Literature DB >> 25036075

Methylmalonic acidemia with homocystinuria. A very rare cause of kidney failure in the neonatal period.

Orlando Mesa-Medina, Mónica Ruiz-Pons, Víctor García-Nieto, José León-González, Santiago López-Mendoza, Carlos Solís-Reyes.   

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Year:  2014        PMID： 25036075     DOI： 10.3265/Nefrologia.pre2014.May.12058

Source DB:  PubMed          Journal:  Nefrologia        ISSN： 0211-6995            Impact factor:   2.033


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  3 in total

1.  Clinical characteristics of hemolytic uremic syndrome secondary to cobalamin C disorder in Chinese children.

Authors:  Qi-Liang Li; Wen-Qi Song; Xiao-Xia Peng; Xiao-Rong Liu; Le-Jian He; Li-Bing Fu
Journal:  World J Pediatr       Date:  2015-08-08       Impact factor: 2.764

2.  Insights into the molecular mechanisms of methylmalonic acidemia using microarray technology.

Authors:  Lianshu Han; Shengnan Wu; Feng Han; Xuefan Gu
Journal:  Int J Clin Exp Med       Date:  2015-06-15

3.  TAT-MTS-MCM fusion proteins reduce MMA levels and improve mitochondrial activity and liver function in MCM-deficient cells.

Authors:  Tal Erlich-Hadad; Rita Hadad; Anat Feldman; Hagar Greif; Michal Lictenstein; Haya Lorberboum-Galski
Journal:  J Cell Mol Med       Date:  2017-12-19       Impact factor: 5.310
  3 in total

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