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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 16
1994 11
1995 6
1996 6
1997 11
1998 10
1999 9
2000 11
2001 7
2002 7
2003 10
2004 14
2005 10
2006 12
2007 13
2008 9
2009 13
2010 12
2011 12
2012 9
2013 14
2014 9
2015 8
2016 11
2017 15
2018 10
2019 15
2020 23
2021 15
2022 4
2023 9
2024 9
2025 0

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375 results

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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.
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.
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.
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.
Consensus guidelines for the diagnosis and management of succinic semialdehyde dehydrogenase deficiency.
Tokatly Latzer I, Bertoldi M, Blau N, DiBacco ML, Elsea SH, García-Cazorla À, Gibson KM, Gropman AL, Hanson E, Hoffman C, Jeltsch K, Juliá-Palacios N, Knerr I, Lee HHC, Malaspina P, McConnell A, Opladen T, Oppebøen M, Rotenberg A, Walterfang M, Wang-Tso L, Wevers RA, Roullet JB, Pearl PL. Tokatly Latzer I, et al. Among authors: gibson km. Mol Genet Metab. 2024 May;142(1):108363. doi: 10.1016/j.ymgme.2024.108363. Epub 2024 Mar 4. Mol Genet Metab. 2024. PMID: 38452608
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.
Reduced evoked cortical beta and gamma activity and neuronal synchronization in succinic semialdehyde dehydrogenase deficiency, a disorder of γ-aminobutyric acid metabolism.
Papadelis C, Ntolkeras G, Tokatly Latzer I, DiBacco ML, Afacan O, Warfield S, Shi X, Roullet JB, Gibson KM; SSADH Deficiency Investigators Consortium; Pearl PL. Papadelis C, et al. Among authors: gibson km. Brain Commun. 2023 Oct 25;5(6):fcad291. doi: 10.1093/braincomms/fcad291. eCollection 2023. Brain Commun. 2023. PMID: 37953848 Free PMC article.
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder.
Tokatly Latzer I, Roullet JB, Afshar-Saber W, Lee HHC, Bertoldi M, McGinty GE, DiBacco ML, Arning E, Tsuboyama M, Rotenberg A, Opladen T, Jeltsch K, García-Cazorla À, Juliá-Palacios N, Gibson KM, Sahin M, Pearl PL. Tokatly Latzer I, et al. Among authors: gibson km. J Neurodev Disord. 2024 Apr 24;16(1):21. doi: 10.1186/s11689-024-09538-9. J Neurodev Disord. 2024. PMID: 38658850 Free PMC article.
375 results