Plasma chitotriosidase activity in children with lysosomal storage disorders

Indian Journal of Pediatrics

Volumn 77, Issue 2, 2010, Pages 203-205

  Sheth, Jayesh J ^a   Sheth, Frenny J ^a   Za, Nrupesh J ^a   Gambhir, Prakash S ^b   Dave, Usha P ^c   Shah, Raju C ^d  

^a Institute of Human Genetics   (India)

^b Birthright Genetic Clinic   (India)

^c Khushaldas Dagra House   (India)

^d Ankur Neonatal Nursery   (India)

Author keywords

Chitotriosidase; Gaucher disease; Lysosomal storage disorders; Niemann Pick disease

Indexed keywords

BIOLOGICAL MARKER; CHITOTRIOSIDASE; LYSOSOME ENZYME;

ADOLESCENT; ARTICLE; BONE DYSPLASIA; CHILD; CONTROLLED STUDY; ENZYME ACTIVITY; FIBROBLAST; GAUCHER DISEASE; GLYCOGEN STORAGE DISEASE TYPE 2; GM2 GANGLIOSIDOSIS; HEPATOSPLENOMEGALY; HUMAN; INFANT; LEUKOCYTE; LYSOSOME STORAGE DISEASE; MACROPHAGE ACTIVATION; MAJOR CLINICAL STUDY; METACHROMATIC LEUKODYSTROPHY; MORQUIO SYNDROME; MUCOPOLYSACCHARIDOSIS TYPE 7; NIEMANN PICK DISEASE; PRESCHOOL CHILD; REMISSION; SANDHOFF DISEASE; SCHOOL CHILD;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; FEMALE; HEXOSAMINIDASES; HUMANS; INFANT; LYSOSOMAL STORAGE DISEASES; MALE;

EID: 77949267096     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12098-009-0249-0     Document Type: Article

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