Daniele Frattini

<i>HCN1</i>mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond

Carla Marini, Alessandro Porro, Agnès Rastetter et al. · Brain · 2018 · 134 citations · Full text

The ring 14 syndrome: Clinical and molecular definition

Marcella Zollino, Laura Seminara, Daniela Orteschi et al. · American Journal of Medical Genetics Part A · 2009 · 58 citations

<i>UFM1</i> founder mutation in the Roma population causes recessive variant of H-ABC

Eline M. Hamilton, Enrico Bertini, Luba Kalaydjieva et al. · Neurology · 2017 · 55 citations · Full text

Acute and chronic corticosteroid treatment of ten patients with paralytic form of Sydenham’s chorea

Carlo Fusco, Valentina Ucchino, Daniele Frattini et al. · European Journal of Paediatric Neurology · 2011 · 35 citations

Chronic Corticosteroid Treatment, Paralytic Form, Neurology +2

Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation

Carlo Fusco, Daniele Frattini, Enrico Farnetti et al. · Brain and Development · 2009 · 29 citations

Rare Diseases, Spinal Cord Injury, Neurological Disorder +11