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28 results on '"Wang, Jian-She"'

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1. Analysis of long-term treatment effects of odevixibat on clinical outcomes in children with progressive familial intrahepatic cholestasis in odevixibat clinical studies vs external controls from the NAPPED database

2. Serum bile acids are associated with native liver survival in patients with Alagille syndrome: results from the GALA study group

3. Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants

4. Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency

5. Recurrent AKR1D1 c.580-13T>A Variant

6. Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency

9. NTCP Deficiency Causes Gallbladder Abnormalities in Mice and Human Beings

10. Clinical features and natural history of 1154 Alagille syndrome patients: results from the international multicenter GALA study group

11. The phenotype of compound heterozygous BSEP deficiency patients is determined by the combined residual function of the two ABCB11 mutations: results from the NAPPED consortium

12. PS-195-Predicting long-term outcome after surgical biliary diversion in Bsep-deficiency patients: Results from the NAPPED consortium

13. Increased sulfation of bile acids in mice and human subjects with sodium taurocholate cotransporting polypeptide deficiency

14. RINT1 Bi-allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities

15. PS-195-Predicting long-term outcome after surgical biliary diversion in Bsep-deficiency patients: Results from the NAPPED consortium

16. Biallelic Loss-of-Function ZFYVE19 Mutations Are Associated with Congenital Hepatic Fibrosis, Sclerosing Cholangiopathy, and High-GGT Cholestasis

18. Synthesis and properties of two tetrapus host molecules with fluorinated chains

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