Clinical and biochemical features of sporadic and hereditary phaeochromocytomas: an analysis of 41 cases investigated in a single endocrine centre-Reference-Cited by-同舟云学术

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Clinical and biochemical features of sporadic and hereditary phaeochromocytomas: an analysis of 41 cases investigated in a single endocrine centre

Published:2004-10 Issue:5 Volume:13 Page:403-409
ISSN:0959-8278
Container-title:European Journal of Cancer Prevention
language:en
Short-container-title:European Journal of Cancer Prevention

Author:

Patócs A,Karádi É,Tóth M,Varga I,Szücs N,Balogh K,Majnik J,Gláz E,Rácz K

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cancer Research,Public Health, Environmental and Occupational Health,Oncology,Epidemiology

Reference38 articles.

1. Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma

2. Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma

3. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas

4. CONSENSUS: Guidelines for Diagnosis and Therapy of MEN Type 1 and Type 2

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1. An Unexpected Death Due to a Subclinical Pheochromocytoma After an Induced Abortion;American Journal of Forensic Medicine & Pathology;2022-06-09

2. Genitourinary Pathology (Including Adrenal Gland);Oncological Surgical Pathology;2020

3. Does this patient have pheochromocytoma? A systematic review of clinical signs and symptoms;J DIABETES METAB DIS;2016

4. Does this patient have Pheochromocytoma? a systematic review of clinical signs and symptoms;Journal of Diabetes & Metabolic Disorders;2016-03-17

5. Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome;Pathology & Oncology Research;2016-03-09

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