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You searched for: Author/Creator Balestrini, Simona

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2. Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study. (24th November 2020)

3. Cerebellar, limbic, and midbrain volume alterations in sudden unexpected death in epilepsy. (14th March 2019)

4. Clinical spectrum of STX1B-related epileptic disorders. (12th March 2019)

5. Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy. Issue 3 (4th July 2019)

6. De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy. Issue 12 (29th June 2016)

7. Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences. (3rd May 2022)

8. Expanding the genetic and phenotypic spectrum of CHD2‐related disease: From early neurodevelopmental disorders to adult‐onset epilepsy. Issue 2 (29th October 2021)

9. Genome‐wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug‐resistant epilepsy. (16th July 2018)

10. Increased Common Carotid Artery Wall Thickness Is Associated with Rapid Progression of Asymptomatic Carotid Stenosis. Issue 5 (25th November 2013)