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25 results on '"Sidle KC"'

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1. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

2. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

3. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

4. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

5. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

6. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

7. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

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

9. Review: Prion-like mechanisms of transactive response DNA binding protein of 43 kDa (TDP-43) in amyotrophic lateral sclerosis (ALS).

10. Executive dysfunction predicts social cognition impairment in amyotrophic lateral sclerosis.

11. Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis.

12. Myasthenia gravis and neuromyelitis opica: A causal link.

13. Molecular classification of sporadic Creutzfeldt-Jakob disease.

14. Molecular screening of sheep for bovine spongiform encephalopathy.

15. The same prion strain causes vCJD and BSE.

16. Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

17. Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.

18. Unaltered susceptibility to BSE in transgenic mice expressing human prion protein.

19. Transmission of fatal familial insomnia to laboratory animals.

20. Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein.

21. Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.

22. Prion protein is necessary for normal synaptic function.

24. Deletions in the prion protein gene are not associated with CJD.

25. Inherited prion disease (PrP lysine 200) in Britain: two case reports.

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