Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes-Reference-Cited by-同舟云学术

Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes

Published:2013-05-03 Issue:6 Volume:79 Page:817-823
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Pęczkowska Mariola¹,Kowalska Aldona²,Sygut Jacek³,Waligórski Dariusz²,Malinoc Angelica⁴,Janaszek-Sitkowska Hanna¹,Prejbisz Aleksander¹,Januszewicz Andrzej¹,Neumann Hartmut P. H.⁴

Affiliation:

1. Department of Hypertension; Institute of Cardiology; Warsaw Poland

2. Department of Endocrinology and Nuclear Medicine; Holycross Cancer Center; Kielce Poland

3. Department of Pathology and Cancer Biology; Holycross Cancer Center; Kielce Poland

4. Department of Nephrology; Section of Preventive Medicine; Albert-Ludwigs-University of Freiburg; Freiburg Germany

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Reference47 articles.

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2. Germ-line mutations in nonsyndromic pheochromocytoma;Neumann;New England Journal of Medicine,2002

3. Genetic testing in phaeochromocytoma or functional paraganglioma;Amar;Journal of Clinical Oncology,2005

4. Clinically guided genetic screening in a large cohort of Italian patients with phaeochromocytomas and/or functional or nonfunctional paragangliomas;Mannelli;Journal of Clinical Endocrinology and Metabolism,2009

5. Phaeochromocytoma, new genes and screening strategies;Gimenez-Roqueplo;Clinical Endocrinology,2006

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