Search

Your search keyword '"Taroni, F."' showing total 1,174 results

Search Constraints

Start Over You searched for: Author "Taroni, F." Remove constraint Author: "Taroni, F."
1,174 results on '"Taroni, F."'

Search Results

4. Chronic cholesterol administration to the brain supports complete and long-lasting cognitive and motor amelioration in Huntington's disease

9. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

10. Clinical and genetic characteristics of Dent's disease type 1 in Europe.

11. Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias.

23. Hypomyelinating leukodystrophies in adults: Clinical and genetic features

24. Insights into kinetics, release, and behavioral effects of brain-targeted hybrid nanoparticles for cholesterol delivery in Huntington's disease

26. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

29. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

30. Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study

31. Multifaceted and Age-Dependent Phenotypes Associated With Biallelic PNPLA6 Gene Variants: Eight Novel Cases and Review of the Literature

37. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

38. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

39. Bayes Factors for Forensic Decision Analyses with R

40. The Bayes' factor: the coherent measure for hypothesis confirmation

46. Neuropsychological features of adult form of Alexander disease

47. Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (Nature Genetics, (2020), 52, 5, (473-481), 10.1038/s41588-020-0615-4)

50. Risk factors for gallstone disease: the Sirmione study

Catalog

Books, media, physical & digital resources