The neuropathology of phenylketonuria: human and animal studies.
about
Recent advances in the pathogenesis of syndromic autismsAutism and Metabolic DiseasesPhenylketonuria Pathophysiology: on the Role of Metabolic AlterationsRett syndrome: a prototypical neurodevelopmental disorderA murine model for human sepiapterin-reductase deficiencyThe Fas/Fas ligand death receptor pathway contributes to phenylalanine-induced apoptosis in cortical neuronsDifferential effects of phenylalanine on Rac1, Cdc42, and RhoA expression and activity in cultured cortical neurons5-Hydroxytryptophan during critical postnatal period improves cognitive performances and promotes dendritic spine maturation in genetic mouse model of phenylketonuria.Are neuropsychological impairments in children with early-treated phenylketonuria (PKU) related to white matter abnormalities or elevated phenylalanine levels?Molecular and comparative genetics of mental retardation.PKU is a reversible neurodegenerative process within the nigrostriatum that begins as early as 4 weeks of age in Pah(enu2) miceBreast-feeding success among infants with phenylketonuria.Doxycycline hinders phenylalanine fibril assemblies revealing a potential novel therapeutic approach in phenylketonuriaUnusual presentation of two Chinese phenylketonuria sisters who were misdiagnosed for years.Systematic Review and Meta-Analysis of Neuropsychiatric Symptoms and Executive Functioning in Adults With Phenylketonuria.Dystrophic serotonin axons in postmortem brains from young autism patients.Leukodystrophies: a proposed classification system based on pathological changes and pathogenetic mechanisms.Evidence of Oxidative Stress and Secondary Mitochondrial Dysfunction in Metabolic and Non-Metabolic Disorders.Oligodendrocyte development and myelinogenesis are not impaired by high concentrations of phenylalanine or its metabolites.DNA damage induced by phenylalanine and its analogue p-chlorophenylalanine in blood and brain of rats subjected to a model of hyperphenylalaninemia.Autism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects.AMP-activated protein kinase activation in mediating phenylalanine-induced neurotoxicity in experimental models of phenylketonuria.Phenylalanine reduces synaptic density in mixed cortical cultures from mice.A neuropsychological profile of off-diet adults with phenylketonuria.
P2860
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P2860
The neuropathology of phenylketonuria: human and animal studies.
description
2000 nî lūn-bûn
@nan
2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
The neuropathology of phenylketonuria: human and animal studies.
@ast
The neuropathology of phenylketonuria: human and animal studies.
@en
type
label
The neuropathology of phenylketonuria: human and animal studies.
@ast
The neuropathology of phenylketonuria: human and animal studies.
@en
prefLabel
The neuropathology of phenylketonuria: human and animal studies.
@ast
The neuropathology of phenylketonuria: human and animal studies.
@en
P356
P1476
The neuropathology of phenylketonuria: human and animal studies.
@en
P2093
P R Huttenlocher
P2888
P304
P356
10.1007/PL00014371
P478
159 Suppl 2
P577
2000-10-01T00:00:00Z
P6179
1035380864