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Defective protein glycosylation in patients with cutis laxa syndrome
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Morphometry and AGT-immunoreactivity of hepatic peroxisomes: heterogeneity in primary hyperoxaluria type 1
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Cell and tissue heterogeneity in peroxisomal patients
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Cytoplasmic catalase and ghost-like hepatic peroxisomes in a child with bone dysplasia and mental retardation
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Mosaicism of hepatic peroxisome distribution in peroxisomal patients
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Catalase deficient, giant hepatic peroxisomes containing four other enzymes in a child with bone dysplasia
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Catalase deficient, giant hepatic peroxisomes containing four other enzymes in a child with bone dysplasia
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Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: A peroxisomal entity amenable to plasmapharesis
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Giant, catalase deficient hepatic peroxisomes in a child with bone dysplasia, impaired plasmogcn synthesis and phytanic acid storage
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Cell and Tissue heterogeneiry in peroxisomal patients. Kon. Ned. Akademie van Wetenschappen. 'Peroxisomal disorders in relation to functions and biogenesis of peroxisomes', Colloquium Amsterdam 18-19 October 1993.