Cassio A - Search Results

1

Mutational and functional studies on NR5A1 gene in 46,XY disorders of sex development: identification of six novel loss of function mutations.

Rocca MS, Ortolano R, Menabò S, Baronio F, Cassio A, Russo G, Balsamo A, Ferlin A, Baldazzi L. Rocca MS, et al. Among authors: cassio a. Fertil Steril. 2018 Jun;109(6):1105-1113. doi: 10.1016/j.fertnstert.2018.02.123. Fertil Steril. 2018. PMID: 29935645 Free article.

2

Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism.

Olivieri A, Corbetta C, Weber G, Vigone MC, Fazzini C, Medda E; Italian Study Group for Congenital Hypothyroidism. Olivieri A, et al. J Clin Endocrinol Metab. 2013 Apr;98(4):1403-8. doi: 10.1210/jc.2012-3273. Epub 2013 Feb 26. J Clin Endocrinol Metab. 2013. PMID: 23443814

3

Multiple factors influencing the incidence of congenital hypothyroidism detected by neonatal screening.

Olivieri A, Fazzini C, Medda E; Italian Study Group for Congenital Hypothyroidism. Olivieri A, et al. Horm Res Paediatr. 2015;83(2):86-93. doi: 10.1159/000369394. Epub 2015 Jan 6. Horm Res Paediatr. 2015. PMID: 25572470

4

Treatment for congenital hypothyroidism: thyroxine alone or thyroxine plus triiodothyronine?

Cassio A, Cacciari E, Cicognani A, Damiani G, Missiroli G, Corbelli E, Balsamo A, Bal M, Gualandi S. Cassio A, et al. Pediatrics. 2003 May;111(5 Pt 1):1055-60. doi: 10.1542/peds.111.5.1055. Pediatrics. 2003. PMID: 12728088 Clinical Trial.

5

CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency.

Balsamo A, Cicognani A, Baldazzi L, Barbaro M, Baronio F, Gennari M, Bal M, Cassio A, Kontaxaki K, Cacciari E. Balsamo A, et al. Among authors: cassio a. J Clin Endocrinol Metab. 2003 Dec;88(12):5680-8. doi: 10.1210/jc.2003-030123. J Clin Endocrinol Metab. 2003. PMID: 14671153

6

A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism.

Balsamo A, Antelli A, Baldazzi L, Baronio F, Lazareva D, Cassio A, Cicognani A. Balsamo A, et al. Among authors: cassio a. Am J Med Genet A. 2005 Jun 15;135(3):292-6. doi: 10.1002/ajmg.a.30689. Am J Med Genet A. 2005. PMID: 15884018

7

Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults.

Cassio A, Bal MO, Orsini LF, Balsamo A, Sansavini S, Gennari M, De Cristofaro E, Cicognani A. Cassio A, et al. J Pediatr. 2006 Oct;149(4):532-6. doi: 10.1016/j.jpeds.2006.05.026. J Pediatr. 2006. PMID: 17011327 Clinical Trial.

8

Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis.

Corrias A, Cassio A, Weber G, Mussa A, Wasniewska M, Rapa A, Gastaldi R, Einaudi S, Baronio F, Vigone MC, Messina MF, Bal M, Bona G, de Sanctis C; Study Group for Thyroid Diseases of Italian Society for Pediatric Endocrinology and Diabetology (SIEDP/ISPED). Corrias A, et al. Among authors: cassio a. Arch Pediatr Adolesc Med. 2008 Jun;162(6):526-31. doi: 10.1001/archpedi.162.6.526. Arch Pediatr Adolesc Med. 2008. PMID: 18524742

9

Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism.

Nicoletti A, Bal M, De Marco G, Baldazzi L, Agretti P, Menabò S, Ballarini E, Cicognani A, Tonacchera M, Cassio A. Nicoletti A, et al. Among authors: cassio a. J Clin Endocrinol Metab. 2009 Nov;94(11):4187-94. doi: 10.1210/jc.2009-0618. Epub 2009 Oct 9. J Clin Endocrinol Metab. 2009. PMID: 19820021

10

Long-term clinical significance of thyroid autoimmunity in children with celiac disease.

Cassio A, Ricci G, Baronio F, Miniaci A, Bal M, Bigucci B, Conti V, Cicognani A. Cassio A, et al. J Pediatr. 2010 Feb;156(2):292-5. doi: 10.1016/j.jpeds.2009.08.047. Epub 2009 Oct 20. J Pediatr. 2010. PMID: 19846116

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