Ocular findings and their correlation with disease severity in Fabry disease in South-East Anatolia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
https://link.springer.com/content/pdf/10.1007/s10792-022-02626-6.pdf
Reference37 articles.
1. Germain DP (2010) Fabry disease. Orphanet J Rare Dis 5(1):30
2. Desnick RJ (2015) Chapter 38—Fabry Disease: α-Galactosidase A deficiency. In: Rosenberg RN, Pascual JM (eds) Rosenberg’s molecular and genetic basis of neurological and psychiatric disease, 5th edn. Academic Press, Boston, pp 419–430
3. Desnick RJ et al (1980) Enzyme therapy XVII: metabolic and immunologic evaluation of alpha-galactosidase a replacement in Fabry disease. Birth Defects Orig Artic Ser 16(1):393–413
4. El-Abassi R, Singhal D, England JD (2014) Fabry’s disease. J Neurol Sci 344(1):5–19
5. Bacherini D et al (2021) Optical coherence tomography angiography for the evaluation of retinal vasculature in fabry disease: our experience and review of current knowledge. Front Neurol 12:640719
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