Ocular Histopathology of Systemic Mucopolysaccharidosis, Type II-A (Hunter Syndrome, Severe)
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference23 articles.
1. The mucopolysaccharide storage diseases;McKusick,1983
2. Ocular ultrastructural studies of two cases of the Hurler syndrome (systemic mucopolysaccharidosis I-H);Chan;Ophthalmic Paediatr Genet,1983
3. Scheie syndrome and macular corneal dystrophy; an ultrastructural comparison of conjunctiva and skin;Quigley;Arch Ophthalmol,1971
4. Ultrastructural ocular pathology of Hunter's syndrome; systemic mucopolysaccharidosis type II;Topping;Arch Ophthalmol,1971
5. Histopathology of Sanfilippo's syndrome;Del Monte;Arch Ophthalmol,1983
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1. Expanding the phenotype of mucopolysaccharidosis type II retinopathy;Ophthalmic Genetics;2021-07-12
2. Anterior Chamber Angles in Different Types of Mucopolysaccharidoses;American Journal of Ophthalmology;2020-04
3. Recovery of Vision following Enzyme Replacement Therapy in a Patient with Mucopolysaccharidosis Type II, Hunter Syndrome;Case Reports in Ophthalmology;2019-06-06
4. Early Retinal Changes in Hunter Syndrome According to Spectral Domain Optical Coherence Tomography;Korean Journal of Ophthalmology;2016
5. Spectral domain optical coherence tomography imaging of mucopolysaccharidoses I, II, and VI A;Graefe's Archive for Clinical and Experimental Ophthalmology;2015-02-18
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