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Your search keyword '"Yevgeniya Abramzon"' showing total 18 results

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18 results on '"Yevgeniya Abramzon"'

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1. Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types

2. Pathogenic huntingtin repeat expansions in patients with frontotemporal dementia and amyotrophic lateral sclerosis

3. Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types

4. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture

5. The Overlapping Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

6. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

7. Mutations in the SPTLC1 gene are a cause of juvenile amyotrophic lateral sclerosis that may be amenable to serine supplementation

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

9. Genetic analysis of neurodegenerative diseases in a pathology cohort

10. To Dement or Not to Dement, That Is the Question

11. Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease

12. A genome-wide association study of myasthenia gravis

13. Large C9orf72 repeat expansions are not a common cause of Parkinson’s disease

14. Repeat expansion in C9ORF72 in Alzheimer's disease

15. FUS mutations in sporadic amyotrophic lateral sclerosis

16. A de novo missense mutation of the FUS gene in a 'true' sporadic ALS case

17. Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis

18. C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

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