Gaucher disease
Definition:
References:
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[1]. Bryce A Heese, et al. Current strategies in the management of lysosomal storage diseases. Semin Pediatr Neurol. 2008 Sep;15(3):119-26. [Content Brief]
[2]. D Schnabel, et al. Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease. FEBS Lett. 1991 Jun 17;284(1):57-9. [Content Brief]
[3]. David A Wenger, et al. Insights into the diagnosis and treatment of lysosomal storage diseases. Arch Neurol. 2003 Mar;60(3):322-8. [Content Brief]
[4]. Ellen Sidransky, et al. Gaucher disease: complexity in a "simple" disorder. Mol Genet Metab. 2004 Sep-Oct;83(1-2):6-15. [Content Brief]
[5]. Hadhami Ben Turkia, et al. Velaglucerase alfa enzyme replacement therapy compared with imiglucerase in patients with Gaucher disease. Am J Hematol. 2013 Mar;88(3):179-84. [Content Brief]
[6]. Marina Jmoudiak, et al. Gaucher disease: pathological mechanisms and modern management. Br J Haematol. 2005 Apr;129(2):178-88. [Content Brief]
[7]. Terry D Butters, et al. Gaucher disease. Curr Opin Chem Biol. 2007 Aug;11(4):412-8. [Content Brief]
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