Peroxisomal disorders: Classification and overview of biochemical abnormalities;Enfermedades peroxisomales: Clasificacion y descripcion de las anomalias bioquimicas

Revista de Neurologia

Volumn 28, Issue SUPPL. 1, 1999, Pages

  Moser, H W ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

Disorders of peroxisome biogenesis; Peroxisomal disorders; Zellweger syndrome

Indexed keywords

ADRENOLEUKODYSTROPHY; ARTICLE; CHONDRODYSPLASIA PUNCTATA; DISEASE CLASSIFICATION; DISORDERS OF PEROXISOMAL FUNCTIONS; HUMAN; INFANT; PEROXISOME; PRESCHOOL CHILD; PROTEIN DEFECT; REFSUM DISEASE; ZELLWEGER SYNDROME; BIOGENESIS; BLOOD; CLASSIFICATION; FEMALE; GENOTYPE; MALE; NEWBORN; PHENOTYPE; REVIEW;

BIOGENESIS; CHILD, PRESCHOOL; FEMALE; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; MALE; PEROXISOMAL DISORDERS; PHENOTYPE;

EID: 0033367858     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (3)

1. Evrard P, Caviness VS, Prats-Viñas J, Lyon G. The mechanism of arrest of neuronal migration in the Zellweger malformation: an hypothesis based upon cytoarchitectonic analysis. Acta Neuropathol (Berl) 1978; 41: 109-17.
2. Roels F, Goldfischer S. Cytochemistry of human catalase. The demonstration of hepatic and renal peroxisomes by a high temperature procedure. J Histochem Cytochem 1979; 27: 1471-7.
3. Goldfischer S, Moore CL, Johnson AB, Spiro AJ, Valsamis MP, Ritch RH, et al. Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome. Science 1973; 182: 62-4.