Liver transplantation is not curative for methylmalonic acidopathy caused by methylmalonyl-CoA mutase deficiency
about
Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemiaA detailed analysis of methylmalonic acid kinetics during hemodialysis and after combined liver/kidney transplantation in a patient with mut (0) methylmalonic acidemiaLiver-directed recombinant adeno-associated viral gene delivery rescues a lethal mouse model of methylmalonic acidemia and provides long-term phenotypic correctionAdenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytesMetabolic phenotype of methylmalonic acidemia in mice and humans: the role of skeletal muscleLong-term rescue of a lethal murine model of methylmalonic acidemia using adeno-associated viral gene therapy.Correction of methylmalonic aciduria in vivo using a codon-optimized lentiviral vector.Gene therapy in a murine model of methylmalonic acidemia using rAAV9-mediated gene deliveryBrain damage in methylmalonic aciduria: 2-methylcitrate induces cerebral ammonium accumulation and apoptosis in 3D organotypic brain cell cultures.The proteome of methylmalonic acidemia (MMA): the elucidation of altered pathways in patient liversCombined liver-kidney transplant for the management of methylmalonic aciduria: a case report and review of the literatureMitochondrial dysfunction in mut methylmalonic acidemia.Adenovirus-mediated gene delivery rescues a neonatal lethal murine model of mut(0) methylmalonic acidemia.Successful Domino Liver Transplantation from a Patient with Methylmalonic Acidemia.Renal dysfunction in methylmalonic acidurias: review for the pediatric nephrologist.2-Methylcitric acid impairs glutamate metabolism and induces permeability transition in brain mitochondria.Experimental evidence that methylmalonic acid provokes oxidative damage and compromises antioxidant defenses in nerve terminal and striatum of young rats.Improvement in the prognosis and development of patients with methylmalonic acidemia after living donor liver transplant.Impaired Health-Related Quality of Life in Children and Families Affected by Methylmalonic Acidemia.The syndrome of deafness-dystonia: clinical and genetic heterogeneity.Disorders of branched chain amino acid metabolism.
P2860
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P2860
Liver transplantation is not curative for methylmalonic acidopathy caused by methylmalonyl-CoA mutase deficiency
description
2006 nî lūn-bûn
@nan
2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@ast
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@en
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@nl
type
label
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@ast
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@en
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@nl
prefLabel
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@ast
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@en
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@nl
P2093
P1476
Liver transplantation is not c ...... lmalonyl-CoA mutase deficiency
@en
P2093
Alice T Mazur
Michael J Palmieri
Paige Kaplan
P356
10.1016/J.YMGME.2006.04.003
P407
P577
2006-08-01T00:00:00Z