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Page 1
A frequent oligogenic involvement in congenital hypothyroidism.
de Filippis T, Gelmini G, Paraboschi E, Vigone MC, Di Frenna M, Marelli F, Bonomi M, Cassio A, Larizza D, Moro M, Radetti G, Salerno M, Ardissino D, Weber G, Gentilini D, Guizzardi F, Duga S, Persani L. de Filippis T, et al. Hum Mol Genet. 2017 Jul 1;26(13):2507-2514. doi: 10.1093/hmg/ddx145. Hum Mol Genet. 2017. PMID: 28444304 Free article.
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis.
Muzza M, Persani L, de Filippis T, Gastaldi R, Vigone MC, Sala D, Weber G, Lorini R, Beck-Peccoz P, Fugazzola L. Muzza M, et al. Among authors: de filippis t. Clin Endocrinol (Oxf). 2008 Nov;69(5):828-9. doi: 10.1111/j.1365-2265.2008.03265.x. Epub 2008 Apr 10. Clin Endocrinol (Oxf). 2008. PMID: 18410549 No abstract available.
Genetics and phenomics of hypothyroidism due to TSH resistance.
Persani L, Calebiro D, Cordella D, Weber G, Gelmini G, Libri D, de Filippis T, Bonomi M. Persani L, et al. Among authors: de filippis t. Mol Cell Endocrinol. 2010 Jun 30;322(1-2):72-82. doi: 10.1016/j.mce.2010.01.008. Epub 2010 Jan 18. Mol Cell Endocrinol. 2010. PMID: 20083154 Review.
Increased risk for non-autoimmune hypothyroidism in young patients with congenital heart defects.
Passeri E, Frigerio M, De Filippis T, Valaperta R, Capelli P, Costa E, Fugazzola L, Marelli F, Porazzi P, Arcidiacono C, Carminati M, Ambrosi B, Persani L, Corbetta S. Passeri E, et al. Among authors: de filippis t. J Clin Endocrinol Metab. 2011 Jul;96(7):E1115-9. doi: 10.1210/jc.2011-0057. Epub 2011 Apr 27. J Clin Endocrinol Metab. 2011. PMID: 21525159
35 results