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JOURNAL OF CHILD NEUROLOGY
Rivista
Codice:
E090932
ISSN:
0883-0738
Dati Generali
Dati Generali
Pubblicazioni (33)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A New Self-Report Quality of Life Questionnaire for Children With Neuromuscular Disorders: Presentation of the Instrument, Rationale for Its Development, and Some Preliminary Results
Articolo
Add-on lamotrigine treatment in children and young adults with severe partial epilepsy: a open, prospective, long-term study
Articolo
Atypical Manifestations in Glut1 Deficiency Syndrome
Articolo
Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case.
Articolo
Cerebellum enlargement and corpus callosum agenesis: a longitudinal case report.
Articolo
Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients with Agenesis of the Corpus Callosum
Articolo
Cognitive profiles and visuoperceptual abilities in preterm and term spastic diplegic children with periventricular leukomalacia.
Articolo
Complementary and Alternative…but Please Not Secret
Articolo
Developmental Outcomes of Aicardi Goutières Syndrome
Articolo
Different mutations in three prime repair exonuclease 1 and ribonuclease H2 genes affect clinical features in Aicardi-Goutieres syndrome
Articolo
Early-Onset Aicardi-Goutières Syndrome: Magnetic Resonance Imaging (MRI) Pattern Recognition
Articolo
Early-onset occipital idiopathic epilepsy: a syndrome to be treated?
Articolo
Electrophysiologic study of central motor pathways in ataxia-telangiectasia.
Articolo
Factors predicting the efficacy of botulinum toxin-A treatment of the lower limb in children with cerebral palsy
Articolo
MCT8 deficiency: extrapyramidal symptoms and delayed myelination as prominent features.
Articolo
MCT8 deficiency: extrapyramidal symptoms and delayed myelination as prominent features.
Articolo
Mitochondrial DNA deletion in a child with mitochondrial encephalomyopathy, growth hormone deficiency, and hypoparathyroidism.
Articolo
Mother-Child Agreement on Behavioral Ratings in Tourette Syndrome: A Controlled Study.
Articolo
Parent and self-report health-related quality of life measures in young patients with Tourette syndrome.
Articolo
Parent and self-report health-related quality of life measures in young patients with tourette syndrome
Articolo
Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome
Articolo
Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15
Articolo
Reaching and writing movements: Sensitive and reliable tools to measure genetic dystonia in children
Articolo
Response to correspondence on "spinal cord calcification in an early-onset progressive leukoencephalopathy"
Articolo
SECHEL SYNDROME AND MALFORMATIONS OF CORTICAL DEVELOPMENT REPORT OF THREE NEW CASES AND REVIEW OF THE LITERATURE
Articolo
Seckel's syndrome and malformations of cortical development: Report of three new cases and review of the literature
Articolo
Spectrum of visual disorders in children with cerebral visual impairment.
Articolo
Speed-Accuracy Trade-Off in a Trajectory-Constrained Self-Feeding Task: A Quantitative Index of Unsuppressed Motor Noise in Children With Dystonia
Articolo
Spinal cord calcification in an early-onset progressive leukoencephalopathy.
Articolo
Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance Test.
Articolo
Subependymal periventricular heterotopias in a patient with ehlers-danlos syndrome: a new case
Articolo
The Diagnostic Yield of Array Comparative Genomic Hybridization Is High Regardless of Severity of Intellectual Disability/Developmental Delay in Children
Articolo
Unilateral periventricular nodular heterotopia associated with diffuse areas of cerebral functional abnormalities
Articolo
No Results Found
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