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

Year Number of Results
1964 1
1965 1
1966 15
1967 15
1968 12
1969 17
1970 19
1971 32
1972 44
1973 37
1974 49
1975 55
1976 50
1977 59
1978 53
1979 52
1980 51
1981 43
1982 77
1983 83
1984 98
1985 71
1986 87
1987 75
1988 76
1989 106
1990 121
1991 139
1992 149
1993 136
1994 135
1995 131
1996 103
1997 123
1998 149
1999 144
2000 167
2001 186
2002 209
2003 226
2004 216
2005 272
2006 296
2007 313
2008 354
2009 353
2010 443
2011 522
2012 517
2013 579
2014 607
2015 536
2016 571
2017 561
2018 557
2019 394
2020 20
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Article type
Publication date

Search Results

9,531 results
Results by year
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Page 1
Non-invasive pre-implantation genetic diagnosis of X-linked disorders.
Assou S, Aït-Ahmed O, El Messaoudi S, Thierry AR, Hamamah S. Assou S, et al. Med Hypotheses. 2014 Oct;83(4):506-8. doi: 10.1016/j.mehy.2014.08.019. Epub 2014 Aug 23. Med Hypotheses. 2014. PMID: 25182520
A new era in the management of Duchenne muscular dystrophy.
Korinthenberg R. Korinthenberg R. Dev Med Child Neurol. 2019 Mar;61(3):292-297. doi: 10.1111/dmcn.14129. Epub 2018 Dec 16. Dev Med Child Neurol. 2019. PMID: 30556126 Free article. Review.
[Chronic granulomatous disease. Update and review].
López-Hernández I, Suárez-Gutiérrez M, Santos-Chávez EE, Espinosa S, Blancas-Galicia L. López-Hernández I, et al. Rev Alerg Mex. 2019 Apr-Jun;66(2):232-245. doi: 10.29262/ram.v66i2.577. Rev Alerg Mex. 2019. PMID: 31200421 Review. Spanish.
Evidence-Based Consensus and Systematic Review on Reducing the Time to Diagnosis of Duchenne Muscular Dystrophy.
Aartsma-Rus A, Hegde M, Ben-Omran T, Buccella F, Ferlini A, Gallano P, Howell RR, Leturcq F, Martin AS, Potulska-Chromik A, Saute JA, Schmidt WM, Sejersen T, Tuffery-Giraud S, Uyguner ZO, Witcomb LA, Yau S, Nelson SF. Aartsma-Rus A, et al. J Pediatr. 2019 Jan;204:305-313.e14. doi: 10.1016/j.jpeds.2018.10.043. J Pediatr. 2019. PMID: 30579468 Free article. No abstract available.
Case report: a rare case of Hunter syndrome (type II mucopolysaccharidosis) in a girl.
Semyachkina AN, Voskoboeva EY, Zakharova EY, Nikolaeva EA, Kanivets IV, Kolotii AD, Baydakova GV, Kharabadze MN, Kuramagomedova RG, Melnikova NV. Semyachkina AN, et al. BMC Med Genet. 2019 May 2;20(1):66. doi: 10.1186/s12881-019-0807-x. BMC Med Genet. 2019. PMID: 31046699 Free PMC article.
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