Plasma lysosomal enzyme activities in congenital disorders of glycosylation, galactosemia and fructosemia

Clinica Chimica Acta

Volumn 401, Issue 1-2, 2009, Pages 81-83

  Michelakakis, Helen ^a   Moraitou, Marina ^a   Mavridou, Irene ^a   Dimitriou, Evangelia ^a  

^a Institute of Child Health Athens gr   (Greece)

Author keywords

Congenital disorders of glycosylation; Lysosomal enzymes

Indexed keywords

ALPHA MANNOSIDASE; BETA MANNOSIDASE; BETA N ACETYLHEXOSAMINIDASE; LYSOSOME ENZYME; N4 (BETA N ACETYLGLUCOSAMINYL)ASPARAGINASE;

ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; DIET THERAPY; DISEASE MARKER; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; GALACTOSEMIA; GLYCOSYLATION; HEREDITARY FRUCTOSE INTOLERANCE; HUMAN; INFANT; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; TREATMENT RESPONSE;

ADOLESCENT; ALPHA-MANNOSIDASE; ASPARTYLGLUCOSYLAMINASE; BETA-MANNOSIDASE; BETA-N-ACETYLHEXOSAMINIDASES; CHILD; CHILD, PRESCHOOL; FRUCTOSE INTOLERANCE; FRUCTOSE METABOLISM, INBORN ERRORS; GALACTOSEMIAS; GLYCOSYLATION; HUMANS; INFANT; LYSOSOMES;

EID: 58549093252     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cca.2008.11.024     Document Type: Article

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