Alpha1-Antitrypsin Phenotype: Transient Cathodal Shift in Serum of Infant Girl with Urinary Cytomegalovirus and Fatty Liver
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Cited by 20 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. Unusually difficult clinical presentation of an infant suffering from congenital cytomegalovirus (CMV) infection combined with alpha 1-antitrypsin (A1AT) deficiency;Biochemia Medica;2014
2. α1-Antitrypsinmangel;Der Internist;2010-02-06
3. Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS;Human Mutation;2000
4. Differential Metabolism of Tetrahydrobiopterin in Monoamine Neurons: A Hypothese Based upon Clinical and Basic Research;Advances in Experimental Medicine and Biology;1993
5. Transient aberrancy of α1-antitrypsin glycoprotein microheterogeneity in Pseudomonas aeruginosa septicaemia;Infection;1990-11
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