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Late-onset neuropathy and leukodystrophy revealing a peroxisomal biogenesis defect in two girls
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Atypical Refsum disease with pipecolic acidemia and abnormal catalase distribution.
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Clinical approach to inherited peroxisomal disorders: A series of 27 patients.
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Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease.
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Cell and tissue heterogeneity in peroxisomal patients
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PEROXISOME MOSAICISM IN THE LIVERS OF PEROXISOMAL DEFICIENCY PATIENTS.
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HUMAN LIVER PATHOLOGY IN PEROXISOMAL DISEASES - A REVIEW INCLUDING NOVEL DATA.
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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