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28 results on '"Andersen, Peter M"'

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1. Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers

2. Quality of life and depression in patients with amyotrophic lateral sclerosis – does the country of origin matter?

3. Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

4. The impact of age on genetic testing decisions in amyotrophic lateral sclerosis

6. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

7. Additional file 1 of Peripheral administration of SOD1 aggregates does not transmit pathogenic aggregation to the CNS of SOD1 transgenic mice

8. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

9. Gut microbiota-specific IgA+ B cells traffic to the CNS in active multiple sclerosis

10. Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

11. Putative founder effect in the Polish, Iranian and United States populations for the L144S SOD1 mutation associated with slowly uniform phenotype of amyotrophic lateral sclerosis

12. Additional file 1 of Aggregate-selective antibody attenuates seeded aggregation but not spontaneously evolving disease in SOD1 ALS model mice

13. Different neuroinflammatory profile in amyotrophic lateral sclerosis and frontotemporal dementia is linked to the clinical phase

14. Comprehensive analysis of the mutation spectrum in 301 German ALS families

15. Hot-spot KIF5A mutations cause familial ALS

16. Pyrimethamine Significantly Lowers Cerebrospinal Fluid Cu/Zn Superoxide Dismutase in Amyotrophic Lateral Sclerosis Patients with SOD1 Mutations

17. Truncating mutations in FUS/TLS give rise to a more aggressive ALS-phenotype than missense mutations: A clinico-genetic study in Germany

18. A 50 bp deletion in the SOD1 promoter lowers enzyme expression but is not associated with ALS in Sweden

20. Multicenter Validation Of Csf Neurofilaments As Diagnostic Biomarkers For Als

21. C9orf72 and UNC13A are shared risk loci for ALS and FTD: a genome-wide meta-analysis

22. No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

23. Physical activity and risk of Amyotrophic Lateral Sclerosis in a prospective cohort study

24. Smoking and Risk for Amyotrophic Lateral Sclerosis: Analysis of the EPIC Cohort

25. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

26. Hot-spot KIF5A mutations cause familial ALS

27. The effect of SMN gene dosage on ALS risk and disease severity

28. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

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