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

Year Number of Results
1960 1
1962 1
1963 1
1968 1
1970 1
1971 1
1973 2
1978 3
1980 1
1981 3
1982 3
1983 4
1984 2
1986 1
1987 3
1988 3
1989 7
1990 1
1991 3
1992 4
1993 1
1994 3
1995 3
1996 5
1997 5
1998 2
1999 3
2000 2
2001 2
2002 4
2003 4
2004 6
2005 6
2006 6
2007 3
2008 6
2009 4
2010 7
2011 2
2012 8
2013 8
2014 7
2015 12
2016 4
2017 4
2018 6
2019 2
2021 2
2022 1
2023 1
2024 0

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163 results

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Page 1
A longitudinal study of urea cycle disorders.
Batshaw ML, Tuchman M, Summar M, Seminara J; Members of the Urea Cycle Disorders Consortium. Batshaw ML, et al. Mol Genet Metab. 2014 Sep-Oct;113(1-2):127-30. doi: 10.1016/j.ymgme.2014.08.001. Epub 2014 Aug 10. Mol Genet Metab. 2014. PMID: 25135652 Free PMC article. Review.
Genetic defects in human pyruvate dehydrogenase.
Ho L, Wexler ID, Kerr DS, Patel MS. Ho L, et al. Among authors: kerr ds. Ann N Y Acad Sci. 1989;573:347-59. doi: 10.1111/j.1749-6632.1989.tb15010.x. Ann N Y Acad Sci. 1989. PMID: 2517464 Review.
Participation of CaMKII in neuronal plasticity and memory formation.
Cammarota M, Bevilaqua LR, Viola H, Kerr DS, Reichmann B, Teixeira V, Bulla M, Izquierdo I, Medina JH. Cammarota M, et al. Among authors: kerr ds. Cell Mol Neurobiol. 2002 Jun;22(3):259-67. doi: 10.1023/a:1020763716886. Cell Mol Neurobiol. 2002. PMID: 12469869 Review.
Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium.
Seminara J, Tuchman M, Krivitzky L, Krischer J, Lee HS, Lemons C, Baumgartner M, Cederbaum S, Diaz GA, Feigenbaum A, Gallagher RC, Harding CO, Kerr DS, Lanpher B, Lee B, Lichter-Konecki U, McCandless SE, Merritt JL, Oster-Granite ML, Seashore MR, Stricker T, Summar M, Waisbren S, Yudkoff M, Batshaw ML. Seminara J, et al. Among authors: kerr ds. Mol Genet Metab. 2010;100 Suppl 1(Suppl 1):S97-105. doi: 10.1016/j.ymgme.2010.01.014. Epub 2010 Feb 10. Mol Genet Metab. 2010. PMID: 20188616 Free PMC article. Review.
163 results