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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2000 | 1 |
2005 | 1 |
2009 | 1 |
2012 | 2 |
2013 | 1 |
2017 | 1 |
2024 | 0 |
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Page 1
Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
Nat Genet. 2000 Nov;26(3):268-70. doi: 10.1038/81551.
Nat Genet. 2000.
PMID: 11062460
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.
Schiavi F, Boedeker CC, Bausch B, Peçzkowska M, Gomez CF, Strassburg T, Pawlu C, Buchta M, Salzmann M, Hoffmann MM, Berlis A, Brink I, Cybulla M, Muresan M, Walter MA, Forrer F, Välimäki M, Kawecki A, Szutkowski Z, Schipper J, Walz MK, Pigny P, Bauters C, Willet-Brozick JE, Baysal BE, Januszewicz A, Eng C, Opocher G, Neumann HP; European-American Paraganglioma Study Group.
Schiavi F, et al.
JAMA. 2005 Oct 26;294(16):2057-63. doi: 10.1001/jama.294.16.2057.
JAMA. 2005.
PMID: 16249420
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The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
Burnichon N, Rohmer V, Amar L, Herman P, Leboulleux S, Darrouzet V, Niccoli P, Gaillard D, Chabrier G, Chabolle F, Coupier I, Thieblot P, Lecomte P, Bertherat J, Wion-Barbot N, Murat A, Venisse A, Plouin PF, Jeunemaitre X, Gimenez-Roqueplo AP; PGL.NET network.
Burnichon N, et al.
J Clin Endocrinol Metab. 2009 Aug;94(8):2817-27. doi: 10.1210/jc.2008-2504. Epub 2009 May 19.
J Clin Endocrinol Metab. 2009.
PMID: 19454582
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Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3.
Malinoc A, Sullivan M, Wiech T, Schmid KW, Jilg C, Straeter J, Deger S, Hoffmann MM, Bosse A, Rasp G, Eng C, Neumann HP.
Malinoc A, et al.
Endocr Relat Cancer. 2012 May 3;19(3):283-90. doi: 10.1530/ERC-11-0324. Print 2012 Jun.
Endocr Relat Cancer. 2012.
PMID: 22351710
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Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
Lefebvre S, Borson-Chazot F, Boutry-Kryza N, Wion N, Schillo F, Peix JL, Brunaud L, Finat A, Calender A, Giraud S.
Lefebvre S, et al.
Horm Metab Res. 2012 May;44(5):334-8. doi: 10.1055/s-0032-1306308. Epub 2012 Apr 19.
Horm Metab Res. 2012.
PMID: 22517554
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Immunohistochemical loss of succinate dehydrogenase subunit A (SDHA) in gastrointestinal stromal tumors (GISTs) signals SDHA germline mutation.
Miettinen M, Killian JK, Wang ZF, Lasota J, Lau C, Jones L, Walker R, Pineda M, Zhu YJ, Kim SY, Helman L, Meltzer P.
Miettinen M, et al.
Am J Surg Pathol. 2013 Feb;37(2):234-40. doi: 10.1097/PAS.0b013e3182671178.
Am J Surg Pathol. 2013.
PMID: 23282968
Free PMC article.
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Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.
Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group; Topper S.
Nykamp K, et al.
Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11.
Genet Med. 2017.
PMID: 28492532
Free PMC article.
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