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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. Traceability of 'Tuscan PGI' Extra Virgin Olive Oils by ¹H NMR Metabolic Profiles Collection and Analysis

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

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

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

8. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

9. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

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

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

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

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

16. Gene conversion events in adult-onset spinal muscular atrophy

18. Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia

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

20. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

24. A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1

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

43. Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)

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