The role of automated analyzers in detecting abnormal granulation of leucocytes in lysosomal storage diseases: Maroteaux-Lamy disease
Author:
Affiliation:
1. Department of Laboratory Medicine; Padua University School of Medicine; Padua; Italy
2. Metabolic Disorders Unit of the Department of Pediatrics; University of Padua; Padua; Italy
Publisher
Wiley
Subject
Hematology
Reference5 articles.
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2. Expert recommendations for the laboratory diagnosis of MPS VI;Wood;Mol Genet Metab,2012
3. Mucopolysaccharidosis VI;Valayannopoulos;Orphanet J Rare Dis,2010
4. An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum;Brooks;Mol Genet Metab,2005
5. Braunlin E Rosenfeld H Kampmann C MPS VI Study Group. Enzyme replacement therapy for mucopolysaccharidosis VI Long-term cardiac effects of galsulfase (Naglazyme®) therapy J Inherit Metab Dis. 2012; [Epub ahead of print]
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