Michela Stagnaro
Istituto Giannina Gaslini(IT)
Publications by Year
Research Areas
Neurogenetic and Muscular Disorders Research, Genomics and Rare Diseases, Hereditary Neurological Disorders, Ion Transport and Channel Regulation, Metabolism and Genetic Disorders
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
- → Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients(2017)47 cited
- → Cardiac phenotype in ATP1A3 -related syndromes(2020)43 cited
- → Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype(2015)41 cited
- → Identification of a rare 17p13.3 duplication including the BHLHA9 and YWHAEgenes in a family with developmental delay and behavioural problems(2012)40 cited
- → Alternating Hemiplegia of Childhood: Genotype–Phenotype Correlations in a Cohort of 39 Italian Patients(2021)23 cited
- → Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism(2014)17 cited
- → ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases(2018)15 cited
- → White matter and cerebellar involvement in alternating hemiplegia of childhood(2020)12 cited