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Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: Clinical presentation, metabolic and histological findings.
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Long survival in a case of peroxisomal biogenesis disorder with peroxisome mosaicism in the liver.
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PEROXISOME MOSAICISM IN THE LIVERS OF PEROXISOMAL DEFICIENCY PATIENTS.
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A new type of peroxisomal disorder with variable expression in liver and fibroblasts.
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Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata
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Peroxisomes are enlarged in two patients with peroxisomal diseases: novel cases
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Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency) : novel data
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Post-mortem visualization of peroxisomes in rat and in human liver