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You searched for: Author/Creator Vaula, Giovanna

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1. A novel homozygous change of CLCN2 (p.His590Pro) is associated with a subclinical form of leukoencephalopathy with ataxia (LKPAT). Issue 10 (4th May 2017)

2. Analysis of LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele‐Specific Expression. Issue 1 (28th October 2013)

3. Analysis of LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele‐Specific Expression. Issue 8 (28th May 2013)

4. Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38). (July 2016)

5. Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38). (July 2016)

6. COVID-19 Severity in Multiple Sclerosis: Putting Data Into Context. Issue 1 (January 2022)

7. Heterozygous NOTCH1 Variants Cause CNS Immune Activation and Microangiopathy. Issue 5 (20th August 2022)