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21. Familial periventricular nodular heterotopia, epilepsy and Melnick–Needles Syndrome caused by a single FLNA mutation with combined gain-of-function and loss-of-function effects. Issue 6 (9th March 2015)

23. Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy. (December 2016)

25. Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures. (29th May 2020)

26. Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies. (13th September 2016)

27. Pitfalls in genetic testing: the story of missed SCN1A mutations. Issue 4 (14th April 2016)

28. Quantitative MRI-Based Analysis Identifies Developmental Limbic Abnormalities in PCDH19 Encephalopathy. (25th June 2020)

29. Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies. Issue 10 (26th April 2021)

30. Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects. Issue 4 (22nd March 2017)