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1. Ice crystal classification using two dimensional light scattering patterns

2. COORDINATED AIRBORNE STUDIES IN THE TROPICS (CAST)

4. Association of CAG Repeats With Long-term Progression in Huntington Disease

5. The apolipoprotein E [epsilon]4 allele selectively increases the risk of frontotemporal lobar degeneration in males

6. Identification of symbol digit modality test score extremes in Huntington's disease

7. Apathy associated with impaired recognition of happy facial expressions in Huntington's disease

10. MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1

11. Suicidal ideation in a European Huntington's disease population

12. Co-ordinated Airborne Studies in the Tropics (CAST)

13. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

14. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

15. The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients

17. Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY

18. NMDA receptor gene variations as modifiers in Huntington disease: a replication study

19. Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

20. Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

22. β-Defensin Genomic Copy Number Does Not Influence the Age of Onset in Huntington's Disease

23. Discrepancies in reporting the CAG repeat lengths for Huntington's disease

24. NMDA receptor gene variations as modifiers in Huntington disease

26. Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

29. Apolipoprotein E epsilon 4 allele frequency and age at onset of Alzheimer's disease.

30. The apolipoprotein E £4 allele selectively increases the risk of frontotemporal lobar degeneration in males.

31. Genetic associations between cathepsin D exon 2 C-->T polymorphism and Alzheimer's disease, and pathological correlations with genotype.

32. 3-Deazaadenosine-induced disorganization of macrophage microfilaments.

33. Antagonism by taxol of effects of microtubule-disrupting agents on lymphocyte cAMP metabolism and cell function.

40. Identification of genetic variants associated with Huntington's disease progression

41. Genetic testing in motor neuron disease and frontotemporal dementia: a 5-year multicentre evaluation.

42. The PopN Gate-keeper Complex Acts on the ATPase PscN to Regulate the T3SS Secretion Switch from Early to Middle Substrates in Pseudomonas aeruginosa.

43. Improving follow up after predictive testing in Huntington's disease: evaluating a genetic counselling narrative group session.

44. Genetic Counselling and Narrative Practices: A Model of Support following a "Negative" Predictive Test for Huntington's Disease.

45. Reliability and factor structure of the Short Problem Behaviors Assessment for Huntington's disease (PBA-s) in the TRACK-HD and REGISTRY studies.

46. Modulation of the cGAS-STING DNA sensing pathway by gammaherpesviruses.

47. Neuropsychiatry and White Matter Microstructure in Huntington's Disease.

48. Real-time detection of airborne asbestos by light scattering from magnetically re-aligned fibers.

49. The pediatric preclinical testing program: description of models and early testing results.

50. Apolipoprotein E epsilon4 allele frequency and age at onset of Alzheimer's disease.

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