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37 results on '"Conforti, Francesca L"'

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1. Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

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

4. ATXN2 trinucleotide repeat length correlates with risk of ALS

5. TBK1 is associated with ALS and ALS-FTD in Sardinian patients

6. ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion

7. Genetic counselling in ALS: facts, uncertainties and clinical suggestions

8. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis

9. HFE p.H63D polymorphism does not influence ALS phenotype and survival

10. CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

11. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

12. Association Study of the 5′UTR Intron of the FAD2-2 Gene With Oleic and Linoleic Acid Content in Olea europaea L.

13. PACAP and PAC1R are differentially expressed in motor cortex of amyotrophic lateral sclerosis patients and support survival of iPSC-derived motor neurons

15. A Novel Mutation in the Notch3 Gene in an Italian Family With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Genetic and Magnetic Resonance Spectroscopic Findings

16. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

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

18. Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene

19. PACAP and PAC1R are differentially expressed in motor cortex of amyotrophic lateral sclerosis patients and support survival of iPSC-derived motor neurons

21. ATNX2 is not a regulatory gene in Italian ALS patients with C9ORF72 GGGGCC expansion

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

23. ATXN2 trinucleotide repeat length correlates with risk of ALS

24. CHCH10 mutations in an Italian cohort of familial and sporadic ALS patients

25. ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

27. TBK1 is associated with ALS and ALS-FTD in Sardinian patients

28. TBK1 is associated with ALS and ALS-FTD in Sardinian patients

29. Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis

33. Mutation analysis of the MECP2 gene in patients with Rett syndrome

34. Notch3 Gene in an Italian Family With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Genetic and Magnetic Resonance Spectroscopic Findings.

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

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