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Your search keyword '"Steyn, Frederik J"' showing total 25 results

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25 results on '"Steyn, Frederik J"'

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1. Characterization of the skeletal muscle arginine methylome in health and disease reveals remodeling in amyotrophic lateral sclerosis

2. Impaired signaling for neuromuscular synaptic maintenance is a feature of Motor Neuron Disease

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

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

5. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1.

6. Patient perspectives on digital healthcare technology in care and clinical trials for motor neuron disease: an international survey

7. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

8. Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

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

10. Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

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

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

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

14. Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

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

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

17. A Road Map for Remote Digital Health Technology for Motor Neuron Disease

18. Venous creatinine as a biomarker for loss of fat-free mass and disease progression in patients with Amyotrophic Lateral Sclerosis

19. Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

20. Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

24. Loss of appetite is associated with a loss of weight and fat mass in patients with amyotrophic lateral sclerosis

25. Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

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