A review of type 3 Gaucher disease: unique neurological manifestations and advances in treatment
Author:
Funder
Medical Science and Technology Project of Zhejiang Province
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s13760-024-02493-1.pdf
Reference98 articles.
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3. Grabowski GA (2008) Phenotype, diagnosis, and treatment of Gaucher’s disease. Lancet 372:1263–1271. https://doi.org/10.1016/s0140-6736(08)61522-6
4. Gary SE, Ryan E, Steward AM, Sidransky E (2018) Recent advances in the diagnosis and management of Gaucher disease. Expert Rev Endocrinol Metab 13:107–118. https://doi.org/10.1080/17446651.2018.1445524
5. Goker-Alpan O, Schiffmann R, Park JK et al (2003) Phenotypic continuum in neuronopathic Gaucher disease: an intermediate phenotype between type 2 and type 3. J Pediatr 143:273–276. https://doi.org/10.1067/s0022-3476(03)00302-0
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