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

Year Number of Results
1982 2
1983 2
1984 6
1985 3
1986 5
1987 1
1988 10
1989 7
1990 6
1991 4
1992 9
1993 17
1994 11
1995 6
1996 6
1997 11
1998 10
1999 9
2000 11
2001 7
2002 7
2003 10
2004 15
2005 10
2006 12
2007 13
2008 9
2009 13
2010 12
2011 12
2012 9
2013 14
2014 9
2015 8
2016 12
2017 14
2018 10
2019 15
2020 22
2021 15
2022 1
Text availability
Article attribute
Article type
Publication date

Search Results

355 results
Results by year
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Page 1
Gamma-hydroxybutyric acid.
Snead OC 3rd, Gibson KM. Snead OC 3rd, et al. Among authors: gibson km. N Engl J Med. 2005 Jun 30;352(26):2721-32. doi: 10.1056/NEJMra044047. N Engl J Med. 2005. PMID: 15987921 Review. No abstract available.
Succinic Semialdehyde Dehydrogenase Deficiency.
Pearl PL, Wiwattanadittakul N, Roullet JB, Gibson KM. Pearl PL, et al. Among authors: gibson km. 2004 May 5 [updated 2016 Apr 28]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2004 May 5 [updated 2016 Apr 28]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301374 Free Books & Documents. Review.
Phenotype of GABA-transaminase deficiency.
Koenig MK, Hodgeman R, Riviello JJ, Chung W, Bain J, Chiriboga CA, Ichikawa K, Osaka H, Tsuji M, Gibson KM, Bonnen PE, Pearl PL. Koenig MK, et al. Among authors: gibson km. Neurology. 2017 May 16;88(20):1919-1924. doi: 10.1212/WNL.0000000000003936. Epub 2017 Apr 14. Neurology. 2017. PMID: 28411234 Free PMC article. Review.
Pediatric neurotransmitter diseases.
Pearl PL, Wallis DD, Gibson KM. Pearl PL, et al. Among authors: gibson km. Curr Neurol Neurosci Rep. 2004 Mar;4(2):147-52. doi: 10.1007/s11910-004-0029-1. Curr Neurol Neurosci Rep. 2004. PMID: 14984687 Review.
Clinical Use of CSF Neurotransmitters.
Rodan LH, Gibson KM, Pearl PL. Rodan LH, et al. Among authors: gibson km. Pediatr Neurol. 2015 Oct;53(4):277-86. doi: 10.1016/j.pediatrneurol.2015.04.016. Epub 2015 Jun 11. Pediatr Neurol. 2015. PMID: 26194033 Review.
Therapeutic liver repopulation for phenylketonuria.
Harding CO, Gibson KM. Harding CO, et al. Among authors: gibson km. J Inherit Metab Dis. 2010 Dec;33(6):681-7. doi: 10.1007/s10545-010-9099-1. Epub 2010 May 22. J Inherit Metab Dis. 2010. PMID: 20495959 Review.
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: gibson km. J Inherit Metab Dis. 1999 Jun;22(4):414-27. doi: 10.1023/a:1005500122231. J Inherit Metab Dis. 1999. PMID: 10407778 Review.
Proceedings of the International SSADH Deficiency 2020 Conference.
Pearl PL, DiBacco ML, Roullet JB, Gibson KM. Pearl PL, et al. Among authors: gibson km. J Child Neurol. 2021 Nov;36(13-14):1151-1152. doi: 10.1177/08830738211061930. Epub 2021 Nov 20. J Child Neurol. 2021. PMID: 34806467 No abstract available.
355 results