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For: Chen M, Zhuang J, Yang J, Wang D, Yang Q. Atypical hemolytic uremic syndrome induced by CblC subtype of methylmalonic academia: A case report and literature review. Medicine (Baltimore) 2017;96:e8284. [PMID: 29068997 DOI: 10.1097/MD.0000000000008284] [Cited by in Crossref: 10] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Juan T, Chao-ying C, Hua-rong L, Ling W. Rare cause of coronary artery ectasia in children: A case report of methylmalonic acidemia with hyperhomocysteinemia. Front Pediatr 2022;10:917734. [DOI: 10.3389/fped.2022.917734] [Reference Citation Analysis]
2 Wasim M, Khan HN, Ayesha H, Awan FR. Biochemical screening of intellectually disabled and healthy children in Punjab, Pakistan: differences in liver function test and lipid profiles. Int J Dev Disabil 2019;66:190-5. [PMID: 34141381 DOI: 10.1080/20473869.2018.1533084] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
3 Wang Y, Sun Y, Jiang T. Clinical Application of LC-MS/MS in the Follow-Up for Treatment of Children with Methylmalonic Aciduria. Adv Ther 2019;36:1304-13. [PMID: 31049874 DOI: 10.1007/s12325-019-00955-0] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 3.3] [Reference Citation Analysis]
4 Chen RY, Li XZ, Lin Q, Zhu Y, Shen YY, Xu QY, Zhu XM, Chen LQ, Wu HY, Chen XQ. Proteinuria as a presenting sign of combined methylmalonic acidemia and homocysteinemia: case report. BMC Med Genet 2020;21:183. [PMID: 32957924 DOI: 10.1186/s12881-020-01122-x] [Reference Citation Analysis]
5 Wang Q, Wang Q, Gao Y, Tang C, Gao Z, Hu Z. Case Report: Membranous Nephropathy Secondary to Cobalamin C Disease. Front Med 2022;8:807017. [DOI: 10.3389/fmed.2021.807017] [Reference Citation Analysis]
6 Wiedemann A, Oussalah A, Lamireau N, Théron M, Julien M, Mergnac JP, Augay B, Deniaud P, Alix T, Frayssinoux M, Feillet F, Guéant JL. Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B12 metabolism: A meta-analysis. Cell Rep Med 2022;:100670. [PMID: 35764087 DOI: 10.1016/j.xcrm.2022.100670] [Reference Citation Analysis]
7 Hu S, Mei S, Liu N, Kong X. Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and homocystinuria. BMC Med Genet 2018;19:154. [PMID: 30157807 DOI: 10.1186/s12881-018-0666-x] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]