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Melania Giannotta | doi.page

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Melania Giannotta

Institute of Neurological Sciences(IT)Istituto delle Scienze Neurologiche di Bologna(IT)

Publications by Year

Research Areas

Genomics and Rare Diseases, Neurogenetic and Muscular Disorders Research, Hereditary Neurological Disorders, Muscle Physiology and Disorders, Epilepsy research and treatment

Most-Cited Works

→ De novo mutations in ATP1A3 cause alternating hemiplegia of childhood(2012)418 cited
→ Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients(2015)153 cited
→ Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults(2010)143 cited
→ Intrathecal methotrexate affects cognitive function in children with medulloblastoma(2002)117 cited
→ Neuropsychological development in children belonging to BECTS spectrum: Long-term effect of epileptiform activity(2013)76 cited
→ Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients(2017)47 cited

→ Onasemnogene abeparvovec in spinal muscular atrophy: predictors of efficacy and safety in naïve patients with spinal muscular atrophy and following switch from other therapies(2023)

41 cited

→ Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults(2017)35 cited

→ Comparing cortical auditory processing in children with typical and atypical benign epilepsy with centrotemporal spikes: Electrophysiologic evidence of the role of non–rapid eye movement sleep abnormalities(2015)28 cited

→ Alternating hemiplegia of childhood: Metabolic studies in the largest European series of patients(2011)26 cited