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1. Abnormal molecular signatures of inflammation, energy metabolism, and vesicle biology in human Huntington disease peripheral tissues.

2. Quantification of huntingtin protein species in Huntington's disease patient leukocytes using optimised electrochemiluminescence immunoassays.

3. Loss of extra-striatal phosphodiesterase 10A expression in early premanifest Huntington's disease gene carriers.

4. Short-interval observational data to inform clinical trial design in Huntington's disease.

5. Altered PDE10A expression detectable early before symptomatic onset in Huntington's disease.

6. Quantification of mutant huntingtin protein in cerebrospinal fluid from Huntington's disease patients.

7. An exploratory double-blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington's disease.

8. Analysis of White Adipose Tissue Gene Expression Reveals CREB1 Pathway Altered in Huntington's Disease.

9. Cerebellar abnormalities in Huntington's disease: a role in motor and psychiatric impairment?

10. Biomarker development for Huntington's disease.

11. Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression.

12. Clinical and genetic characteristics of late-onset Huntington's disease

13. Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study

14. Cognitive decline in Huntington's disease expansion gene carriers

15. Task-Specific Training in Huntington Disease: A Randomized Controlled Feasibility Trial

16. An exploratory double-blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington’s disease

17. Altered PDE10A expression detectable early before symptomatic onset in Huntington's disease.

18. Development of an ELISA assay for the quantification of soluble huntingtin in human blood cells.

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

20. Clinical manifestations of intermediate allele carriers in Huntington disease

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