Abstracts (HTML) List of Authors

Carranza, J.

Time to Retreatment after AbobotulinumtoxinA (Dysport) Injections in Children with Dynamic Equinus Foot Deformity
Phase 3 Trial to Evaluate AbobotulinumtoxinA (Dysport) Injections in Children with Upper Limb Spasticity Due to Cerebral Palsy: A Study Design

Cattani, A.

What Is the Right Pressure of Shunt Valves in Newborns?

Catus, F.

Phase 3 Trial to Evaluate AbobotulinumtoxinA (Dysport) Injections in Children with Upper Limb Spasticity Due to Cerebral Palsy: A Study Design

Chao, M. M.

Transcobalamin II Deficiency: Rare Differential Diagnosis in a Neonate with Hematological Disease and Failure to Thrive

Chiriboga, C. A.

Interim Efficacy and Safety Results from the Phase 3 ENDEAR Study of Nusinersen in Infants Diagnosed with Spinal Muscular Atrophy (SMA)

Chiriboga, Claudia A.

Efficacy and safety of nusinersen in children with later-onset spinal muscular atrophy (SMA): results of the phase 3 CHERISH study

Choe, C. U.

Distinct Regulation of Orexigenic and Anorexigenic Hypothalamic Pathways in Creatine-Deficient Mice

Christ, S.

Severe Course of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) with Detection of an Unknown Antineuronal Antibody

Christen, H.-J.

Acute Flaccid Paralysis of Unknown Cause: A Report of Three Unusual Cases Mimicking Poliomyelitis

Cloppenborg, T.

Dramatic Onset of Focal Seizures: Differentiating Structural Focal Epilepsy from Ring Chromosome 20

Coci, E. G.

Novel Homozygous Missense Mutation in ALDH7A1 Causes Neonatal Pyridoxine-Dependent Epilepsy
Unbalanced Translocation Affecting the Long Arms of Chromosome 10 and 22 Causes Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy

Codutti, L.

Novel Homozygous Missense Mutation in ALDH7A1 Causes Neonatal Pyridoxine-Dependent Epilepsy

Cohen-Pfeffer, J. L.

Expert Opinion on the Management of Intracerebroventricular (ICV) Drug Delivery

Coras, R.

Histopathological Proof of the Pathogenetic Role of a Rare GFAP Mutation in Alexander´s Disease with Isolated Flaccid Paraparesis

Cordey, A.

Explorative Saccade Training in Children with Homonymous Hemianopia

Costard, S.

Difficulties in the Acquisition of Literacy in Children with Rolandic Epilepsy or Rolandic EEG Pattern

Curatolo, P.

Predictors of Efficacy in Patients with Adjunctive Everolimus Therapy for Treatment-Resistant Seizures Associated with Tuberous Sclerosis Complex