Livia Pisciotta

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 · 85 citations · Full text

Biallelic Mutations, Genetic Disorder, Encoding Adp-ribosylhydrolase 3 +5

Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients

Livia Pisciotta, Marcella Gherzi, Michela Stagnaro et al. · Brain and Development · 2017 · 46 citations · Full text

Pediatric Hematology, Hematology, Pediatrics +5

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

CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations

Andrea Accogli, Marcello Scala, Annalisa Calcagno et al. · European Journal of Medical Genetics · 2018 · 31 citations

Neurobiology Of Disease, Cnnm2 Homozygous Mutations, Mendelian Disorder +11

Combined early treatment in hemiplegic attacks related to CACNA1A encephalopathy with brain oedema: Blocking the cascade?

Francesca Camia, Livia Pisciotta, Giovanni Morana et al. · Cephalalgia · 2016 · 29 citations

Neurological Disorder, Brain Lesion, Epilepsy +22