Literature DB >> 5726767

Development of myelin in inherited disorders of amino acid metabolism.

A L Prensky, S Carr, H W Moser.   

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Year:  1968        PMID: 5726767     DOI: 10.1001/archneur.1968.00480060022002

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


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  8 in total

1.  Maple syrup urine disease (branched chain ketoaciduria).

Authors:  P A Harper; P J Healy; J A Dennis
Journal:  Am J Pathol       Date:  1990-06       Impact factor: 4.307

2.  Mental retardation and the biochemistry of the developing brain.

Authors:  A N Davison
Journal:  Proc R Soc Med       Date:  1972-07

3.  Cerebral ribosomal protein phosphorylation in experimental hyperphenylalaninaemia.

Authors:  S Roberts; B S Morelos
Journal:  Biochem J       Date:  1980-08-15       Impact factor: 3.857

4.  Neurological deterioration in adult phenylketonuria.

Authors:  D Villasana; I J Butler; J C Williams; S M Roongta
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

5.  Infantile spongy degeneration of the central nervous system associated with glycogen storage and markedly fatty liver.

Authors:  Y Takei; G B Solitare
Journal:  J Neurol Neurosurg Psychiatry       Date:  1972-02       Impact factor: 10.154

6.  Myelination in the developing human brain: biochemical correlates.

Authors:  H C Kinney; J Karthigasan; N I Borenshteyn; J D Flax; D A Kirschner
Journal:  Neurochem Res       Date:  1994-08       Impact factor: 3.996

7.  Inhibition by the branched-chain 2-oxo acids of the 2-oxoglutarate dehydrogenase complex in developing rat and human brain.

Authors:  M S Patel
Journal:  Biochem J       Date:  1974-10       Impact factor: 3.857

8.  An occipito-temporal syndrome in adolescents with optimally controlled hyperphenylalaninaemia.

Authors:  H C Lou; P B Toft; J Andresen; I Mikkelsen; B Olsen; F Güttler; S Wieslander; O Henriksen
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

  8 in total

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