TREATMENT OF HURLER SYNDROME
- 1 October 1972
- journal article
- letter
- Published by Elsevier in The Lancet
- Vol. 300 (7782) , 883
- https://doi.org/10.1016/s0140-6736(72)92257-x
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Symptomatic pulmonary emphysema in childhood associated with hereditary alpha-1-antitrypsin and elastase inhibitor deficiencyThe Journal of Pediatrics, 1971
- Induced Degradation of Glycosaminoglycans in Hurler's and Hunter's Syndromes by Plasma InfusionProceedings of the National Academy of Sciences, 1971
- Deficiency of α1-Antitrypsin in Childhood Liver DiseasePediatrics, 1970
- CŒLIAC DISEASE AND SCHIZOPHRENIAThe Lancet, 1970