Kernicterus in an adult who is heterozygous for Crigler-Najjar syndrome and homozygous for Gilbert-type genetic defect.
about
Inherited disorders of bilirubin clearanceGenetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotypeQuantitative assessment of the multiple processes responsible for bilirubin homeostasis in health and disease.Pharmacogenomics of human UDP-glucuronosyltransferase enzymes.Prediction of deleterious non-synonymous single-nucleotide polymorphisms of human uridine diphosphate glucuronosyltransferase genes.Crigler-Najjar syndrome type 2: Novel UGT1A1 mutationSuccessful plasmapheresis for acute and severe unconjugated hyperbilirubinemia in a child with crigler najjar type I syndrome.
P2860
Q26776470-D132372E-AB23-4670-97CE-B3512E658FA1Q28140057-F160136F-55F6-41FE-9ED3-3B25E496B652Q34155271-9E6A3EB5-548A-4224-A573-8A6A8CB7A5D1Q35157993-F6FF99D3-A488-4076-9FE2-C678A14B6305Q37378051-17B17E87-B98F-446E-8CB8-EC848799482CQ41433988-E4149E63-724B-4CEA-A51D-5B6B1F40F4BFQ41967780-BADB9DA1-15F2-4EC1-AD3D-E69C098ACCFC
P2860
Kernicterus in an adult who is heterozygous for Crigler-Najjar syndrome and homozygous for Gilbert-type genetic defect.
description
1997 nî lūn-bûn
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1997年の論文
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1997年学术文章
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name
Kernicterus in an adult who is ...... r Gilbert-type genetic defect.
@en
Kernicterus in an adult who is ...... r Gilbert-type genetic defect.
@nl
type
label
Kernicterus in an adult who is ...... r Gilbert-type genetic defect.
@en
Kernicterus in an adult who is ...... r Gilbert-type genetic defect.
@nl
prefLabel
Kernicterus in an adult who is ...... r Gilbert-type genetic defect.
@en
Kernicterus in an adult who is ...... r Gilbert-type genetic defect.
@nl
P2093
P1433
P1476
Kernicterus in an adult who is ...... r Gilbert-type genetic defect.
@en
P2093
Chalasani N
Chowdhury JR
Chowdhury NR
P304
P356
10.1053/GAST.1997.V112.PM9178703
P407
P577
1997-06-01T00:00:00Z