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Publications by Ines M Lanzl

Ocular Features of Treatable Lysosomal Storage Disorders—Fabry Disease, Mucopolysaccharidoses I, II and VI and Gaucher Disease

US Ophthalmic Review

English

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Ocular Manifestations and Management Recommendations of Lysosomal Storage Disorders I: Mucopolysaccharidoses

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Lysosomal Storage Disease: Revealing Lysosomal Function and Physiology

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Pathologic Studies of Lysosomal Storage Disease.

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Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease

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Quantitative Estimation of Lysosomal Storage in Mucopolysaccharidoses by Electron Microscopy Analysis.

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46. Classic Histological Features of Gaucher Disease: A Case Report

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Gaucher Disease Type I Complicated With Parkinson's Syndrome

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Fabry Disease

Revista de la Facultad de Medicina Humana

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