Author:
Boquist Lennart,Lindqvist Bengt,Östberg Yngve,Steen Lars
Reference25 articles.
1. Familial hyperoxaluria. Report of a family; review of the literature;Daniels;Amer J Med,1960
2. L-glyceric aciduria. A new genetic variant of primary hyperoxaluria;Williams;New Eng J Med,1968
3. Oxalose. Klinisches Bild, morphologische Befunde, pathogenetische Probleme;Gasser;Deutsch Arch Klin Med,1964
4. Primary hyperoxaluria and oxalosis, The Metabolic Basis of Inherited Disease;Wyngaarden,1966
5. Disorders of oxalate metabolism;Williams;Amer J Med,1968
Cited by
57 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
1. Advanced type 1 hyperoxaluria presenting as livedo racemosa in a patient with end-stage renal disease;Indian Journal of Dermatology, Venereology and Leprology;2019
2. Retinal flecks, dots and crystals;Taylor and Hoyt's Pediatric Ophthalmology and Strabismus;2017
3. Reversible diffuse arterial spasm in a patient with primary oxalosis;Turkish Journal of Thoracic and Cardiovascular Surgery;2013-03-20
4. Flecked retina disorders;Pediatric Ophthalmology and Strabismus;2013
5. Methanol and Ethylene Glycol Intoxication;Critical Care Clinics;2012-10