scholarly article | Q13442814 |
P356 | DOI | 10.1017/S0317167100007836 |
P698 | PubMed publication ID | 19650361 |
P2093 | author name string | Chandrakant Rao | |
Miguel Guzman | |||
Virginia Anderson | |||
Xianyuan Song | |||
P2860 | cites work | A severely brain-damaged case of 3-hydroxyisobutyric aciduria | Q34263898 |
Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation | Q34574663 | ||
Neuropathological, biochemical and molecular findings in a glutaric acidemia type 1 cohort | Q42473849 | ||
3-Hydroxyisobutyric aciduria: an inborn error of valine metabolism | Q46049286 | ||
Evidence that 3-hydroxyisobutyric acid inhibits key enzymes of energy metabolism in cerebral cortex of young rats | Q46711572 | ||
Basal ganglia lesions in a patient with 3-hydroxyisobutyric aciduria | Q48531174 | ||
Septo-optic dysplasia with cerebellar hypoplasia in Cornelia de Lange syndrome | Q48851956 | ||
3-hydroxyisobutyric aciduria with a mild clinical course | Q71755026 | ||
3-Hydroxyisobutyric aciduria in two brothers | Q74502569 | ||
Clinical, biochemical, and molecular findings in three patients with 3-hydroxyisobutyric aciduria | Q24304109 | ||
Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduria | Q28320742 | ||
Dysmyelination in the brain of adolescents and young adults with maple syrup urine disease | Q30925488 | ||
3-Hydroxyisobutyric aciduria: phenotypic heterogeneity within a single family | Q34083564 | ||
P433 | issue | 4 | |
P921 | main subject | autopsy | Q41482 |
P304 | page(s) | 483-486 | |
P577 | publication date | 2009-07-01 | |
P1433 | published in | Canadian Journal of Neurological Sciences | Q5030246 |
P1476 | title | Neuropathology of 3-hydroxyisobutyric aciduria, an autopsy case report | |
P478 | volume | 36 |