Pubblicazioni

Cyclic alternating pattern in infants with congenital hypothyroidism

2019 - BRAIN & DEVELOPMENT

Santana-Miranda, Rafael; Murata, Chiharu; Bruni, Oliviero; Rosa, Agostinho; Alvarado Ruiz, Gerardo Alberto; Castillo Montoya, Carlos RaÃºl; Rojas-Zamorano, JosÃ© Ãngel; Esqueda-LeÃ³n, Enrique; Dominguez-Salazar, Emilio; Poblano, Adrian; Velazquez-Moctezuma, Javier

KCNQ2 encephalopathy: A case due to a de novo deletion

2018 - BRAIN & DEVELOPMENT

Spagnoli, C.; Salerno, G. G.; Iodice, A.; Frattini, D.; Pisani, F.; Fusco, C.

A novel temporal pattern of childhood cerebral X-linked adrenoleukodystrophy

2018 - BRAIN & DEVELOPMENT

Turco, E. C.; Ormitti, F.; Andreolli, A.; Barsacchi, M.; Facini, C.; Pisani, F.

Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1

2017 - BRAIN & DEVELOPMENT

Travaglini, Lorena; Aiello, Chiara; Alesi, Viola; Loddo, Sara; Novelli, Antonio; Tozzi, Giulia; Bertini, Enrico; Leuzzi, Vincenzo; Brancati, Francesco

Remarks about âa pediatric patient of hemorrhagic acute transverse myelitisâ

2017 - BRAIN & DEVELOPMENT

Coraci, Daniele; Santilli, Valter; Giovannini, Silvia; Padua, Luca

Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis

2017 - BRAIN & DEVELOPMENT

Iodice, A.; Spagnoli, C.; Salerno, G. G.; Frattini, D.; Bertani, G.; Bergonzini, P.; Pisani, F.; Fusco, C.

Letter to the Editor

2016 - BRAIN & DEVELOPMENT

Pisani, F.; Piccolo, B.; Cantalupo, G.; Copioli, C.; Fusco, C.; Pelosi, A.; Tassinari, C. A.; Seri, S.

Hereditary Hemorrhagic Telangiectasia presenting as migraine: A case report

2015 - BRAIN & DEVELOPMENT

Facini, C.; Pavlidis, E.; Turco, E. C.; Pisani, F.

Paroxysmal nonepileptic motor phenomena in newborn

2015 - BRAIN & DEVELOPMENT

Orivoli, S.; Facini, C.; Pisani, F.