Rosaria Vavassori

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 417 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +8

Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients

Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro et al. · Orphanet Journal of Rare Diseases · 2015 · 152 citations · Full text

Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults

Eleni Panagiotakaki, Giuseppe Gobbi, Brian Neville et al. · Brain · 2010 · 142 citations · Full text

Neurological Disorder, Education, Cerebral Palsy +19

Biobanking from the patient perspective

Derick Mitchell, Alison Parry-Jones, Hans Keulen et al. · Research Involvement and Engagement · 2015 · 80 citations · Full text

Cardiac phenotype in <i>ATP1A3</i> -related syndromes

Simona Balestrini, Mohamad A. Mikati, Reyes Álvarez‐García‐Rovés et al. · Neurology · 2020 · 43 citations · Full text