4.1 Article

Massive Accumulation of Glycosaminoglycans in the Aortic Valve of a Patient With Hunter Syndrome During Enzyme Replacement Therapy

Related references

Note: Only part of the references are listed.
Review Endocrinology & Metabolism

Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management

Elizabeth A. Braunlin et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2011)

Article Cardiac & Cardiovascular Systems

The natural course and the impact of therapies of cardiac involvement in the mucopolysaccharidoses

Vlasta Fesslova et al.

CARDIOLOGY IN THE YOUNG (2009)

Article Cardiac & Cardiovascular Systems

Mitral Valve Replacement and Hunter Syndrome: Case Report

Theophani Antoniou et al.

HEART SURGERY FORUM (2009)

Review Pediatrics

Multidisciplinary Management of Hunter Syndrome

Joseph Muenzer et al.

PEDIATRICS (2009)

Article Genetics & Heredity

Initial report from the Hunter Outcome Survey

J. Edmond Wraith et al.

GENETICS IN MEDICINE (2008)

Article Endocrinology & Metabolism

A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome)

Joseph Muenzer et al.

MOLECULAR GENETICS AND METABOLISM (2007)

Article Cardiac & Cardiovascular Systems

Mitral valve replacement for mitral stenosis secondary to Hunter's syndrome

K Bhattacharya et al.

ANNALS OF THORACIC SURGERY (2005)