Works matching IS 08830738 AND DT 2013 AND VI 28 AND IP 3
Results: 22
JCN Calendar of Events.
- Published in:
- 2013
- Publication type:
- Calendar
The Journal of Child Neurology: 28 Years and Still Improving.
- Published in:
- 2013
- By:
- Publication type:
- Editorial
Views of Recently First-Certified US Child Neurologists on Their Residency Training.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 332, doi. 10.1177/0883073812473644
- By:
- Publication type:
- Article
Pediatric Herpes Simplex Virus Encephalitis: A Retrospective Multicenter Experience.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 321, doi. 10.1177/0883073812471428
- By:
- Publication type:
- Article
Pharmacological Treatment of Neonatal Seizures: A Systematic Review.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 351, doi. 10.1177/0883073812470734
- By:
- Publication type:
- Article
Jean Aicardi: My Circuitous Path to Becoming a French Child Neurologist and Epileptologist.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 409, doi. 10.1177/0883073812470212
- By:
- Publication type:
- Article
Mitochondrial Depletion Causes Neonatal-Onset Leigh Syndrome, Myopathy, and Renal Tubulopathy.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 404, doi. 10.1177/0883073812469722
- By:
- Publication type:
- Article
Torticollis.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 365, doi. 10.1177/0883073812469294
- By:
- Publication type:
- Article
Response to Correspondence on “Active Comparator-Controlled, Rater-Blinded Study of Corticotropin-Based Immunotherapies for Opsoclonus-Myoclonus Syndrome”.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Conventional Versus Multimodal Corticotropin-Based Immunotherapies for Opsoclonus-Myoclonus Syndrome: Where Are We?
- Published in:
- 2013
- By:
- Publication type:
- Letter
Anticonvulsant Medication Errors in Children With Epilepsy During the Home-to-Hospital Transition.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 314, doi. 10.1177/0883073812446632
- By:
- Publication type:
- Article
Vigabatrin and Mental Retardation in Tuberous Sclerosis: Infantile Spasms Versus Focal Seizures.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 308, doi. 10.1177/0883073812446485
- By:
- Publication type:
- Article
Height Assessments in Children With Neurofibromatosis Type 1.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 303, doi. 10.1177/0883073812446310
- By:
- Publication type:
- Article
Prevalence of Seizures in Children Infected With Human Immunodeficiency Virus.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 297, doi. 10.1177/0883073812446161
- By:
- Publication type:
- Article
Seizures as the Clinical Presenting Symptom in Children with Brain Tumors.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 292, doi. 10.1177/0883073812445786
- By:
- Publication type:
- Article
Primary Supratentorial Atypical Teratoid/Rhabdoid Tumor in Children: A Report of Two Cases.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Infantile-Onset Alexander Disease: A Genetically Proven Case With Mild Clinical Course in a 6-Year-Old Indian Boy.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 396, doi. 10.1177/0883073812444313
- By:
- Publication type:
- Article
Dystonia in Childhood: Clinical and Objective Measures and Functional Implications.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 340, doi. 10.1177/0883073812444312
- By:
- Publication type:
- Article
Angelman Syndrome Due to a Termination Codon Mutation of the UBE3A Gene.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 392, doi. 10.1177/0883073812443591
- By:
- Publication type:
- Article
SCN1A Mutation Associated With Intractable Myoclonic Epilepsy and Migraine Headache.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 389, doi. 10.1177/0883073812443309
- By:
- Publication type:
- Article
Clinical Features and Ryanodine Receptor Type 1 Gene Mutation Analysis in a Chinese Family With Central Core Disease.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 384, doi. 10.1177/0883073812441251
- By:
- Publication type:
- Article
The Very Low Density Lipoprotein Receptor–Associated Pontocerebellar Hypoplasia and Dysmorphic Features in Three Turkish Patients.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 3, p. 379, doi. 10.1177/0883073812441065
- By:
- Publication type:
- Article