor cell proliferation: Insights from MYC‐associated factor X

International journal of cancer, 2014-11, Vol.135 (9), p.2054-2064

2014

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Clinical Presentations, Biochemical Phenotypes, and Genotype-Phenotype Correlations in Patients with Succinate Dehydrogenase Subunit B-Associated Pheochromocytomas and Paragangliomas

The journal of clinical endocrinology and metabolism, 2007-03, Vol.92 (3), p.779-786

2007

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Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma

Clinical cancer research, 2013-07, Vol.19 (14), p.3787-3795

2013

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Adverse drug reactions in patients with phaeochromocytoma : Incidence, prevention and management

Drug safety, 2007-01, Vol.30 (11), p.1031-1062

2007

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Seasonal variation in plasma free normetanephrine concentrations: implications for biochemical diagnosis of pheochromocytoma

European journal of endocrinology, 2014-03, Vol.170 (3), p.349

2014

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Children with classic congenital adrenal hyperplasia have elevated serum leptin concentrations and insulin resistance: Potential clinical implications

The journal of clinical endocrinology and metabolism, 2002-05, Vol.87 (5), p.2114-2120

2002

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The role of 6-[18F]fluorodopamine positron emission tomography in the localization of adrenal pheochromocytoma associated with von Hippel-Lindau syndrome

European journal of endocrinology, 2007-04, Vol.156 (4), p.483

2007

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Plasma-free vs deconjugated metanephrines for diagnosis of phaeochromocytoma

Clinical endocrinology (Oxford), 2013-10, Vol.79 (4), p.476-483

2013

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Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glycemic Control during Prolonged Moderate-Intensity Exercise

The journal of clinical endocrinology and metabolism, 2007-08, Vol.92 (8), p.3019-3024

2007

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Candidate Genes Associated With Malignant Pheochromocytomas by Genome-Wide Expression Profiling

Annals of surgery, 2009-12, Vol.250 (6), p.983-990

2009

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Adrenomedullary Dysplasia and Hypofunction in Patients with Classic 21-Hydroxylase Deficiency

The New England journal of medicine, 2000-11, Vol.343 (19), p.1362-1368

2000

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Metastatic Pheochromocytoma/Paraganglioma Related to Primary Tumor Development in Childhood or Adolescence: Significant Link to SDHB Mutations

Superiority of Fluorodeoxyglucose Positron Emission Tomography to Other Functional Imaging Techniques in the Evaluation of Metastatic SDHB-Associated Pheochromocytoma and Paraganglioma

Plasma Metanephrine for Assessing the Selectivity of Adrenal Venous Sampling

Age at Diagnosis of Pheochromocytoma Differs According to Catecholamine Phenotype and Tumor Location

Use of 6-[18F]-fluorodopamine positron emission tomography (PET) as first-line investigation for the diagnosis and localization of non-metastatic and metastatic phaeochromocytoma (PHEO)

Pheochromocytoma crisis induced by glucocorticoids: a report of four cases and review of the literature

Phaeochromocytoma

Clinical review : Current treatment of malignant pheochromocytoma

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

The Importance of Adrenocortical Glucocorticoids for Adrenomedullary and Physiological Response to Stress: A Study in Isolated Glucocorticoid Deficiency

Biochemical diagnosis of phaeochromocytoma using plasma-free normetanephrine, metanephrine and methoxytyramine: importance of supine sampling under fasting conditions

Neuropeptide Y expression in phaeochromocytomas: relative absence in tumours from patients with von Hippel–Lindau syndrome

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Biochemical diagnosis of pheochromocytoma: which test is best?

Opposing effects of HIF1α and HIF2α on chromaffin cell phenotypic features and tumor cell proliferation: Insights from MYC‐associated factor X

Clinical Presentations, Biochemical Phenotypes, and Genotype-Phenotype Correlations in Patients with Succinate Dehydrogenase Subunit B-Associated Pheochromocytomas and Paragangliomas

Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma

Adverse drug reactions in patients with phaeochromocytoma : Incidence, prevention and management

Seasonal variation in plasma free normetanephrine concentrations: implications for biochemical diagnosis of pheochromocytoma

Children with classic congenital adrenal hyperplasia have elevated serum leptin concentrations and insulin resistance: Potential clinical implications

The role of 6-[18F]fluorodopamine positron emission tomography in the localization of adrenal pheochromocytoma associated with von Hippel-Lindau syndrome

Plasma-free vs deconjugated metanephrines for diagnosis of phaeochromocytoma

Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glycemic Control during Prolonged Moderate-Intensity Exercise

Candidate Genes Associated With Malignant Pheochromocytomas by Genome-Wide Expression Profiling

Adrenomedullary Dysplasia and Hypofunction in Patients with Classic 21-Hydroxylase Deficiency

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