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

4. Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

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

9. The clinical spectrum of CASQ1-related myopathy

11. Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in ‘FUSDelta14’ knockin mice

12. Severe trichothiodystrophy and cardiac malformation in a newborn carrying a novel GTF2H5 homozygous truncating variant.

13. TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations

14. Preliminary design and validation of the '6-K-scale' for bulbar symptoms evaluation in SBMA

15. Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

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

17. Specific heterozygous frameshift variants in hnRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

21. Brain White Matter MRI Differentiates Kennedy’s Disease from Other Motor Neuron Disease Clinical Phenotypes (P4.4-011)

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

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

25. Non-neural phenotype of spinal and bulbar muscular atrophy: Results from a large cohort of Italian patients

26. No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype

27. Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS

29. PORPHYRIA REGISTRY PADOVA -- START UP.

30. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

31. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

32. Structural Brain MRI Abnormalities in Kennedy's Disease (P5.015)

34. The clinical spectrum of -related myopathy.

36. Non-neural phenotype of spinal and bulbar muscular atrophy: results from a large cohort of Italian patients

37. The wide clinical phenotype of Kennedy’s disease. (P7.055)

45. Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS

46. Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia

49. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

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