174 results on '"Alix, James J. P."'
Search Results
2. Hyperexcitability of the asymptomatic motor cortex in a case of Mills' syndrome
3. Conformational fingerprinting with Raman spectroscopy reveals protein structure as a translational biomarker of muscle pathology
4. Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease
5. Extensive phenotypic characterisation of a human TDP-43Q331K transgenic mouse model of amyotrophic lateral sclerosis (ALS)
6. Author Correction: Female sex mitigates motor and behavioural phenotypes in TDP-43Q331K knock-in mice
7. The GLP-1 receptor agonist, liraglutide, fails to slow disease progression in SOD1G93A and TDP-43Q331K transgenic mouse models of ALS
8. Combining electromyography and Raman spectroscopy: optical EMG
9. Female sex mitigates motor and behavioural phenotypes in TDP-43Q331K knock-in mice
10. Investigating and managing neonatal seizures in the UK: an explanatory sequential mixed methods approach
11. Correction to: Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease
12. Non‐negative matrix factorisation of Raman spectra finds common patterns relating to neuromuscular disease across differing equipment configurations, preclinical models and human tissue
13. Fiber optic Raman spectroscopy for the evaluation of disease state in Duchenne muscular dystrophy: An assessment using the mdx model and human muscle
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
16. Label-free fibre optic Raman spectroscopy with bounded simplex-structured matrix factorization for the serial study of serum in amyotrophic lateral sclerosis
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
20. Circuit Architecture for Electrical Impedance Spectroscopy Instrumentation to Address Electrode Impedance Mismatch in Clinical Devices
21. Tensor electrical impedance myography identifies clinically relevant features in amyotrophic lateral sclerosis
22. Neonatal seizures—part 2: Aetiology of acute symptomatic seizures, treatments and the neonatal epilepsy syndromes
23. In Vivo Fiber Optic Raman Spectroscopy of Muscle in Preclinical Models of Amyotrophic Lateral Sclerosis and Duchenne Muscular Dystrophy
24. The Lost Tribe: The Importance of Health Care Staff and Service Design During COVID-19
25. Autologous hematopoietic stem cell transplantation following pulsed cyclophosphamide in a severely disabled patient with malignant multiple sclerosis
26. Central axons preparing to myelinate are highly sensitivity to ischemic injury
27. Simultaneous ALS and SCA2 associated with an intermediate-length ATXN2 CAG-repeat expansion
28. Modelling and analysis of electrical impedance myography of the lateral tongue
29. The application of Raman spectroscopy to the diagnosis of mitochondrial muscle disease: A preliminary comparison between fibre optic probe and microscope formats.
30. Vesicular apparatus, including functional calcium channels, are present in developing rodent optic nerve axons and are required for normal node of Ranvier formation
31. Functional glutamate transport in rodent optic nerve axons and glia
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).
36. Correction to: Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease
37. Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease
38. Biomarkers in Motor Neuron Disease: A State of the Art Review
39. Holocord syrinx presenting with foot drop
40. Sleep deprivation and melatonin for inducing sleep in paediatric electroencephalography: a prospective multicentre service evaluation
41. Can neonatal staff site EEG leads in the correct position? A pilot study
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.
45. The Lost Tribe: The Importance of Health Care Staff and Service Design During COVID-19.
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
48. Delayed toxic–hypoxic encephalopathy
49. Autologous hematopoietic stem cell transplantation following pulsed cyclophosphamide in a severely disabled patient with malignant multiple sclerosis
50. Clinician-scientist training: A perspective from across the pond
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