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For: Finsterer J, Scorza FA, Fiorini AC, Scorza CA. MEGDEL Syndrome. Pediatr Neurol 2020;110:25-9. [PMID: 32684373 DOI: 10.1016/j.pediatrneurol.2020.03.009] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Fellman V, Banerjee R, Lin KL, Pulli I, Cooper H, Tyynismaa H, Kallijärvi J. Severe neonatal MEGDHEL syndrome with a homozygous truncating mutation in SERAC1. Biochim Biophys Acta Mol Basis Dis 2021;1868:166298. [PMID: 34751152 DOI: 10.1016/j.bbadis.2021.166298] [Reference Citation Analysis]
2 Jones DE, Klacking E, Ryan RO. Inborn errors of metabolism associated with 3-methylglutaconic aciduria. Clin Chim Acta 2021;522:96-104. [PMID: 34411555 DOI: 10.1016/j.cca.2021.08.016] [Reference Citation Analysis]
3 Lin CW, Huang CW, Luo AC, Chou YT, Huang YS, Chen PL, Chen TC. Genetic Spectrum and Characteristics of Hereditary Optic Neuropathy in Taiwan. Genes (Basel) 2021;12:1378. [PMID: 34573359 DOI: 10.3390/genes12091378] [Reference Citation Analysis]
4 Yan D, Chen S, Cai F, Shu J, Zhi X, Zheng J, Zhang C, Li D, Cai C. Complicated Hereditary Spastic Paraplegia Caused by SERAC1 Variants in a Chinese Family. Front Pediatr 2022;9:816265. [DOI: 10.3389/fped.2021.816265] [Reference Citation Analysis]
5 Fang H, Xie A, Du M, Li X, Yang K, Fu Y, Yuan X, Fan R, Yu W, Zhou Z, Sang T, Nie K, Li J, Zhao Q, Chen Z, Yang Y, Hong C, Lyu J. SERAC1 is a component of the mitochondrial serine transporter complex required for the maintenance of mitochondrial DNA. Sci Transl Med 2022;14:eabl6992. [PMID: 35235340 DOI: 10.1126/scitranslmed.abl6992] [Reference Citation Analysis]
6 D'Arco F, Mertiri L, de Graaf P, De Foer B, Popovič KS, Argyropoulou MI, Mankad K, Brisse HJ, Juliano A, Severino M, Van Cauter S, Ho ML, Robson CD, Siddiqui A, Connor S, Bisdas S; Consensus for Magnetic Resonance Protocols Study (COMPS) Group. Guidelines for magnetic resonance imaging in pediatric head and neck pathologies: a multicentre international consensus paper. Neuroradiology 2022. [PMID: 35460348 DOI: 10.1007/s00234-022-02950-9] [Reference Citation Analysis]
7 Su Y, Zhang H, Wang H, Wu B, Yang J, Zhou W, Li L. Case Report: Progressive Cholestasis: Severe Phenotype of MEGDEL Syndrome With SATB2-Associated Syndrome. Front Pediatr 2021;9:713458. [PMID: 34660482 DOI: 10.3389/fped.2021.713458] [Reference Citation Analysis]
8 Horvath B, Pfister KM, Rupp A, Kloesel B. MEGDEL Syndrome and Its Anesthetic Implications. Cureus 2021;13:e17761. [PMID: 34540505 DOI: 10.7759/cureus.17761] [Reference Citation Analysis]