Show
Sort by
-
Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation
-
Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene.
-
Heterogeneity in primary hyperoxaluria type 1: morphometry and AGT-immunoreactivity of hepatic peroxisomes
-
Immunolocalization of a 43 kDA peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders
-
PEROXISOME MOSAICISM IN THE LIVERS OF PEROXISOMAL DEFICIENCY PATIENTS.
-
Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata
-
Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: A peroxisomal entity amenable to plasmapharesis. J. Inher. Metab. Dis., 15, 377-380, (1992).