18 results on '"Stapelbroek, Janneke M."'
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2. Farnesoid X receptor (FXR) activation and FXR genetic variation in inflammatory bowel disease.
3. ATP8B1 Is Essential for Maintaining Normal Hearing
4. Familial cholestasis: Progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy
5. Neither inflammatory bowel disease nor immunosuppressants are associated with an increased risk of severe COVID-19: an observational Dutch cohort study
6. Paraneoplastic pemphigus associated with post‐transplant lymphoproliferative disorder after small bowel transplantation
7. Folding Defects in P-Type Atp 8B1 Associated With Hereditary Cholestasis Are Ameliorated by 4-Phenylbutyrate
8. The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis
9. Loss of syntaxin 3 causes variant microvillus inclusion disease
10. Loss of Syntaxin 3 Causes Variant Microvillus Inclusion Disease
11. Mutational Analysis of ATP8B1 in Patients with Chronic Pancreatitis
12. Liver disease associated with canalicular transport defects: Current and future therapies
13. Folding defects in P-type ATP 8B1 associated with hereditary cholestasis are ameliorated by 4-phenylbutyrate
14. Reduced expression of ATP7B affected by Wilson disease-causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin
15. Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis
16. Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis–renal dysfunction–cholestasis (ARC) syndrome
17. Mutational Analysis of ATP8B1 in Patients with Chronic Pancreatitis.
18. Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis.
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