Author:
Abu-Asab Mones S.,Yeung Ian Y. L.,Ardeljan Christopher,Gonzalez Ashley N.,Sidransky Ellen,Chan Chi-Chao
Reference54 articles.
1. Alfonso P, Aznarez S, Giralt M, Pocovi M, Giraldo P. Mutation analysis and genotype/phenotype relationships of Gaucher disease patients in Spain. J Hum Genet. 2007;52(5):391–6.
2. Baris HN, Cohen IJ, Mistry PK. Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history. Pediatr Endocrinol Rev. 2014;12(Suppl 1):72–81.
3. Beavan M, McNeill A, Proukakis C, Hughes DA, Mehta A, Schapira AH. Evolution of prodromal clinical markers of parkinson disease in a GBA mutation-positive cohort. JAMA Neurol. 2015;72(2):201–8.
4. Bruscolini A, Pirraglia MP, Restivo L, Spinucci G, Abbouda A. A branch retinal artery occlusion in a patient with Gaucher disease. Graefes Arch Clin Exp Ophthalmol. 2012;250(3):441–4.
5. Cassinerio E, Graziadei G, Poggiali E. Gaucher disease: a diagnostic challenge for internists. Eur J Intern Med. 2014;25(2):117–24.
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献