Symmetric hypoplasia of the temporal cerebral lobes in an infant with glutaric aciduria type II (multiple acyl-coenzyme A dehydrogenase deficiency).

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Symmetric hypoplasia of the temporal cerebral lobes in an infant with glutaric aciduria type II (multiple acyl-coenzyme A dehydrogenase deficiency). is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/S0022-3476(05)83142-7
P698PubMed publication ID8151478

P2093author name stringRadner H
Ebner F
Hauer A
Stöckler S
Karpf EF
P2860cites workGlutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathyQ38639290
Glutaric aciduria type I: clinical heterogeneity and neuroradiologic featuresQ48198554
Glutaric aciduria: biochemical and morphologic considerationsQ48295638
Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesisQ48900127
Glutaric acidemia type II: clinical, biochemical, and morphologic considerationsQ70375661
P433issue4
P407language of work or nameEnglishQ1860
P921main subjectGlutaric aciduriaQ5572455
P304page(s)601-604
P577publication date1994-04-01
P1433published inThe Journal of PediatricsQ7743611
P1476titleSymmetric hypoplasia of the temporal cerebral lobes in an infant with glutaric aciduria type II (multiple acyl-coenzyme A dehydrogenase deficiency).
P478volume124

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cites work (P2860)
Q37468328Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD).
Q48713528Pathology of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation
Q74662226Proton NMR spectroscopic analysis of multiple acyl-CoA dehydrogenase deficiency--capacity of the choline oxidation pathway for methylation in vivo