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

Year Number of Results
1973 1
1977 3
1978 3
1980 2
1981 2
1982 1
1983 2
1984 10
1985 1
1986 1
1987 4
1988 5
1989 8
1990 19
1991 16
1992 15
1993 17
1994 12
1995 16
1996 15
1997 20
1998 37
1999 29
2000 20
2001 17
2002 14
2003 22
2004 26
2005 37
2006 32
2007 29
2008 22
2009 27
2010 32
2011 27
2012 21
2013 18
2014 7
2015 4
2016 2
2017 3
2018 2
2020 1
2022 0
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572 results
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Page 1
Progress in understanding 2-hydroxyglutaric acidurias.
Kranendijk M, Struys EA, Salomons GS, Van der Knaap MS, Jakobs C. Kranendijk M, et al. Among authors: jakobs c. J Inherit Metab Dis. 2012 Jul;35(4):571-87. doi: 10.1007/s10545-012-9462-5. Epub 2012 Mar 6. J Inherit Metab Dis. 2012. PMID: 22391998 Free PMC article. Review.
D-2-hydroxyglutaric aciduria.
Nyhan WL, Shelton GD, Jakobs C, Holmes B, Bowe C, Curry CJ, Vance C, Duran M, Sweetman L. Nyhan WL, et al. Among authors: jakobs c. J Child Neurol. 1995 Mar;10(2):137-42. doi: 10.1177/088307389501000216. J Child Neurol. 1995. PMID: 7782605
4-Aminobutyrate aminotransferase (GABA-transaminase) deficiency.
Medina-Kauwe LK, Tobin AJ, De Meirleir L, Jaeken J, Jakobs C, Nyhan WL, Gibson KM. Medina-Kauwe LK, et al. Among authors: jakobs c. J Inherit Metab Dis. 1999 Jun;22(4):414-27. doi: 10.1023/a:1005500122231. J Inherit Metab Dis. 1999. PMID: 10407778 Review.
Immunoblotting for active caspase-1.
Jakobs C, Bartok E, Kubarenko A, Bauernfeind F, Hornung V. Jakobs C, et al. Methods Mol Biol. 2013;1040:103-15. doi: 10.1007/978-1-62703-523-1_9. Methods Mol Biol. 2013. PMID: 23852600
Multiple syndromes of 3-methylglutaconic aciduria.
Gibson KM, Elpeleg ON, Jakobs C, Costeff H, Kelley RI. Gibson KM, et al. Among authors: jakobs c. Pediatr Neurol. 1993 Mar-Apr;9(2):120-3. doi: 10.1016/0887-8994(93)90046-f. Pediatr Neurol. 1993. PMID: 8499040 Review.
N-acetylaspartylglutamate in CNS hypomyelination.
Wamelink MM, Struys E, Holwerda U, Sistermans EA, van Spaendonk RM, Halley D, Willemsen MA, Jakobs C, van der Knaap MS, Wolf NI. Wamelink MM, et al. Among authors: jakobs c. Neuropediatrics. 2011 Feb;42(2):74-7. doi: 10.1055/s-0031-1277176. Epub 2011 May 3. Neuropediatrics. 2011. PMID: 21544765
Murine succinate semialdehyde dehydrogenase deficiency.
Gupta M, Hogema BM, Grompe M, Bottiglieri TG, Concas A, Biggio G, Sogliano C, Rigamonti AE, Pearl PL, Snead OC 3rd, Jakobs C, Gibson KM. Gupta M, et al. Among authors: jakobs c. Ann Neurol. 2003;54 Suppl 6:S81-90. doi: 10.1002/ana.10625. Ann Neurol. 2003. PMID: 12891658 Review.
Inherited disorders of GABA metabolism.
Jakobs C, Jaeken J, Gibson KM. Jakobs C, et al. J Inherit Metab Dis. 1993;16(4):704-15. doi: 10.1007/BF00711902. J Inherit Metab Dis. 1993. PMID: 8412016 Review.
572 results