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Functional Imaging of Endocrine Tumors: Role of Positron Emission Tomography

Endocrine reviews, 2004-08, Vol.25 (4), p.568-580

2004

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Dietary Influences on Plasma and Urinary Metanephrines: Implications for Diagnosis of Catecholamine-Producing Tumors

The journal of clinical endocrinology and metabolism, 2009-08, Vol.94 (8), p.2841-2849

2009

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Biochemical and Clinical Manifestations of Dopamine-Producing Paragangliomas: Utility of Plasma Methoxytyramine

The journal of clinical endocrinology and metabolism, 2005-04, Vol.90 (4), p.2068-2075

2005

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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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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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High Frequency of SDHB Germline Mutations in Patients with Malignant Catecholamine-Producing Paragangliomas: Implications for Genetic Testing

The journal of clinical endocrinology and metabolism, 2006-11, Vol.91 (11), p.4505-4509

2006

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Superiority of 6-[18F]-Fluorodopamine Positron Emission Tomography Versus [131I]-Metaiodobenzylguanidine Scintigraphy in the Localization of Metastatic Pheochromocytoma

The journal of clinical endocrinology and metabolism, 2003-09, Vol.88 (9), p.4083-4087

2003

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

The journal of clinical endocrinology and metabolism, 2008-12, Vol.93 (12), p.4826-4832

2008

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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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Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes

The journal of clinical endocrinology and metabolism, 2001-05, Vol.86 (5), p.1999-2008

2001

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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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Low Sensitivity of Glucagon Provocative Testing for Diagnosis of Pheochromocytoma

The journal of clinical endocrinology and metabolism, 2010-01, Vol.95 (1), p.238-245

2010

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Utility of plasma free metanephrines for detecting childhood pheochromocytoma

The journal of clinical endocrinology and metabolism, 2002-05, Vol.87 (5), p.1955-1960

2002

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Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glucose Elevation in Response to High-Intensity Exercise

The journal of clinical endocrinology and metabolism, 2004-02, Vol.89 (2), p.591-597

2004

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Stress Dose of Hydrocortisone Is Not Beneficial in Patients with Classic Congenital Adrenal Hyperplasia Undergoing Short-Term, High-Intensity Exercise

The journal of clinical endocrinology and metabolism, 2004-08, Vol.89 (8), p.3679-3684

2004

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Mutations associated with succinate dehydrogenase d-related malignant paragangliomas

Clinical endocrinology (Oxford), 2008-04, Vol.68 (4), p.561-566

2008

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Different expression of catecholamine transporters in phaeochromocytomas from patients with von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2

European journal of endocrinology, 2005-10, Vol.153 (4), p.551

2005

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A Pheo lurks : Novel approaches for locating occult pheochromocytoma

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3641-3646

2001

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Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3031-3037

2002

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Lack of leptin suppression in response to hypersecretion of catecholamines in pheochromocytoma patients

Metabolism, clinical and experimental, 1999-05, Vol.48 (5), p.543-545

1999

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Functional Imaging of Endocrine Tumors: Role of Positron Emission Tomography

Dietary Influences on Plasma and Urinary Metanephrines: Implications for Diagnosis of Catecholamine-Producing Tumors

Biochemical and Clinical Manifestations of Dopamine-Producing Paragangliomas: Utility of Plasma Methoxytyramine

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

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

High Frequency of SDHB Germline Mutations in Patients with Malignant Catecholamine-Producing Paragangliomas: Implications for Genetic Testing

Superiority of 6-[18F]-Fluorodopamine Positron Emission Tomography Versus [131I]-Metaiodobenzylguanidine Scintigraphy in the Localization of Metastatic Pheochromocytoma

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

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

Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes

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

Low Sensitivity of Glucagon Provocative Testing for Diagnosis of Pheochromocytoma

Utility of plasma free metanephrines for detecting childhood pheochromocytoma

Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glucose Elevation in Response to High-Intensity Exercise

Stress Dose of Hydrocortisone Is Not Beneficial in Patients with Classic Congenital Adrenal Hyperplasia Undergoing Short-Term, High-Intensity Exercise

Mutations associated with succinate dehydrogenase d-related malignant paragangliomas

Different expression of catecholamine transporters in phaeochromocytomas from patients with von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2

A Pheo lurks : Novel approaches for locating occult pheochromocytoma

Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiency

Lack of leptin suppression in response to hypersecretion of catecholamines in pheochromocytoma patients

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