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Authors: Daniel H Wiseman; Jean Mercer; Karen Tylee; Nilima Malaiya; Denise K Bonney; Simon A Jones; J Edmond Wraith; Robert F Wynn
Journal: J Inherit Metab Dis Date: 2012-06-21 Impact factor: 4.982

6. Electrocardiographic and other cardiac anomalies in beta-glucuronidase-null mice corrected by nonablative neonatal marrow transplantation.

Authors: A J T Schuldt; T J Hampton; V Chu; C A Vogler; N Galvin; M D Lessard; J E Barker
Journal: Proc Natl Acad Sci U S A Date: 2004-01-02 Impact factor: 11.205

7. Retrovirally mediated overexpression of versican v3 reverses impaired elastogenesis and heightened proliferation exhibited by fibroblasts from Costello syndrome and Hurler disease patients.

Authors: Aleksander Hinek; Kathy R Braun; Kela Liu; Yanting Wang; Thomas N Wight
Journal: Am J Pathol Date: 2004-01 Impact factor: 4.307

Hurler syndrome with cardiomyopathy in infancy.

1. Impaired elastogenesis in Hurler disease: dermatan sulfate accumulation linked to deficiency in elastin-binding protein and elastic fiber assembly.

Review 2. The mucopolysaccharidoses: a clinical review and guide to management.

Review 3. Screening for lysosomal disorders.

Review 4. Metabolic cardiomyopathies.

5. Management of mucopolysaccharidosis type IH (Hurler's syndrome) presenting in infancy with severe dilated cardiomyopathy: a single institution's experience.

6. Electrocardiographic and other cardiac anomalies in beta-glucuronidase-null mice corrected by nonablative neonatal marrow transplantation.

7. Retrovirally mediated overexpression of versican v3 reverses impaired elastogenesis and heightened proliferation exhibited by fibroblasts from Costello syndrome and Hurler disease patients.

8. Glycosaminoglycan storage disorders: a review.

9. An algorithm to predict phenotypic severity in mucopolysaccharidosis type I in the first month of life.

Review 10. Mucopolysaccharidosis Type I: A Review of the Natural History and Molecular Pathology.