Does enzyme replacement therapy influence the ocular changes in type VI mucopolysaccharidosis?

[1]  P. Harmatz,et al.  Reversed papilledema in an MPS VI patient with galsulfase (Naglazyme®) therapy , 2008, International Ophthalmology.

[2]  M. Beck,et al.  Ocular changes in patients with mucopolysaccharidosis I receiving enzyme replacement therapy: a 4-year experience. , 2007, Archives of ophthalmology.

[3]  G. Malm,et al.  Ocular findings in four children with mucopolysaccharidosis I-Hurler (MPS I-H) treated early with haematopoietic stem cell transplantation. , 2006, Acta ophthalmologica Scandinavica.

[4]  C. Eng,et al.  A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome) , 2006, Genetics in Medicine.

[5]  S. Biswas,et al.  The ocular features of the mucopolysaccharidoses , 2006, Eye.

[6]  J. Wittes,et al.  Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study. , 2006, The Journal of pediatrics.

[7]  M. Beck Galsulfase: enzyme-replacement therapy for mucopolysaccharidosis Type VI (Maroteaux–Lamy syndrome) , 2006 .

[8]  S. Biswas,et al.  Mucopolysaccharidoses and the eye. , 2006, Survey of ophthalmology.

[9]  F. Krummenauer,et al.  Cumulative incidence rates of the mucopolysaccharidoses in Germany , 2005, Journal of Inherited Metabolic Disease.

[10]  J. E. Wraith,et al.  The first 5years of clinical experience with laronidase enzyme replacement therapy for mucopolysaccharidosis I , 2005, Expert opinion on pharmacotherapy.

[11]  J. E. Wraith Enzyme replacement therapy in mucopolysaccharidosis type I: Progress and emerging difficulties , 2001, Journal of Inherited Metabolic Disease.

[12]  I. Süveges Histological and ultrastructural studies of the cornea in Maroteaux-Lamy syndrome , 1979, Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie.

[13]  S. Brodie,et al.  Long-term follow-up of corneal graft survival following bone marrow transplantation in the Maroteaux-Lamy syndrome. , 2001, The CLAO journal : official publication of the Contact Lens Association of Ophthalmologists, Inc.

[14]  J. Belmont,et al.  Enzyme-replacement therapy in mucopolysaccharidosis I. , 2001, The New England journal of medicine.

[15]  K. Ruprecht,et al.  Ocular Changes in Mucopolysaccharidosis IV A (Morquio A Syndrome) and Long-Term Results of Perforating Keratoplasty , 1999, Ophthalmologica.

[16]  C. Summers,et al.  Ocular abnormalities in the mucopolysaccharidoses after bone marrow transplantation. Longer follow-up. , 1998, Ophthalmology.

[17]  E. Cohen,et al.  Corneal transplantation in Maroteaux-Lamy syndrome. , 1997, Archives of ophthalmology.

[18]  U. Ramaswami,et al.  Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres , 1997, Archives of disease in childhood.

[19]  G. Naumann,et al.  Aufklaren der transplantatnahen Wirtshornhaut nach perforierender Keratoplastik beim Maroteaux-Lamy-Syndrom (Mukopolysaccharidose Typ VI-A) , 1993 .

[20]  G. Aguirre,et al.  Reciprocal corneal transplantation fails to correct mucopolysaccharidosis VI corneal storage. , 1992, Investigative ophthalmology & visual science.

[21]  B. Daicker,et al.  Simultane Hornhauttransplantation bei Mucopolysaccharidose , 1991 .

[22]  E. Traboulsi,et al.  Optic nerve head swelling and optic atrophy in the systemic mucopolysaccharidoses. , 1990, Ophthalmology.

[23]  L. Cantor,et al.  Glaucoma in the Maroteaux-Lamy syndrome. , 1989, American journal of ophthalmology.

[24]  R. Purple,et al.  Ocular changes in the mucopolysaccharidoses after bone marrow transplantation. A preliminary report. , 1989, Ophthalmology.

[25]  J. Stürmer Mukopolysaccharidose Typ VI-A (Morbus Maroteaux-Lamy) , 1989 .

[26]  M. Kaiser-Kupfer,et al.  Electroretinographic findings in the mucopolysaccharidoses. , 1986, Ophthalmology.

[27]  Green Wr,et al.  Occurrence of mucopolysaccharide in corneal grafts in the Maroteaux-Lamy syndrome. , 1985 .

[28]  W. Green,et al.  Ocular ultrastructural studies of two cases of the Hurler syndrome (systemic mucopolysaccharidosis I-H) * , 1983 .

[29]  R. Giugliani,et al.  The mucopolysaccharidoses. , 1976, Journal of medical genetics.