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6. Clinical aspects of the disorders of GABA metabolism in children. Pearl PL; Gibson KM Curr Opin Neurol; 2004 Apr; 17(2):107-13. PubMed ID: 15021235 [TBL] [Abstract][Full Text] [Related]
7. The pediatric neurotransmitter disorders. Pearl PL; Taylor JL; Trzcinski S; Sokohl A J Child Neurol; 2007 May; 22(5):606-16. PubMed ID: 17690069 [TBL] [Abstract][Full Text] [Related]
8. Disorders of amino acid metabolism associated with epilepsy. Lee WT Brain Dev; 2011 Oct; 33(9):745-52. PubMed ID: 21803516 [TBL] [Abstract][Full Text] [Related]
9. Metabolism of amino acid neurotransmitters: the synaptic disorder underlying inherited metabolic diseases. Kölker S J Inherit Metab Dis; 2018 Nov; 41(6):1055-1063. PubMed ID: 29869166 [TBL] [Abstract][Full Text] [Related]
10. Murine succinate semialdehyde dehydrogenase (SSADH) deficiency, a heritable disorder of GABA metabolism with epileptic phenotype. Gibson KM; Jakobs C; Pearl PL; Snead OC IUBMB Life; 2005 Sep; 57(9):639-44. PubMed ID: 16203683 [TBL] [Abstract][Full Text] [Related]
11. Variations of dopamine, serotonin, and amino acid concentrations in Noda epileptic rat (NER) retina. Chanut E; Labarthe B; Lacroix B; Noda A; Gasdeblay S; Bondier JR; Versaux-Botteri C Brain Res; 2006 Jan; 1070(1):56-64. PubMed ID: 16403472 [TBL] [Abstract][Full Text] [Related]
12. Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency. Dervent A; Gibson KM; Pearl PL; Salomons GS; Jakobs C; Yalcinkaya C Clin Neurophysiol; 2004 Jun; 115(6):1417-22. PubMed ID: 15134710 [TBL] [Abstract][Full Text] [Related]
13. Glycine metabolism and spinal cord disorders. Bank WJ; Pizer L; Pfendner W Adv Neurol; 1978; 21():267-78. PubMed ID: 216244 [No Abstract] [Full Text] [Related]
14. Review: Normal and abnormal central nervous system GABA metabolism in childhood. Jaeken J; Casaer P; Haegele KD; Schechter PJ J Inherit Metab Dis; 1990; 13(6):793-801. PubMed ID: 2079831 [TBL] [Abstract][Full Text] [Related]
15. 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 Neurochem Int; 2016 Oct; 99():72-84. PubMed ID: 27311541 [TBL] [Abstract][Full Text] [Related]
16. [Gamma-aminobutyric acid--metabolism and its disorders]. Kowalski A; Rebas E; Zylińska L Postepy Biochem; 2007; 53(4):356-60. PubMed ID: 19024900 [TBL] [Abstract][Full Text] [Related]
20. Inborn Errors of Metabolism with Seizures: Defects of Glycine and Serine Metabolism and Cofactor-Related Disorders. Almannai M; El-Hattab AW Pediatr Clin North Am; 2018 Apr; 65(2):279-299. PubMed ID: 29502914 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]