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2. Bodipy-based dyes for ionic-liquid-based optical carbon dioxide sensors

5. Study methodology and insights from the palovarotene clinical development program in fibrodysplasia ossificans progressiva

9. True self-reinforced composites enabled by tuning of molecular structure for lightweight structural materials in future mobility

11. Reduction of New Heterotopic Ossification ( HO ) in the Open‐Label , Phase 3 MOVE Trial of Palovarotene for Fibrodysplasia Ossificans Progressiva ( FOP )

12. The effects of palovarotene in patients with fibrodysplasia ossificans progressiva: a plain language summary

14. Growth parameters in children with achondroplasia: A 7-year, prospective, multinational, observational study

15. The natural history of fibrodysplasia ossificans progressiva: A prospective, global 36-month study

17. Effects of Nitisinone on Oxidative and Inflammatory Markers in Alkaptonuria: Results from SONIA1 and SONIA2 Studies

23. A natural history study of fibrodysplasia ossificans progressiva (FOP): 12-month outcome results

24. Efficacy and safety of once-daily nitisinone for patients with alkaptonuria (SONIA 2): an international, multicentre, open-label, randomised controlled trial

25. A global natural history study of Fibrodysplasia Ossificans Progressiva (FOP): 12-month outcomes

26. Patients with ACVR1R206H mutations have an increased prevalence of cardiac conduction abnormalities on electrocardiogram in a natural history study of Fibrodysplasia Ossificans Progressiva

28. Homogentisic acid is not only eliminated by glomerular filtration and tubular secretion but also produced in the kidney in alkaptonuria

29. Growth charts in Kabuki syndrome 1

31. C-Type Natriuretic Peptide Analogue Therapy in Children with Achondroplasia

32. Correction to: Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes

33. Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes

35. Anatomical and functional abnormalities on MRI in kabuki syndrome

41. Prevalence of fibrodysplasia ossificans progressiva (FOP) in France: an estimate based on a record linkage of two national databases

43. Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation study

45. Mutation Update for Kabuki Syndrome GenesKMT2DandKDM6Aand Further Delineation of X-Linked Kabuki Syndrome Subtype 2

46. The Performance of a Modified Glasgow Blatchford Score in Predicting Clinical Interventions in Patients with Acute Nonvariceal Upper Gastrointestinal Bleeding: A Vietnamese Prospective Multicenter Cohort Study

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