Author:
Obaid Abdulrahman,Nashabat Marwan,Al Fakeeh Khalid,Al Qahtani Abdullah T.,Alfadhel Majid
Publisher
Springer Science and Business Media LLC
Reference19 articles.
1. Andreassen KH, Pedersen KV, Osther SS, Jung HU, Lildal SK, Osther PJ. How should patients with cystine stone disease be evaluated and treated in the twenty-first century? Urolithiasis. 2016;44(1):65–76.
2. Knoll T, Zollner A, Wendt-Nordahl G, Michel MS, Alken P. Cystinuria in childhood and adolescence: recommendations for diagnosis, treatment, and follow-up. Pediatr Nephrol. 2005;20(1):19–24.
3. Gitomer WL, Reed BY, Ruml LA, Skhaee K, Pak CYC. Mutations in the genomic deoxyribonucleic acid for SLC3A1 in patients with cystinuria. J Clin Endocrinol Metab. 1998;83(10):3688–94.
4. Alfadhel M, Benmeakel M, Hossain MA, Al Mutairi F, Al Othaim A, Alfares AA, Al Balwi M, Alzaben A, Eyaid W. Thirteen year retrospective review of the spectrum of inborn errors of metabolism presenting in a tertiary center in Saudi Arabia. Orphanet J Rare Dis. 2016;11(1):126.
5. Eggermann T, Venghaus A, Zerres K: Cystinuria: an inborn cause of urolithiasis. Orphanet Journal of Rare Diseases 2012, 7(19).
Cited by
6 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