Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 1
1988 1
1990 1
1991 2
1992 1
1993 2
1994 1
1998 2
1999 1
2002 1
2005 1
2006 1
2007 1
2010 1
2013 1
2015 1
2016 1
2021 1
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

21 results

Results by year

Filters applied: . Clear all
Page 1
High risk of congenital hypothyroidism in multiple pregnancies.
Olivieri A, Medda E, De Angelis S, Valensise H, De Felice M, Fazzini C, Cascino I, Cordeddu V, Sorcini M, Stazi MA; Study Group for Congenital Hypothyroidism. Olivieri A, et al. Among authors: fazzini c. J Clin Endocrinol Metab. 2007 Aug;92(8):3141-7. doi: 10.1210/jc.2007-0238. Epub 2007 May 8. J Clin Endocrinol Metab. 2007. PMID: 17488789
Risk factors for congenital hypothyroidism: results of a population case-control study (1997-2003).
Medda E, Olivieri A, Stazi MA, Grandolfo ME, Fazzini C, Baserga M, Burroni M, Cacciari E, Calaciura F, Cassio A, Chiovato L, Costa P, Leonardi D, Martucci M, Moschini L, Pagliardini S, Parlato G, Pignero A, Pinchera A, Sala D, Sava L, Stoppioni V, Tancredi F, Valentini F, Vigneri R, Sorcini M. Medda E, et al. Among authors: fazzini c. Eur J Endocrinol. 2005 Dec;153(6):765-73. doi: 10.1530/eje.1.02048. Eur J Endocrinol. 2005. PMID: 16322381
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. Among authors: fazzini c. 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
Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis.
Dentice M, Cordeddu V, Rosica A, Ferrara AM, Santarpia L, Salvatore D, Chiovato L, Perri A, Moschini L, Fazzini C, Olivieri A, Costa P, Stoppioni V, Baserga M, De Felice M, Sorcini M, Fenzi G, Di Lauro R, Tartaglia M, Macchia PE. Dentice M, et al. Among authors: fazzini c. J Clin Endocrinol Metab. 2006 Apr;91(4):1428-33. doi: 10.1210/jc.2005-1350. Epub 2006 Jan 17. J Clin Endocrinol Metab. 2006. PMID: 16418214
21 results