455 results on '"Wang, Jian-She"'
Search Results
2. Diagnosis, treatment and prevention of severe acute respiratory syndrome coronavirus 2 infection in children: experts’ consensus statement updated for the Omicron variant
3. Efficacy of rituximab-containing regimens used as first-line and rescue therapy for giant cell hepatitis with autoimmune hemolytic anemia a retrospective study
4. Poly-hydroxylated bile acids and their prognostic roles in Alagille syndrome
5. Impact of genetic and non-genetic factors on phenotypic diversity in NBAS-associated disease
6. Diagnosis, treatment, and prevention of monkeypox in children: an experts’ consensus statement
7. Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants
8. Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency
9. Neonatal cholestasis is an early liver manifestation of children with acid sphingomyelinase deficiency
10. Kinesin family member 12‐related hepatopathy: A generally indolent disorder with elevated gamma‐glutamyl‐transferase activity.
11. NTCP Deficiency Causes Gallbladder Abnormalities in Mice and Human Beings
12. Cholestasis as a dominating symptom of patients with CYP27A1 mutations: An analysis of 17 Chinese infants
13. Genotype correlates with the natural history of severe bile salt export pump deficiency
14. Transcript selection for the genetic diagnosis of KIF12-associated progressive familial intrahepatic cholestasis
15. A new immune-related gene signature predicts the prognosis and immune escape of bladder cancer
16. Comprehensive analysis of integrin αvβ3/α6β1 in prognosis and immune escape of prostate cancer
17. Prevention of Portal-Tract Fibrosis in Zfyve19−/− Mouse Model with Adeno-Associated Virus Vector Delivering ZFYVE19
18. Non-invasive biomarkers for identification of vanishing bile duct syndrome among children with acute cholestatic hepatitis
19. Genetic spectrum and clinical characteristics of 3β-hydroxy-Δ5-C27-steroid oxidoreductase (HSD3B7) deficiency in China
20. Successful treatment of infantile oxysterol 7α-hydroxylase deficiency with oral chenodeoxycholic acid
21. Novel NGLY1 gene variants in Chinese children with global developmental delay, microcephaly, hypotonia, hypertransaminasemia, alacrimia, and feeding difficulty
22. Molecular findings in children with inherited intrahepatic cholestasis
23. Heat shock protein family A member 8 is a prognostic marker for bladder cancer: Evidences based on experiments and machine learning
24. Comprehensive Bile Acid Profiling of ABCB4-mutated Patients and the Prognostic Role of Taurine-conjugated 3α,6α,7α,12α-Tetrahydroxylated Bile Acid in Cholestasis
25. P1 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
26. Abnormal Bilirubin Metabolism in Patients with Sodium Taurocholate Cotransporting Polypeptide Deficiency
27. 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
28. Serum bile acids are associated with native liver survival in patients with Alagille syndrome: results from the GALA study group
29. Abnormal Bilirubin Metabolism in Patients With Sodium Taurocholate Cotransporting Polypeptide Deficiency
30. Risk factors associated with mortality in neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) and clinical implications
31. Prevention of Portal-Tract Fibrosis in Zfyve19−/− Mouse Model with Adeno-Associated Virus Vector Delivering ZFYVE19.
32. Wilson Disease in China
33. List of Contributors
34. Neonatal sclerosing cholangitis with novel mutations in DCDC2 (doublecortin domain-containing protein 2) in Chinese children
35. Recurrent AKR1D1 c.580-13T>A Variant
36. Synergistic photocatalysis of Cr(VI) reduction and 4-Chlorophenol degradation over hydroxylated α-Fe2O3 under visible light irradiation
37. Balanced Translocation Disrupting JAG1 Identified by Optical Genomic Mapping in Suspected Alagille Syndrome
38. Anemia following zinc treatment for Wilson’s disease: a case report and literature review
39. Ursodeoxycholic acid administration did not reduce susceptibility to SARS‐CoV‐2 infection in children.
40. Splicing Analysis of MYO5B Noncanonical Variants in Patients with Low Gamma-Glutamyltransferase Cholestasis.
41. Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease
42. UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation
43. Glycogen storage disease type Ia misdiagnosed as multiple acyl-coenzyme A dehydrogenase deficiency by mass spectrometry
44. THU-291 - Serum bile acids are associated with native liver survival in patients with Alagille syndrome: results from the GALA study group
45. Updated clinical and glycomic features of mannosyl-oligosaccharide glucosidase deficiency: Two case reports
46. Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass Spectrometry
47. A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report
48. Association of novel TMEM67 variants with mild phenotypes of high gamma‐glutamyl transpeptidase cholestasis and congenital hepatic fibrosis
49. Defining pathogenicity ofNOTCH2variants for diagnosis of Alagille syndrome type 2 using a large cohort of patients
50. Poly-hydroxylated bile acids and their prognostic roles in Alagille syndrome
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.