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2. Börjeson–Forssman–Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new families

6. Higher dose corticosteroids in patients admitted to hospital with COVID-19 who are hypoxic but not requiring ventilatory support (RECOVERY): a randomised, controlled, open-label, platform trial

7. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

8. Baricitinib in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial and updated meta-analysis

11. Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine

16. Novel transglutaminases : a potential route to healthy skin

22. Reimagining health systems as systems for health

29. Effective post-pandemic governance must focus on shared challenges

30. Psychology, Law, and Criminal Justice

31. Project Town Gown

32. Prevalence and architecture of de novo mutations in developmental disorders

34. Children's Sexual Play and Behavior in Pre-School Settings: Staff's Perceptions, Reports, and Responses.

36. De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual Disability

38. ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism

41. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

48. Management of Sickle Cell Disease

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