Head and Neck Paragangliomas in Von Hippel-Lindau Disease and Multiple Endocrine Neoplasia Type 2-Reference-Cited by-同舟云学术

Head and Neck Paragangliomas in Von Hippel-Lindau Disease and Multiple Endocrine Neoplasia Type 2

Published:2009-06-01 Issue:6 Volume:94 Page:1938-1944
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Boedeker Carsten C.¹,Erlic Zoran²,Richard Stéphane³⁴⁵,Kontny Udo⁶,Gimenez-Roqueplo Anne-Paule⁷,Cascon Alberto⁸,Robledo Mercedes⁸,de Campos José M.⁹,van Nederveen Francien H.¹⁰,de Krijger Ronald R.¹⁰,Burnichon Nelly⁷,Gaal José¹⁰,Walter Martin A.¹¹,Reschke Kirsten¹²,Wiech Thorsten¹³,Weber Johannes¹⁴,Rückauer Klaus¹⁵,Plouin Pierre Francois¹⁶,Darrouzet Vincent¹⁷,Giraud Sophie¹⁸,Eng Charis¹⁹,Neumann Hartmut P. H.²

Affiliation:

1. Departments of Otorhinolaryngology (C.C.B.), Albert-Ludwigs-University, D-79106 Freiburg, Germany

2. Department of Nephrology (Z.E., H.P.H.N.), Section of Preventive Medicine, Albert-Ludwigs-University, D-79106 Freiburg, Germany

3. Génétique Oncologique Ecole Pratique des Hautes Estudes-Centre National de la Recherche Scientifique Formation de Recherche en Évolution 2939 (S.R.), F-94270 Kremlin-Bicêtre, France

4. Faculté de Médecine Paris Sud, and Réseau National Institut National du Cancer (INCa) and Centre Pilote Tumeurs Rares INCa (S.R.), F-94270 Kremlin-Bicêtre, France

5. Assistance Publique-Hôpitaux de Paris, Service d’Urologie, Hôpital de Kremlin-Bicêtre (S.R.), F-94270 Kremlin-Bicêtre, France

6. Division of Pediatric Hematology and Oncology (U.K.), Albert-Ludwigs-University, D-79106 Freiburg, Germany

7. Assistance Publique-Hôpitaux de Paris, Service de Génétique (A.-P.G.-R., N.B.), Hôpital Européen Georges Pompidou, and Université Paris Descartes, F-75006 Paris, France

8. Hereditary Endocrine Cancer Group (A.C., M.R.), Spanish National Cancer Center, Madrid, and Instituto de Salud Carlos III Center for Biomedical Research on Rare Diseases (CIBERER), E-28029 Madrid, Spain

9. Neurosurgery Department (J.M.d.C.), Fundación Jiménez Díaz, Autonomous University, E-28049 Madrid, Spain

10. Department of Pathology (F.H.v.N., R.R.d.K., J.G.), Josephine Nefkens Institute, Erasmus MC-University Medical Center Rotterdam, 3000 CA Rotterdam, The Netherlands

11. Department of Nuclear Medicine (M.A.W.), University Hospital Basel, CH-4003 Basel, Switzerland

12. Surgery (K.R.), Albert-Ludwigs-University, D-79106 Freiburg, Germany

13. Pathology (T.W.), Albert-Ludwigs-University, D-79106 Freiburg, Germany

14. Neuroradiology (J.W.), Albert-Ludwigs-University, D-79106 Freiburg, Germany

15. Division of Nephrology and Endocrinology (K.R.), Otto von Guericke University, D-39106 Magdeburg, Germany

16. Unité d’Hypertension artérielle (P.F.P.), Hôpital Européen Georges Pompidou, and Université Paris Descartes, F-75006 Paris, France

17. Department of Otolaryngology (V.D.), Skull Base Surgery Department, Hôpital Pellegrin, University Victor Segalen Bordeaux 2, F-33000 Bordeaux, France

18. Laboratoire de Génétique et Réseau National INCa (S.G.), Hôpital Edouard Herriot, F-69437 Lyon, France

19. Genomic Medicine Institute (C.E.), Lerner Research Institute, and Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio 44195

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/94/6/1938/9063439/jcem1938.pdf

Reference28 articles.

1. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.;Neumann;JAMA,2004

2. Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.;Schiavi;JAMA,2005

3. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.;Baysal;Science,2000

4. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma.;Astuti;Am J Hum Genet,2001

5. Mutations in SDHC cause autosomal dominant paraganglioma, type 3.;Niemann;Nat Genet,2000

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