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

Year Number of Results
1990 6
1991 12
1992 16
1993 16
1994 10
1995 7
1996 5
1997 11
1998 9
1999 11
2000 6
2001 9
2002 12
2003 7
2004 3
2005 4
2006 5
2007 6
2008 1
2009 6
2010 1
2011 8
2012 4
2013 1
2014 3
2015 2
2016 1
2022 0
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Search Results

177 results
Results by year
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Page 1
Aneurysm syndromes caused by mutations in the TGF-beta receptor.
Loeys BL, Schwarze U, Holm T, Callewaert BL, Thomas GH, Pannu H, De Backer JF, Oswald GL, Symoens S, Manouvrier S, Roberts AE, Faravelli F, Greco MA, Pyeritz RE, Milewicz DM, Coucke PJ, Cameron DE, Braverman AC, Byers PH, De Paepe AM, Dietz HC. Loeys BL, et al. N Engl J Med. 2006 Aug 24;355(8):788-98. doi: 10.1056/NEJMoa055695. N Engl J Med. 2006. PMID: 16928994 Free article.
Adrenoleukodystrophy.
Moser HW, Bergin A, Naidu S, Ladenson PW. Moser HW, et al. Endocrinol Metab Clin North Am. 1991 Jun;20(2):297-318. Endocrinol Metab Clin North Am. 1991. PMID: 1879401 Review.
Peroxisomal disorders.
Moser HW, Bergin A, Cornblath D. Moser HW, et al. Biochem Cell Biol. 1991 Jul;69(7):463-74. doi: 10.1139/o91-070. Biochem Cell Biol. 1991. PMID: 1724376 Review.
Fragile X syndrome.
Reiss AL, Freund L. Reiss AL, et al. Biol Psychiatry. 1990 Jan 15;27(2):223-40. doi: 10.1016/0006-3223(90)90652-i. Biol Psychiatry. 1990. PMID: 2403814 Review.
Neuroimaging studies in Rett syndrome.
Naidu S, Kaufmann WE, Abrams MT, Pearlson GD, Lanham DC, Fredericksen KA, Barker PB, Horska A, Golay X, Mori S, Wong DF, Yablonski M, Moser HW, Johnston MV. Naidu S, et al. Brain Dev. 2001 Dec;23 Suppl 1:S62-71. doi: 10.1016/s0387-7604(01)00381-3. Brain Dev. 2001. PMID: 11738844 Review.
X-linked adrenoleukodystrophy: genes, mutations, and phenotypes.
Smith KD, Kemp S, Braiterman LT, Lu JF, Wei HM, Geraghty M, Stetten G, Bergin JS, Pevsner J, Watkins PA. Smith KD, et al. Neurochem Res. 1999 Apr;24(4):521-35. doi: 10.1023/a:1022535930009. Neurochem Res. 1999. PMID: 10227685 Review.
Advances in the treatment of fragile X syndrome.
Hagerman RJ, Berry-Kravis E, Kaufmann WE, Ono MY, Tartaglia N, Lachiewicz A, Kronk R, Delahunty C, Hessl D, Visootsak J, Picker J, Gane L, Tranfaglia M. Hagerman RJ, et al. Pediatrics. 2009 Jan;123(1):378-90. doi: 10.1542/peds.2008-0317. Pediatrics. 2009. PMID: 19117905 Free PMC article. Review.
Molecular and cellular genetics of fragile X syndrome.
Kaufmann WE, Reiss AL. Kaufmann WE, et al. Am J Med Genet. 1999 Feb 5;88(1):11-24. doi: 10.1002/(sici)1096-8628(19990205)88:1<11::aid-ajmg3>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10050961 Review. No abstract available.
177 results