Neuronopathic lysosomal storage diseases: Clinical and pathologic findings

Author:

Prada Carlos E.,Grabowski Gregory A.1

Affiliation:

1. Division of Human Genetics; Department of Pediatrics, Cincinnati Children's Hospital Medical Center; Cincinnati; Ohio

Publisher

Wiley

Subject

Psychiatry and Mental health,Developmental and Educational Psychology,Pediatrics, Perinatology and Child Health

Reference174 articles.

1. Neuropsychological symptoms of juvenile-onset batten disease: experiences from 2 studies;Adams;J Child Neurol,2007

2. Neurological findings in Hunter disease: pathology and possible therapeutic effects reviewed;Al Sawaf;J Inherit Metab Dis,2008

3. Progressive nature of aspartylglucosaminuria;Arvio;Acta Paediatr,2002

4. Overgrowth of oral mucosa and facial skin, a novel feature of aspartylglucosaminuria;Arvio;J Med Genet,1999

5. Excessive infantile growth and early pubertal growth spurt: typical features in patients with aspartylglycosaminuria;Arvio;J Pediatr.,1999

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