A Rare Cause of Neonatal Liver Failure
Author:
Publisher
Jaypee Brothers Medical Publishing
Link
https://www.apgh.net/doi/pdf/10.5005/jp-journals-11009-0151
Reference7 articles.
1. 1. Richards S, Aziz N, Bale S, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015;17(5):405–424. DOI: 10.1038/gim.2015.30
2. 2. Geberhiwot T, Moro A, Dardis A, et al. Consensus clinical management guidelines for Niemann–Pick disease type C. Orphanet J Rare Dis 2018;13(1):50. DOI: 10.1186/s13023-018-0785-7
3. 3. Lipinski P, Jankowska I, Lugowska A, et al. Newborn presentation of Niemann–Pick disease type C – difficulties and limitations of diagnostic methods. Pediatr Neonatol 2018;59(3):317–318. DOI: 10.1016/j.pedneo.2017.09.003
4. 4. Sundaram SS, Alonso EM, Narkewicz MR, et al. Characterization and outcomes of young infants with acute liver failure. J Pediatr 2011;159(5):813–818. DOI: 10.1016/j.jpeds.2011.04.016
5. 5. Rodrigues AF, Gray RG, Preece MA, et al. The usefulness of bone marrow aspiration in the diagnosis of Niemann–Pick disease type C in infantile liver disease. Arch Dis Child 2006;91(10):841–844. DOI: 10.1136/adc.2005.088013
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