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Page 1
New genetics in congenital hypothyroidism.
Stoupa A, Kariyawasam D, Muzza M, de Filippis T, Fugazzola L, Polak M, Persani L, Carré A. Stoupa A, et al. Among authors: de filippis t. Endocrine. 2021 Mar;71(3):696-705. doi: 10.1007/s12020-021-02646-9. Epub 2021 Mar 1. Endocrine. 2021. PMID: 33650047 Review.
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.
Sortilin is a putative postendocytic receptor of thyroglobulin.
Botta R, Lisi S, Pinchera A, Giorgi F, Marcocci C, Taddei AR, Fausto AM, Bernardini N, Ippolito C, Mattii L, Persani L, de Filippis T, Calebiro D, Madsen P, Petersen CM, Marinò M. Botta R, et al. Among authors: de filippis t. Endocrinology. 2009 Jan;150(1):509-18. doi: 10.1210/en.2008-0953. Epub 2008 Aug 7. Endocrinology. 2009. PMID: 18687776
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