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Publications by Shoju ONISHI
The First Case of Crigler-Najjar Syndrome Type-1 in Japan
Acta Hepatologica Japonica
Hepatology
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A Novel Pathogenic UGT1A1 Variant in a Sudanese Child With Type I Crigler-Najjar Syndrome
Drug Metabolism and Disposition
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Identification of a Novel Deletion in UDP-glucuronosyltransferase Gene in a Patient With Crigler–Najjar Syndrome Type I
Blood Cells, Molecules, and Diseases
Molecular Medicine
Hematology
Molecular Biology
Cell Biology
Reduction of Hyperbilirubinemia With Hypericum Extract (St. John's Wort) in a Patient With Crigler-Najjar Syndrome Type II
British Journal of Clinical Pharmacology
Pharmacology
Two Unrelated Patients With Rare Crigler-Najjar Syndrome Type I: Two Novel Mutations and a Patient With Loss of Heterozygosity of UGT1A1 Gene
Journal of Zhejiang University: Science B
Genetics
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Molecular Biology
Biochemistry
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Toxicology
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Discrimination Between Crigler-Najjar Type I and II by Expression of Mutant Bilirubin Uridine Diphosphate-Glucuronosyltransferase.
Journal of Clinical Investigation
Medicine
UGT1a1 Gene Mutations in a Tibetan Patient With Crigler-Najjar SyndromeType II - Case Report and Literature Review
Current Trends in Clinical & Medical Imaging
Identification of a Genetic Alteration in the Code for Bilirubin UDP-glucuronosyltransferase in the UGT1 Gene Complex of a Crigler-Najjar Type I Patient.
Journal of Clinical Investigation
Medicine
Compound Heterozygosity of a Novel Exon 3 Frameshift (p.R357P Fs*24) Mutation and Y486D Mutation in Exon 5 of the UGT1A1 Gene in a Thai Infant With Crigler-Najjar Syndrome Type 2
Genetics and Molecular Research
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Waardenburg Syndrome Type 1: Case Report
The Journal of Kartal Training and Research Hospital
