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2. Cost-effectiveness of surgery for degenerative cervical myelopathy in the United Kingdom

4. Safety of Same-Day Discharge Posterior Lumbar Decompression and/or Discectomy: An Observational Study Using Administrative Data From England.

7. Tackling gaps in developing life-changing treatments for dementia

11. Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.

13. APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD)

20. Improving FPGA Performance and Area Using an Adaptive Logic Module

21. Supplemental Material - Safety of Same-Day Discharge Posterior Lumbar Decompression and/or Discectomy: An Observational Study Using Administrative Data From England

23. Improving Awareness Could Transform Outcomes in Degenerative Cervical Myelopathy [AO Spine RECODE-DCM Research Priority Number 1]

27. Prominent phenotypic variability associated with mutations in Progranulin

30. Efficient timing analysis with known false paths using Biclique covering

31. Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms

32. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative

33. Linkage disequilibrium and association of MAPT H1 in Parkinson disease

38. P003 - Bone Loss of Vertebral Bodies at the Operation Segment after Cervical Arthroplasty: A Potential Complication?

39. Improving FPGA Performance and Area Using an Adaptive Logic Module

41. Supplemental_digital_material - Contact Sports as a Risk Factor for Amyotrophic Lateral Sclerosis: A Systematic Review

42. Kinetic analysis of the mechanism of interaction of full-length TIMP-2 and gelatinase A: evidence for the existence of a low-affinity intermediate

43. Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

46. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

47. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

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