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Items: 11

1.

Functioning Mediastinal Paraganglioma Associated with a Germline Mutation of von Hippel-Lindau Gene.

Bahougne T, Romanet P, Mohamed A, Caselles K, Cuny T, Barlier A, Niccoli P.

J Clin Med. 2018 May 23;7(6). pii: E116. doi: 10.3390/jcm7060116.

2.

Primary mediastinal paraganglioma associated with a familial variant in the succinate dehydrogenase B subunit gene.

Samuel N, Ejaz R, Silver J, Ezzat S, Cusimano RJ, Kim RH.

J Surg Oncol. 2018 Feb;117(2):160-162. doi: 10.1002/jso.24818. Epub 2017 Sep 10.

PMID:
28891197
3.

Soft tissue metastasis of mediastinal non-functioning paraganglioma with unusual TTF-1 expression: a potential diagnostic pitfall.

Benej M, Zambo I, Bílek O, Capov I.

Pol J Pathol. 2017;68(4):354-358. doi: 10.5114/pjp.2017.73931.

4.

The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3).

Else T, Marvin ML, Everett JN, Gruber SB, Arts HA, Stoffel EM, Auchus RJ, Raymond VM.

J Clin Endocrinol Metab. 2014 Aug;99(8):E1482-6. doi: 10.1210/jc.2013-3853. Epub 2014 Apr 23.

5.

Phenotypic variability and risk of malignancy in SDHC-linked paragangliomas: lessons from three unrelated cases with an identical germline mutation (p.Arg133*).

Bickmann JK, Sollfrank S, Schad A, Musholt TJ, Springer E, Miederer M, Bartsch O, Papaspyrou K, Koutsimpelas D, Mann WJ, Weber MM, Lackner KJ, Rossmann H, Fottner C.

J Clin Endocrinol Metab. 2014 Mar;99(3):E489-96. doi: 10.1210/jc.2013-3486. Epub 2014 Jan 1.

PMID:
24423348
6.

A novel mutation (P236S) in the succinate dehydrogenase subunit B gene in a Japanese patient with a posterior mediastinal paraganglioma.

Sato H, Shoji S, Kajiwara H, Itoh J, Osamura RY.

Endocr Pathol. 2013 Sep;24(3):144-8. doi: 10.1007/s12022-013-9252-0.

PMID:
23780556
7.

Analysis of pheochromocytomas / paragangliomas from Eastern Slovakia.

Felsoci M, Lazurova I, Wagnerova H, Svajdler M.

Neoplasma. 2013;60(4):452-8. doi: 10.4149/neo_2013_059.

PMID:
23581419
8.

Peptide receptor radionuclide therapy (PRRT) with 177Lu-DOTATATE in individuals with neck or mediastinal paraganglioma (PGL).

Zovato S, Kumanova A, Demattè S, Sansovini M, Bodei L, Di Sarra D, Casagranda E, Severi S, Ambrosetti A, Schiavi F, Opocher G, Paganelli G.

Horm Metab Res. 2012 May;44(5):411-4. doi: 10.1055/s-0032-1311637. Epub 2012 May 7.

PMID:
22566197
9.

Malignant paraganglioma associated with succinate dehydrogenase subunit B in an 8-year-old child: the age of first screening?

Prodanov T, Havekes B, Nathanson KL, Adams KT, Pacak K.

Pediatr Nephrol. 2009 Jun;24(6):1239-42. doi: 10.1007/s00467-008-1111-8. Epub 2009 Feb 3.

10.

Mediastinal paragangliomas: association with mutations in the succinate dehydrogenase genes and aggressive behavior.

Ghayee HK, Havekes B, Corssmit EP, Eisenhofer G, Hammes SR, Ahmad Z, Tessnow A, Lazúrová I, Adams KT, Fojo AT, Pacak K, Auchus RJ.

Endocr Relat Cancer. 2009 Mar;16(1):291-9. doi: 10.1677/ERC-08-0214. Epub 2008 Dec 15.

11.

The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway.

Gimenez-Roqueplo AP, Favier J, Rustin P, Mourad JJ, Plouin PF, Corvol P, Rötig A, Jeunemaitre X.

Am J Hum Genet. 2001 Dec;69(6):1186-97. Epub 2001 Oct 16.

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