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20 results on '"Fontaine B"'

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1. Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

2. Differential default mode network trajectories in asymptomatic individuals at risk for Alzheimer's disease

3. Awareness of cognitive decline trajectories in asymptomatic individuals at risk for AD

4. Association of cerebrospinal fluid α-synuclein with total and phospho-tau181 protein concentrations and brain amyloid load in cognitively normal subjective memory complainers stratified by Alzheimer's disease biomarkers

5. Gray Matter Network Disruptions and Regional Amyloid Beta in Cognitively Normal Adults

6. Validation of the French version of the Hospital Survey on Patient Safety Culture questionnaire

7. MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

8. Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients

9. De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

10. Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles

11. The Genetic Association of Variants in CD6, TNFRSF1A and IRF8 to Multiple Sclerosis: A Multicenter Case-Control Study

12. Phase II multicenter study of epirubicin for hormone-resistant prostatic cancer with measurable soft tissue disease

14. Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

15. Comparative effectiveness of teriflunomide vs dimethyl fumarate in multiple sclerosis

16. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

17. Power estimation for non-standardized multisite studies

18. Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease

19. Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

20. ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependence

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