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

Year Number of Results
1965 1
1966 5
1967 8
1968 7
1969 3
1970 7
1971 7
1972 6
1973 8
1974 7
1975 13
1976 8
1977 3
1978 4
1979 8
1980 5
1981 5
1982 2
1983 9
1984 1
1985 9
1986 12
1987 4
1988 11
1989 3
1990 6
1991 8
1992 5
1993 10
1994 7
1995 13
1996 8
1997 11
1998 7
1999 9
2000 14
2001 9
2002 14
2003 15
2004 9
2005 16
2006 14
2007 18
2008 18
2009 33
2010 22
2011 35
2012 28
2013 27
2014 27
2015 32
2016 32
2017 31
2018 28
2019 20
2020 1
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Article attribute
Article type
Publication date

Search Results

623 results
Results by year
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Page 1
On the Etiology of Molar-Incisor Hypomineralization.
Vieira AR, Kup E. Vieira AR, et al. Caries Res. 2016;50(2):166-9. doi: 10.1159/000445128. Epub 2016 Apr 26. Caries Res. 2016. PMID: 27111773
Weaker dental enamel explains dental decay.
Vieira AR, Gibson CW, Deeley K, Xue H, Li Y. Vieira AR, et al. PLoS One. 2015 Apr 17;10(4):e0124236. doi: 10.1371/journal.pone.0124236. eCollection 2015. PLoS One. 2015. PMID: 25885796 Free PMC article.
[Alteración del gen AMELX en amelogénesis imperfecta. Una breve revisión].
Tremillo-Maldonado O, Molina-Frechero N, González-González R, Bologna-Molina R. Tremillo-Maldonado O, et al. Gac Med Mex. 2019;155(1):101-107. doi: 10.24875/GMM.18003604. Gac Med Mex. 2019. PMID: 30799455 Free article. Review. Spanish.
Loss of Function of Evc2 in Dental Mesenchyme Leads to Hypomorphic Enamel.
Zhang H, Takeda H, Tsuji T, Kamiya N, Kunieda T, Mochida Y, Mishina Y. Zhang H, et al. J Dent Res. 2017 Apr;96(4):421-429. doi: 10.1177/0022034516683674. Epub 2017 Jan 12. J Dent Res. 2017. PMID: 28081373 Free PMC article.
[Oral diseases in auto-immune polyendocrine syndrome type 1].
Proust-Lemoine E, Guyot S. Proust-Lemoine E, et al. Presse Med. 2017 Sep;46(9):853-863. doi: 10.1016/j.lpm.2017.05.029. Epub 2017 Jul 3. Presse Med. 2017. PMID: 28683959 French.
The molecular basis of hereditary enamel defects in humans.
Wright JT, Carrion IA, Morris C. Wright JT, et al. J Dent Res. 2015 Jan;94(1):52-61. doi: 10.1177/0022034514556708. Epub 2014 Nov 11. J Dent Res. 2015. PMID: 25389004 Free PMC article. Review.
SLC13A5 is the second gene associated with Kohlschütter-Tönz syndrome.
Schossig A, Bloch-Zupan A, Lussi A, Wolf NI, Raskin S, Cohen M, Giuliano F, Jurgens J, Krabichler B, Koolen DA, de Macena Sobreira NL, Maurer E, Muller-Bolla M, Penzien J, Zschocke J, Kapferer-Seebacher I. Schossig A, et al. J Med Genet. 2017 Jan;54(1):54-62. doi: 10.1136/jmedgenet-2016-103988. Epub 2016 Sep 6. J Med Genet. 2017. PMID: 27600704 Clinical Trial.
SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects.
Dubail J, Huber C, Chantepie S, Sonntag S, Tüysüz B, Mihci E, Gordon CT, Steichen-Gersdorf E, Amiel J, Nur B, Stolte-Dijkstra I, van Eerde AM, van Gassen KL, Breugem CC, Stegmann A, Lekszas C, Maroofian R, Karimiani EG, Bruneel A, Seta N, Munnich A, Papy-Garcia D, De La Dure-Molla M, Cormier-Daire V. Dubail J, et al. Nat Commun. 2018 Aug 6;9(1):3087. doi: 10.1038/s41467-018-05191-8. Nat Commun. 2018. PMID: 30082715 Free PMC article.
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