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Neuropediatrics|November 19, 2010
Gastric dysmotility following orthopaedic scoliosis surgery in patients with cerebral palsy: a case seriesS Vande Velde, S Van Biervliet, R De Bruyne, et al.
Neuropediatrics|September 23, 2010
Cardio-facio-cutaneous syndrome: phenotypic variability and differential diagnosis in 3 cases with de novo BRAF mutationsE Demir, G Mancano, M G Pomponi, et al.
Neuropediatrics|September 23, 2010
A new nonsense mutation of the IGHMBP2 gene responsible for the first case of SMARD1 in a Sardinian patient with giant cell hepatitisVassilios Fanos, A Cuccu, S Nemolato, et al.
Neuropediatrics|September 23, 2010
The relationship of seizure activity and chronic epilepsy in early infancy and short-term neurodevelopmental outcome following fetal myelomeningocele closureE Danzer, R Finkel, M Gerdes, et al.
Neuropediatrics|August 1, 1991
Neuroradiological findings in Sturge-Weber syndrome (SWS) and isolated pial angiomatosisP Terdjman, J Aicardi, C Sainte-Rose, et al.
Neuropediatrics|August 1, 1991
Transcranial Doppler evaluation of cerebral infarction in the neonateJ Messer, J Haddad, R Casanova
Neuropediatrics|May 7, 2010
Effect of multiple cranial burr hole surgery on prevention of recurrent ischemic attacks in children with moyamoya diseaseR S de Oliveira, M C M Amato, G N Simão, et al.
Neuropediatrics|May 7, 2010
Massive hemobilia and papillomatosis of the gallbladder in metachromatic leukodystrophy: a life-threatening conditionL Garavelli, S Rosato, A Mele, et al.
Neuropediatrics|May 7, 2010
Enhancing cranial nerves and cauda equina: an emerging magnetic resonance imaging pattern in metachromatic leukodystrophy and krabbe diseaseG Morana, R Biancheri, M Dirocco, et al.
Neuropediatrics|July 2, 2009
Genetic polymorphism and idiopathic generalized epilepsy. Evidence of interaction between haptoglobin and ACP1 systemsF Gloria-Bottini, P Lucarelli, P Saccucci, et al.
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