113 results on '"Talbot K"'
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2. Comfort perception of 3D printed orthotics in individuals with symptomatic pes planus
3. Measuring coping in people with amyotrophic lateral sclerosis using the Coping Index-ALS: A patient derived, Rasch compliant scale
4. Corrigendum to: Tie2-dependent knockout of HIF-1 impairs burn wound vascularization and homing of bone marrow-derived angiogenic cells
5. Dysbindin-1 and Its Protein Family
6. An Unusual Presentation of Pneumocystis Jirovecii Pneumonia Presenting as Multiples Masses and Nodules
7. Profiling Manufacturing Organisations — A Comparison of Four Different Methods
8. The sensory and affective components of pain: are they differentially modifiable dimensions or inseparable aspects of a unitary experience? A systematic review
9. Rivaroxaban and apixaban induce clotting factor Xa fibrinolytic activity
10. The two-year progression of structural and functional cerebral MRI in amyotrophic lateral sclerosis
11. Epigenetic signatures and early detection of neurodegenerative diseases: Development of stratifying biomarkers for amyotrophic lateral sclerosis in Asian cohorts
12. The clinical landscape for SMA in a new therapeutic era
13. The SMA Trust: the role of a disease-focused research charity in developing treatments for SMA
14. International outbreak of multiple Salmonella serotype infections linked to sprouted chia seed powder – USA and Canada, 2013–2014
15. Trk receptor signalling and sensory neuron fate are perturbed in human neuropathy caused by Gars mutations
16. C9ORF72 and RAB7L1 regulate vesicle traffi cking in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
17. Thrombolysis by chemically modified coagulation factor Xa
18. Development of LNA gapmer oligonucleotide based therapy for FTD/ALS caused by the C9orf72 repeat expansion
19. Modelling amyotrophic lateral sclerosis (ALS) using mutant and CAS9/CRISPR-corrected motor neurons from patients with C9ORF72 mutations reveals disease-specific cellular phenotypes
20. Motor neuron disease: current management and future prospects
21. Neurofilament light chain: A prognostic biomarker in amyotrophic lateral sclerosis
22. TARDBP pathogenic mutations increase cytoplasmic translocation of TDP-43 and cause reduction of endoplasmic reticulum Ca2+ signaling in motor neurons
23. Src kinase as a mediator of convergent molecular abnormalities leading to NMDAR hypoactivity in schizophrenia
24. Deutliche Progression der Schädigung der grauen Substanz bei konstanten Befunden in der weißen Substanz im Krankheitsverlauf der Amyotrophen Lateralsklerose: Eine longitudinale MRT-Studie
25. Neuromuscular junction maturation defects precede impaired lower motor neuron connectivity in Charcot-Marie-Tooth type 2D mice
26. Expanding the genetics of huntingtonism
27. Progressive hemiparesis (Mills syndrome) with aphasia in amyotrophic lateral sclerosis
28. REM sleep behaviour disorder is associated with worse quality of life and other non-motor features in early Parkinson's disease
29. Autoimmune disease preceding amyotrophic lateral sclerosis: An epidemiologic study
30. Should all patients with ALS have genetic testing?
31. A central role of plasmin in cardiac injury initiated by fetal exposure to maternal anti-Ro autoantibodies
32. VMAT1 deletion causes neuronal loss in the hippocampus and neurocognitive deficits in spatial discrimination
33. Whole-brain magnetic resonance spectroscopic imaging measures are related to disability in ALS
34. Coagulation factor X Arg386 specifically affects activation by the intrinsic pathway: a novel patient mutation
35. P29.07: Systematic review of methodology used in ultrasound studies aimed at creating charts of fetal size
36. Systematic review of methodology used in ultrasound studies aimed at creating charts of fetal size
37. RREB1 repressed miR-143/145 modulates KRAS signaling through downregulation of multiple targets
38. A calm before the exome storm: Coming together of dSMA and CMT2
39. 1118 Are MND patients pre-morbidly fitter? Indirect evidence from hospital record-linkage
40. 169 Antisaccade task as a biomarker in MND
41. Familial versus sporadic amyotrophic lateral sclerosis--a false dichotomy?
42. S.I.2 Motor neuron disorders and vulnerability to RNA processing
43. 063 Acceleration of fibrinolysis by factor xa-antithrombin complex
44. Catastrophic hyperkalaemia following administration of suxamethonium chloride to a patient with undiagnosed amyotrophic lateral sclerosis
45. O16 Mouse models of SMA: implications for the timing and delivery of therapy
46. Heterotopic pregnancy
47. Do twin studies still have anything to teach us about the genetics of amyotrophic lateral sclerosis?
48. Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosis
49. POMD09 Understanding the early pathological pathways in Parkinson's disease. The Oxford Parkinson's Disease Centre
50. PATH44 Corpus callosum diffusion tensor imaging as a biomarker for motor neurone disease
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