Pediatric Neurology

Journal

Publication Venue For

  • Tuberous Sclerosis Complex Genotypes and Developmental Phenotype.  96:58-63. 2019
  • Volumetric Analysis of the Basal Ganglia and Cerebellar Structures in Patients with Phelan-McDermid Syndrome.  90:37-43. 2019
  • A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome.  76:37-46. 2017
  • Management of Epilepsy Due to Hypothalamic Hamartomas.  75:29-42. 2017
  • Utility of the Autism Observation Scale for Infants in Early Identification of Autism in Tuberous Sclerosis Complex.  75:80-86. 2017
  • Primary Amebic Meningoencephalitis in Children: A Report of Two Fatal Cases and Review of the Literature.  70:75-79. 2017
  • Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors.  70:20-25. 2017
  • “Ivy Sign” and Moyamoya Disease in a Child With Neurofibromatosis Type 1.  70:80. 2017
  • Clinical Course of Six Children with GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.  59:81-84. 2016
  • Double Whammy: Trauma Leading to Sequential Bilateral Facial Nerve Palsy.  59:95-96. 2016
  • Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors.  58:67-74. 2016
  • Clinical Electroencephalographic Biomarker for Impending Epilepsy in Asymptomatic Tuberous Sclerosis Complex Infants.  54:29-34. 2016
  • Sjögren–Larsson Syndrome: A Neuro-Ichthyotic Disorder With Unique Magnetic Resonance Features.  62:73-74. 2016
  • In Memoriam: Bengt Arthur Hagberg, MD, PhD August 9, 1923-April 12, 2015.  53. 2015
  • Age of diagnosis in rett syndrome: Patterns of recognition among diagnosticians and risk factors for late diagnosis.  52:585-591.e2. 2015
  • The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders.  53:402-411. 2015
  • Pubertal development in rett syndrome deviates from typical females.  51:769-775. 2014
  • The American history of rett syndrome.  50:1-3. 2014
  • Valproate-induced pseudoatrophy: Expanding the clinical and imaging spectrum.  51:284-285. 2014
  • Tuberous sclerosis complex diagnostic criteria update: Recommendations of the 2012 international tuberous sclerosis complex consensus conference.  49:243-254. 2013
  • Tuberous sclerosis complex surveillance and management: Recommendations of the 2012 international tuberous sclerosis complex consensus conference.  49:255-265. 2013
  • Lennox-Gastaut syndrome symptomatic to hypothalamic hamartoma: Evolution and long-term outcome following surgery.  49:25-30. 2013
  • Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis Type 1.  48:447-453. 2013
  • Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopia.  45:274-278. 2011
  • Chorea as manifestation of epilepsia partialis continua in a child.  31:126-129. 2004
  • Chiari I malformation and neurofibromatosis type 1.  30:278-280. 2004
  • Duane's syndrome and giant parietal foramina.  30:75-76. 2004
  • Cutaneous manifestations and the Chiari I malformation.  29:250-252. 2003
  • Update on white matter genetic disorders (multiple letters) [2].  25:347-348. 2001
  • Möbius syndrome in infant exposed to cocaine in utero.  9:71-72. 1993
  • Bilateral periodic lateralized epileptiform discharges in Mycoplasma encephalitis.  8:292-294. 1992
  • Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophy.  8:432-436. 1992
  • Rett syndrome: Cerebellar pathology.  6:310-314. 1990
  • Pyruvate carboxylase deficiency: acute exacerbation after ACTH treatment of infantile spasms..  5:249-252. 1989
  • Rett syndrome: Biogenic amines and metabolites in postmortem brain.  5:357-362. 1989
  • Cerebellar hemorrhage in the term neonate: Developmental and neurologic outcome.  1:356-360. 1985
  • International Standard Serial Number (issn)

  • 0887-8994
  • Electronic International Standard Serial Number (eissn)

  • 1873-5150