Neuropathology of 3-hydroxyisobutyric aciduria, an autopsy case report.

scientific article published in July 2009

Neuropathology of 3-hydroxyisobutyric aciduria, an autopsy case report. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1017/S0317167100007836
P698PubMed publication ID19650361

P2093author name stringChandrakant Rao
Miguel Guzman
Virginia Anderson
Xianyuan Song
P2860cites workA severely brain-damaged case of 3-hydroxyisobutyric aciduriaQ34263898
Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardationQ34574663
Neuropathological, biochemical and molecular findings in a glutaric acidemia type 1 cohortQ42473849
3-Hydroxyisobutyric aciduria: an inborn error of valine metabolismQ46049286
Evidence that 3-hydroxyisobutyric acid inhibits key enzymes of energy metabolism in cerebral cortex of young ratsQ46711572
Basal ganglia lesions in a patient with 3-hydroxyisobutyric aciduriaQ48531174
Septo-optic dysplasia with cerebellar hypoplasia in Cornelia de Lange syndromeQ48851956
3-hydroxyisobutyric aciduria with a mild clinical courseQ71755026
3-Hydroxyisobutyric aciduria in two brothersQ74502569
Clinical, biochemical, and molecular findings in three patients with 3-hydroxyisobutyric aciduriaQ24304109
Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduriaQ28320742
Dysmyelination in the brain of adolescents and young adults with maple syrup urine diseaseQ30925488
3-Hydroxyisobutyric aciduria: phenotypic heterogeneity within a single familyQ34083564
P433issue4
P921main subjectautopsyQ41482
P304page(s)483-486
P577publication date2009-07-01
P1433published inCanadian Journal of Neurological SciencesQ5030246
P1476titleNeuropathology of 3-hydroxyisobutyric aciduria, an autopsy case report
P478volume36