These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
189 related articles for article (PubMed ID: 26268900)
1. Natural history of succinic semialdehyde dehydrogenase deficiency through adulthood. Lapalme-Remis S; Lewis EC; De Meulemeester C; Chakraborty P; Gibson KM; Torres C; Guberman A; Salomons GS; Jakobs C; Ali-Ridha A; Parviz M; Pearl PL Neurology; 2015 Sep; 85(10):861-5. PubMed ID: 26268900 [TBL] [Abstract][Full Text] [Related]
2. SSADH deficiency in an adult: Venturing outside of the diagnostic box and inside of the registry. Bertini E; Gospe SM Neurology; 2015 Sep; 85(10):842-3. PubMed ID: 26268899 [No Abstract] [Full Text] [Related]
3. Age-related phenotype and biomarker changes in SSADH deficiency. DiBacco ML; Roullet JB; Kapur K; Brown MN; Walters DC; Gibson KM; Pearl PL Ann Clin Transl Neurol; 2019 Jan; 6(1):114-120. PubMed ID: 30656189 [TBL] [Abstract][Full Text] [Related]
4. Succinic Semialdehyde Dehydrogenase Deficiency: Review of the Natural History Study. Pearl PL; DiBacco ML; Papadelis C; Opladen T; Hanson E; Roullet JB; Gibson KM J Child Neurol; 2021 Nov; 36(13-14):1153-1161. PubMed ID: 33393837 [TBL] [Abstract][Full Text] [Related]
12. Succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetuses. Li X; Ding Y; Liu Y; Zhang Y; Song J; Wang Q; Li M; Qin Y; Huang S; Yang Y Gene; 2015 Dec; 574(1):41-7. PubMed ID: 26220405 [TBL] [Abstract][Full Text] [Related]
13. Clinical diagnosis and mutation analysis of four Chinese families with succinic semialdehyde dehydrogenase deficiency. Wang P; Cai F; Cao L; Wang Y; Zou Q; Zhao P; Wang C; Zhang Y; Cai C; Shu J BMC Med Genet; 2019 May; 20(1):88. PubMed ID: 31117962 [TBL] [Abstract][Full Text] [Related]
14. Magnetic Resonance Imaging (MRI) and Spectroscopy in Succinic Semialdehyde Dehydrogenase Deficiency. Afacan O; Yang E; Lin AP; Coello E; DiBacco ML; Pearl PL; Warfield SK; Consortium SDI J Child Neurol; 2021 Nov; 36(13-14):1162-1168. PubMed ID: 33557675 [TBL] [Abstract][Full Text] [Related]
15. 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 J Perinat Med; 2016 May; 44(4):441-51. PubMed ID: 25431891 [TBL] [Abstract][Full Text] [Related]
16. Pathophysiology and management of neuropsychiatric symptoms in succinic semialdehyde dehydrogenase deficiency. Phakey S; Walterfang M Psychiatr Genet; 2021 Jun; 31(3):100-101. PubMed ID: 33953124 [No Abstract] [Full Text] [Related]
17. A boy with a severe phenotype of succinic semialdehyde dehydrogenase deficiency. Yamakawa Y; Nakazawa T; Ishida A; Saito N; Komatsu M; Matsubara T; Obinata K; Hirose S; Okumura A; Shimizu T Brain Dev; 2012 Feb; 34(2):107-12. PubMed ID: 21612881 [TBL] [Abstract][Full Text] [Related]