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3. Conformational fingerprinting with Raman spectroscopy reveals protein structure as a translational biomarker of muscle pathology

12. Non‐negative matrix factorisation of Raman spectra finds common patterns relating to neuromuscular disease across differing equipment configurations, preclinical models and human tissue

14. Reinnervation as measured by the motor unit size index is associated with preservation of muscle strength in amyotrophic lateral sclerosis, but not all muscles reinnervate

15. Rapid identification of human muscle disease with fibre optic Raman spectroscopy

17. Non‐negative matrix factorisation of Raman spectra finds common patterns relating to neuromuscular disease across differing equipment configurations, preclinical models and human tissue.

18. Reinnervation as measured by the motor unit size index is associated with preservation of muscle strength in amyotrophic lateral sclerosis, but not all muscles reinnervate

19. The application of Raman spectroscopy to the diagnosis of mitochondrial muscle disease: A preliminary comparison between fibre optic probe and microscope formats

23. In Vivo Fiber Optic Raman Spectroscopy of Muscle in Preclinical Models of Amyotrophic Lateral Sclerosis and Duchenne Muscular Dystrophy

27. Simultaneous ALS and SCA2 associated with an intermediate-length ATXN2 CAG-repeat expansion

29. The application of Raman spectroscopy to the diagnosis of mitochondrial muscle disease: A preliminary comparison between fibre optic probe and microscope formats.

32. Assessment of the reliability of the motor unit size index (MUSIX) in single subject 'round-robin' and multi-centre settings

33. Simultaneous ALS and SCA2 associated with an intermediate-length ATXN2 CAG-repeat expansion.

34. The GLP-1 receptor agonist, liraglutide, fails to slow disease progression in SOD1G93A and TDP-43Q331K transgenic mouse models of ALS.

35. Extensive phenotypic characterisation of a human TDP-43Q331K transgenic mouse model of amyotrophic lateral sclerosis (ALS).

38. Biomarkers in Motor Neuron Disease: A State of the Art Review

42. Imaging muscle as a potential biomarker of denervation in motor neuron disease

43. Sleep deprivation and melatonin for inducing sleep in paediatric electroencephalography: a prospective multicentre service evaluation.

44. Imaging muscle as a potential biomarker of denervation in motor neuron disease.

46. Extreme sensitivity of myelinating optic nerve axons in a rodent model of perinatal ischemic injury

47. Vesicular apparatus, including functional calcium channels, are present in developing rodent optic nerve axons and are required for normal node of Ranvier formation

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