The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma, and medullary thyroid cancer - Wikidata - awgldk - TriplyDB

The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma, and medullary thyroid cancer

The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma, and medullary thyroid cancer

http://www.wikidata.org/entity/Q36164034

about

Adrenergic crisis due to pheochromocytoma - practical aspects. A short review Differential expression of cell cycle regulators in CDK5-dependent medullary thyroid carcinoma tumorigenesis Endometrial cancer gene panels: clinical diagnostic vs research germline DNA testing.A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.Urinary bladder paraganglioma presenting as micturition-induced palpitations, dyspnea, and angina.Phase 2 study of everolimus monotherapy in patients with nonfunctioning neuroendocrine tumors or pheochromocytomas/paragangliomas.Role of VEGF-A and its receptors in sporadic and MEN2-associated pheochromocytoma Multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma: an update Molecular markers of paragangliomas/pheochromocytomas Development and application of a novel sensitive immunometric assay for calcitonin in a large cohort of patients with medullary and differentiated thyroid cancer, thyroid nodules, and autoimmune thyroid diseases Simultaneous bilateral laparoscopic adrenalectomy for pheochromocytoma in multiple endocrine neoplasia (MEN) syndrome: Case report with review literature Predictors of hemodynamic instability during surgery for pheochromocytoma Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatment Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.PTPRZ1 regulates calmodulin phosphorylation and tumor progression in small-cell lung carcinoma.Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.Metastatic pheochromocytoma: does the size and age matter?Tumor-suppressor role of Notch3 in medullary thyroid carcinoma revealed by genetic and pharmacological induction.Images of pheochromocytoma in adrenal glands.Endocrine hypertension: An overview on the current etiopathogenesis and management options.Safety and feasibility of laparoscopic resection for large (≥ 6 CM) pheochromocytomas without suspected malignancy.Hereditary medullary thyroid cancer: age-appropriate thyroidectomy improves disease-free survival.Pediatric Medullary Thyroid Carcinoma Urinary and plasma catecholamines and metanephrines in dogs with pheochromocytoma, hypercortisolism, nonadrenal disease and in healthy dogs Are patients with hormonally functional phaeochromocytoma and paraganglioma initially receiving a proper adrenoceptor blockade? A retrospective cohort study.An Extra-adrenal Pheochromocytoma Presenting as Malignant Hypertension-A Report of two cases.Efficacy and Safety of Everolimus in Extrapancreatic Neuroendocrine Tumor: A Comprehensive Review of Literature.New developments in the diagnosis and treatment of thyroid cancer.Current understanding and management of medullary thyroid cancer.Laparoscopic adrenalectomy for pheochromocytoma-does size matter? A single surgeon comparative study.Screening for secondary endocrine hypertension in young patients.Trends in the presentation, treatment, and survival of patients with medullary thyroid cancer over the past 30 years Protocol for the examination of specimens from patients with pheochromocytomas and extra-adrenal paragangliomas.The effect of extent of surgery and number of lymph node metastases on overall survival in patients with medullary thyroid cancer.Functional paraganglioma From Bad to Worse: Paraganglioma Diagnosis during Induction of Labor for Coexisting Preeclampsia.Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.Pheochromocytomas and paragangliomas: assessment of malignant potential.Pharmacotherapy options for advanced thyroid cancer: a systematic review.Occult primary medullary thyroid carcinoma presenting with pituitary and parotid metastases: case report and review of the literature.

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The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma, and medullary thyroid cancer

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Aaron I Vinik

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Herbert Chen

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M Sue O'Dorisio

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North American Neuroendocrine Tumor Society (NANETS)

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Rebecca S Sippel

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Ricardo V Lloyd

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P2860

The role of human achaete-scute homolog-1 in medullary thyroid cancer cells

Biochemical diagnosis of pheochromocytoma: which test is best?

High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing

[(123)I]metaiodobenzylguanidine and [(111)In]octreotide uptake in begnign and malignant pheochromocytomas.

Hereditary endocrinopathies.

Valproic acid activates Notch1 signaling and induces apoptosis in medullary thyroid cancer cells

The perioperative management of children with phaeochromocytoma.

Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis.

Guidelines for diagnosis and therapy of MEN type 1 and type 2.

Biochemical diagnosis of pheochromocytoma: how to distinguish true- from false-positive test results.

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