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Results by year

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

Year Number of Results
1957 1
1958 1
1964 1
1966 1
1968 1
1973 1
1974 1
1978 1
1979 1
1980 2
1981 1
1982 1
1983 5
1985 4
1986 2
1987 9
1988 3
1989 4
1990 5
1991 6
1992 6
1993 1
1994 1
1995 6
1996 5
1997 5
1998 5
1999 7
2000 5
2001 4
2002 3
2003 5
2004 8
2005 8
2006 5
2007 7
2008 7
2009 10
2010 8
2011 14
2012 4
2013 8
2014 10
2015 5
2016 5
2017 4
2018 1
2019 4
2020 2
2021 7
2022 2
Text availability
Article attribute
Article type
Publication date

Search Results

211 results
Results by year
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Page 1
Reply.
Ghaddhab C, Morin C, Brunel-Guitton C, Mitchell GA, Van Vliet G, Huot C. Ghaddhab C, et al. Among authors: van vliet g. J Pediatr. 2017 Aug;187:334-335. doi: 10.1016/j.jpeds.2017.04.067. Epub 2017 May 24. J Pediatr. 2017. PMID: 28550952 No abstract available.
Redefining Congenital Hypothyroidism?
Van Vliet G, Diaz Escagedo P. Van Vliet G, et al. J Clin Endocrinol Metab. 2021 Mar 8;106(3):e1463-e1465. doi: 10.1210/clinem/dgaa905. J Clin Endocrinol Metab. 2021. PMID: 33274373 No abstract available.
European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism.
Léger J, Olivieri A, Donaldson M, Torresani T, Krude H, van Vliet G, Polak M, Butler G; ESPE-PES-SLEP-JSPE-APEG-APPES-ISPAE; Congenital Hypothyroidism Consensus Conference Group. Léger J, et al. Among authors: van vliet g. J Clin Endocrinol Metab. 2014 Feb;99(2):363-84. doi: 10.1210/jc.2013-1891. Epub 2014 Jan 21. J Clin Endocrinol Metab. 2014. PMID: 24446653 Free PMC article.
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.
Miraoui H, Dwyer AA, Sykiotis GP, Plummer L, Chung W, Feng B, Beenken A, Clarke J, Pers TH, Dworzynski P, Keefe K, Niedziela M, Raivio T, Crowley WF Jr, Seminara SB, Quinton R, Hughes VA, Kumanov P, Young J, Yialamas MA, Hall JE, Van Vliet G, Chanoine JP, Rubenstein J, Mohammadi M, Tsai PS, Sidis Y, Lage K, Pitteloud N. Miraoui H, et al. Among authors: van vliet g. Am J Hum Genet. 2013 May 2;92(5):725-43. doi: 10.1016/j.ajhg.2013.04.008. Am J Hum Genet. 2013. PMID: 23643382 Free PMC article.
[Congenital hypothyroidism].
Carranza D, Van Vliet G, Polak M. Carranza D, et al. Among authors: van vliet g. Ann Endocrinol (Paris). 2006 Sep;67(4):295-302. doi: 10.1016/s0003-4266(06)72601-4. Ann Endocrinol (Paris). 2006. PMID: 17072233 Review. French.
Turner's syndrome.
Taback SP, Deal C, Van Vliet G. Taback SP, et al. Among authors: van vliet g. N Engl J Med. 1997 May 22;336(21):1527; author reply 1527-8. N Engl J Med. 1997. PMID: 9157285 No abstract available.
Treatment of congenital hypothyroidism.
Van Vliet G. Van Vliet G. Lancet. 2001 Jul 14;358(9276):86-7. doi: 10.1016/S0140-6736(01)05376-4. Lancet. 2001. PMID: 11463405 Review. No abstract available.
Therapeutic approach of fetal thyroid disorders.
Polak M, Van Vliet G. Polak M, et al. Among authors: van vliet g. Horm Res Paediatr. 2010;74(1):1-5. doi: 10.1159/000297595. Epub 2010 May 7. Horm Res Paediatr. 2010. PMID: 20453471 Free article. Review.
211 results