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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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2001 | 1 |
2007 | 1 |
2012 | 2 |
2013 | 1 |
2024 | 0 |
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Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.
Am J Med Genet. 2001 May 15;100(4):311-4. doi: 10.1002/ajmg.1270.
Am J Med Genet. 2001.
PMID: 11343322
Systematic screening and treatment evaluation of hereditary neck paragangliomas.
Fish JH, Klein-Weigel P, Biebl M, Janecke A, Tauscher T, Fraedrich G.
Fish JH, et al.
Head Neck. 2007 Sep;29(9):864-73. doi: 10.1002/hed.20638.
Head Neck. 2007.
PMID: 17563904
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The endemic paraganglioma syndrome type 1: origin, spread, and clinical expression.
Schiavi F, Demattè S, Cecchini ME, Taschin E, Bobisse S, Del Piano A, Donner D, Barbareschi M, Manera V, Zovato S, Erlic Z, Savvoukidis T, Barollo S, Grego F, Trabalzini F, Amistà P, Grandi C, Branz F, Marroni F, Neumann HP, Opocher G.
Schiavi F, et al.
J Clin Endocrinol Metab. 2012 Apr;97(4):E637-41. doi: 10.1210/jc.2011-2597. Epub 2012 Mar 28.
J Clin Endocrinol Metab. 2012.
PMID: 22456618
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Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome.
Panizza E, Ercolino T, Mori L, Rapizzi E, Castellano M, Opocher G, Ferrero I, Neumann HP, Mannelli M, Goffrini P.
Panizza E, et al.
Hum Mol Genet. 2013 Feb 15;22(4):804-15. doi: 10.1093/hmg/dds487. Epub 2012 Nov 21.
Hum Mol Genet. 2013.
PMID: 23175444
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