Elisa De Grandis

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 423 citations · Full text

Life Sciences, Genetics, Neurology +9

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 · 157 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Long-Term Follow-Up of Neuroblastoma-Associated Opsoclonus-Myoclonus-Ataxia Syndrome

Elisa De Grandis, Stefano Parodi, Massimo Conte et al. · Neuropediatrics · 2009 · 94 citations

Medicine, Neurology, Pediatrics +15

Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome

Shereen G. Ghosh, Kerstin Becker, He Huang et al. · The American Journal of Human Genetics · 2018 · 89 citations · Full text

Life Sciences, Molecular Genetics, Neuroscience +14

Cerebral Folate Deficiency Syndromes in Childhood

Belén Pérez‐Dueñas, Aída Ormazábal, Claudio Toma et al. · Archives of Neurology · 2011 · 67 citations

Life Sciences, Neurology, Neuroscience +17