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Your search keyword '"Mitchison, H"' showing total 193 results

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2. Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (Journal of Hepatology (2021) 75(3) (572–581), (S0168827821003342), (10.1016/j.jhep.2021.04.055))

3. Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (Journal of Hepatology (2021) 75(3) (572–581), (S0168827821003342), (10.1016/j.jhep.2021.04.055))

4. X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis

5. An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

8. Mutations in CCNO and MCIDAS lead to a mucociliary clearance disorder due to reduced generation of multiple motile cilia

9. X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis

20. The UK-PBC Risk Scores: Derivation and Validation of a Scoring System for Long-Term Prediction of End-Stage Liver Disease in Primary Biliary Cholangitis

22. Pretreatment prediction of response to ursodeoxycholic acid in primary biliary cholangitis: development and validation of the UDCA Response Score

23. A PROSPECTIVE AUDIT OF COLONOSCOPY IN A LARGE DGH--FACTORS EFFECTING CAECAL INTUBATION RATES

24. The UK-PBC risk scores: Derivation and validation of a scoring system for long-term prediction of end-stage liver disease in primary biliary cholangitis

25. Improving the efficiency of selection to Core Medical Training: a study of the use of multiple assessment stations

26. International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways

27. Gene discovery for motile cilia disorders: Mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151

28. Phenotypic variability of CCDC103 mutation in British Pakistani children with Primary Ciliary Dyskinesia (PCD)

29. A high-throughput genome-wide siRNA screen for ciliogenesis identifies new ciliary functional components and ciliopathy genes

30. Two week cancer guidelines: increased workload for no added benefit?

33. Mutations in the dynein assembly factor PF22 (DNAAF3) cause primary ciliary dyskinesia with absent dynein arms

35. Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes

38. DNAH3: Characterization of the sequence and mutation search in patients with Primary Ciliary Dyskinesia

40. Primary ciliary dyskinesia: current state of the art

45. Rapid diagnostic test for the major mutation underlying Batten disease

46. Autoimmune hepatitis (AIH), in men

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