GM1-gangliosidosis type I

British Journal of Haematology

Volumn 135, Issue 4, 2006, Pages 422-

  Pavlu, Jiri ^a   Jackson, Marie ^b   Panoskaltsis, Nicki ^c  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c NORTHWICK PARK HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GALACTOSIDASE; CHONDROITIN SULFATE; GANGLIOSIDE GM1; GLYCOSAMINOGLYCAN; HEPARAN SULFATE; KERATAN SULFATE;

ARTICLE; CASE REPORT; DEVELOPMENTAL DISORDER; ELECTROPHORESIS; EOSINOPHIL; FEMALE; GLOBOID CELL LEUKODYSTROPHY; GM1 GANGLIOSIDOSIS; HEPATOSPLENOMEGALY; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; MORQUIO SYNDROME; MUSCLE HYPOTONIA; PHYSICAL EXAMINATION; PRIORITY JOURNAL; URINALYSIS;

CYTOPLASMIC GRANULES; EOSINOPHILS; FEMALE; GANGLIOSIDOSIS, GM1; HUMANS; INFANT; LYMPHOCYTES;

EID: 33750068578     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2006.06287.x     Document Type: Article

References (1)

1. Giltzemann, R., Spycher, M.A., Adank, S., Baerlocher, K. & Steinmann, B. (1985) Anomalous eosinophil granulocytes in blood and bone marrow: a diagnostic marker for infantile GM1-gangliosidosis? European Journal of Pediatrics, 144, 82-84.