Related Articles by Review for PMID: 32809559

Year	Number of Results
1993	2
1998	1
2003	4
2004	2
2009	1
2011	1
2013	1
2014	1
2015	2
2016	3
2018	1
2019	1
2020	1
2022	1
2023	1
2025	2

1

Succinic Semialdehyde Dehydrogenase Deficiency.

Sergi C, Parayil Sankaran B. Sergi C, et al. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 32809559 Free Books & Documents.

2

Temporal metabolomics in dried bloodspots suggests multipathway disruptions in aldh5a1^-/- mice, a model of succinic semialdehyde dehydrogenase deficiency.

Brown M, Turgeon C, Rinaldo P, Roullet JB, Gibson KM. Brown M, et al. Mol Genet Metab. 2019 Dec;128(4):397-408. doi: 10.1016/j.ymgme.2019.10.003. Epub 2019 Oct 31. Mol Genet Metab. 2019. PMID: 31699650 Review.

3

Succinic Semialdehyde Dehydrogenase Deficiency.

Tokatly Latzer I, Pearl PL, Roullet JB. Tokatly Latzer I, et al. 2004 May 5 [updated 2025 Jan 9]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2004 May 5 [updated 2025 Jan 9]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301374 Free Books & Documents. Review.

4

Understanding the Molecular Mechanisms of Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD): Towards the Development of SSADH-Targeted Medicine.

Lee HHC, McGinty GE, Pearl PL, Rotenberg A. Lee HHC, et al. Int J Mol Sci. 2022 Feb 26;23(5):2606. doi: 10.3390/ijms23052606. Int J Mol Sci. 2022. PMID: 35269750 Free PMC article. Review.

5

Mutation analysis and prenatal diagnosis in a Chinese family with succinic semialdehyde dehydrogenase and a systematic review of the literature of reported ALDH5A1 mutations.

Liu N, Kong XD, Kan QC, Shi HR, Wu QH, Zhuo ZH, Bai QL, Jiang M. Liu N, et al. J Perinat Med. 2016 May 1;44(4):441-51. doi: 10.1515/jpm-2014-0164. J Perinat Med. 2016. PMID: 25431891 Review.

6

Comparative genomics of aldehyde dehydrogenase 5a1 (succinate semialdehyde dehydrogenase) and accumulation of gamma-hydroxybutyrate associated with its deficiency.

Malaspina P, Picklo MJ, Jakobs C, Snead OC, Gibson KM. Malaspina P, et al. Hum Genomics. 2009 Jan;3(2):106-20. doi: 10.1186/1479-7364-3-2-106. Hum Genomics. 2009. PMID: 19164088 Free PMC article. Review.

7

Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolism.

Malaspina P, Roullet JB, Pearl PL, Ainslie GR, Vogel KR, Gibson KM. Malaspina P, et al. Neurochem Int. 2016 Oct;99:72-84. doi: 10.1016/j.neuint.2016.06.009. Epub 2016 Jun 14. Neurochem Int. 2016. PMID: 27311541 Free PMC article. Review.

8

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.

9

Vigabatrin and newer interventions in succinic semialdehyde dehydrogenase deficiency.

Gropman A. Gropman A. Ann Neurol. 2003;54 Suppl 6:S66-72. doi: 10.1002/ana.10626. Ann Neurol. 2003. PMID: 12891656 Review.

10

Succinic semialdehyde dehydrogenase: biochemical-molecular-clinical disease mechanisms, redox regulation, and functional significance.

Kim KJ, Pearl PL, Jensen K, Snead OC, Malaspina P, Jakobs C, Gibson KM. Kim KJ, et al. Antioxid Redox Signal. 2011 Aug 1;15(3):691-718. doi: 10.1089/ars.2010.3470. Epub 2011 Apr 10. Antioxid Redox Signal. 2011. PMID: 20973619 Free PMC article. Review.

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