Multimodal imaging of striatal degeneration in Amish patients with glutaryl-CoA dehydrogenase deficiency.
about
Genetic mapping of glutaric aciduria, type 3, to chromosome 7 and identification of mutations in c7orf10Neurological Disorders Associated with Striatal Lesions: Classification and Diagnostic Approach.Extrastriatal changes in patients with late-onset glutaric aciduria type I highlight the risk of long-term neurotoxicity.Glutaric acid-mediated apoptosis in primary striatal neuronsIncreased blood-brain barrier permeability and alterations in perivascular astrocytes and pericytes induced by intracisternal glutaric acid.Sensory and motor deficits in children with cerebral palsy born preterm correlate with diffusion tensor imaging abnormalities in thalamocortical pathways.Cerebral haemodynamics in patients with glutaryl-coenzyme A dehydrogenase deficiency.Diagnosis and management of glutaric aciduria type I--revised recommendations.Astrocyte Dysfunction in Developmental Neurometabolic Diseases.N-acetylcysteine prevents spatial memory impairment induced by chronic early postnatal glutaric acid and lipopolysaccharide in rat pups.Leigh syndrome: neuropathology and pathogenesis.Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision.Microarray genomic profile of mitochondrial and oxidant response in manganese chloride treated PC12 cells.Cognitive, behavioural and adaptive profiles of children with glutaric aciduria type I detected through newborn screening.Glutaric Acidemia Type 1: A Case of Infantile Stroke.The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype.Mechanism of metabolic stroke and spontaneous cerebral hemorrhage in glutaric aciduria type I.White matter injury induced by perinatal exposure to glutaric acid.Striatal necrosis in type 1 glutaric aciduria: Different stages in two siblingsLow lysine diet in glutaric aciduria type I--effect on anthropometric and biochemical follow-up parameters.Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I.Induction of Neuroinflammatory Response and Histopathological Alterations Caused by Quinolinic Acid Administration in the Striatum of Glutaryl-CoA Dehydrogenase Deficient Mice.Impairment of astrocytic glutaminolysis in glutaric aciduria type I.Modulatory Effects of Dietary Amino Acids on Neurodegenerative Diseases.Glutaric aciduria type 1: neuroimaging features with clinical correlation.The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation.Unravelling the complex MRI pattern in glutaric aciduria type I using statistical models-a cohort study in 180 patients.Impact of age at onset and newborn screening on outcome in organic acidurias.A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1.Cerebral Organic Acid Disorders and Other Disorders of Lysine Catabolism
P2860
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P2860
Multimodal imaging of striatal degeneration in Amish patients with glutaryl-CoA dehydrogenase deficiency.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh
2007年學術文章
@zh-hant
name
Multimodal imaging of striatal ...... -CoA dehydrogenase deficiency.
@en
Multimodal imaging of striatal ...... -CoA dehydrogenase deficiency.
@nl
type
label
Multimodal imaging of striatal ...... -CoA dehydrogenase deficiency.
@en
Multimodal imaging of striatal ...... -CoA dehydrogenase deficiency.
@nl
prefLabel
Multimodal imaging of striatal ...... -CoA dehydrogenase deficiency.
@en
Multimodal imaging of striatal ...... -CoA dehydrogenase deficiency.
@nl
P2093
P2860
P921
P356
P1433
P1476
Multimodal imaging of striatal ...... -CoA dehydrogenase deficiency.
@en
P2093
D Holmes Morton
Jelena Lazovic
Kevin A Strauss
P2860
P304
P356
10.1093/BRAIN/AWM058
P407
P577
2007-05-03T00:00:00Z