Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approach.
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Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemiaCandidate genes in quantitative trait loci associated with absolute and relative kidney weight in rats with Inherited Stress Induced Arterial Hypertension.Maleic Acid--but Not Structurally Related Methylmalonic Acid--Interrupts Energy Metabolism by Impaired Calcium Homeostasis.Neurocognitive phenotype of isolated methylmalonic acidemiaPopulation prevalence, attributable risk, and attributable risk percentage for high methylmalonic acid concentrations in the post-folic acid fortification period in the US.Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency.Candida albicans utilizes a modified β-oxidation pathway for the degradation of toxic propionyl-CoA.Mitochondrial energy metabolism in neurodegeneration associated with methylmalonic acidemia.Renal dysfunction in methylmalonic acidurias: review for the pediatric nephrologist.Current concepts in organic acidurias: understanding intra- and extracerebral disease manifestation.Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduria.Novel Mouse Models of Methylmalonic Aciduria Recapitulate Phenotypic Traits with a Genetic Dosage Effect.The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype.Increased susceptibility of brain acetylcholinesterase activity to methylmalonate in young rats with renal failure.Atypical hemolytic uremic syndrome induced by CblC subtype of methylmalonic academia: A case report and literature review.A neuronal disruption in redox homeostasis elicited by ammonia alters the glycine/glutamate (GABA) cycle and contributes to MMA-induced excitability.Renal Involvement in Methylmalonic Aciduria.Population Reference Values for Serum Methylmalonic Acid Concentrations and Its Relationship with Age, Sex, Race-Ethnicity, Supplement Use, Kidney Function and Serum Vitamin B12 in the Post-Folic Acid Fortification Period.Acute renal failure potentiates methylmalonate-induced oxidative stress in brain and kidney of rats.Methylmalonate impairs mitochondrial respiration supported by NADH-linked substrates: involvement of mitochondrial glutamate metabolism.Organic acidurias in adults: late complications and management.Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemia.Cobalamin C defect-hemolytic uremic syndrome caused by new mutation in MMACHC.Cognitive and social profiles in two patients with cobalamin C disease.Altered Redox Homeostasis in Branched-Chain Amino Acid Disorders, Organic Acidurias, and Homocystinuria.Disorders of branched chain amino acid metabolism.Disclosure of a putative biosignature for respiratory chain disorders through a metabolomics approach
P2860
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P2860
Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approach.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Neurodegeneration and chronic ...... a pathophysiological approach.
@en
type
label
Neurodegeneration and chronic ...... a pathophysiological approach.
@en
prefLabel
Neurodegeneration and chronic ...... a pathophysiological approach.
@en
P2093
P1476
Neurodegeneration and chronic ...... a pathophysiological approach.
@en
P2093
Hoffmann GF
P2888
P356
10.1007/S10545-007-0571-5
P577
2007-09-12T00:00:00Z