Author:
Biancheri Roberta,Cerone Roberto,Rossi Andrea,Schiaffino Maria Cristina,Caruso Ubaldo,Minniti Giuseppe,Perrone Maria Viviana,Tortori-Donati Paolo,Veneselli Edvige
Subject
Neurology (clinical),Neurology
Reference23 articles.
1. Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria.;Baumgartner;Helv Paediatr Acta,1979
2. Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC).;Rosenblatt;J Inherit Metab Dis,1997
3. Remethylation defects: guidelines for clinical diagnosis and treatment.;Ogier de Baulny;Eur J Pediatr,1998
4. Genetic defects of folate and cobalamin metabolism.;Fowler;Eur J Pediatr,1998
5. Cobalamin C defect associated with hemolytic-uremic syndrome.;Geraghty;J Pediatr,1992
Cited by
29 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献