| # | Title | Journal | Year | Citations |
|---|
|
| 1 | A Gut Feeling | Child Neurology Open | 2018 | 44 |
| 2 | Interleukin-6 Blockade With Tocilizumab in Anakinra-Refractory Febrile Infection-Related Epilepsy Syndrome (FIRES) | Child Neurology Open | 2020 | 44 |
| 3 | Seizures Related to Hypomagnesemia | Child Neurology Open | 2016 | 31 |
| 4 | Impact of Transcranial Direct Current Stimulation on Reading Skills of Children and Adolescents With Dyslexia | Child Neurology Open | 2018 | 31 |
| 5 | Spinal Muscular Atrophy: The Use of Functional Motor Scales in the Era of Disease-Modifying Treatment | Child Neurology Open | 2021 | 26 |
| 6 | Fatal Pediatric COVID-19 Case With Seizures and Fulminant Cerebral Edema | Child Neurology Open | 2021 | 22 |
| 7 | Epilepsy and EEG Phenotype of SLC13A5 Citrate Transporter Disorder | Child Neurology Open | 2020 | 21 |
| 8 | CEDNIK | Child Neurology Open | 2017 | 18 |
| 9 | Post COVID-19 Lymphocytic Hypophysitis: A Rare Presentation | Child Neurology Open | 2022 | 17 |
| 10 | Vein of Galen Aneurysmal Malformation in Neonates Presenting With Congestive Heart Failure | Child Neurology Open | 2016 | 16 |
| 11 | Maternal Race–Ethnicity, Immigrant Status, Country of Birth, and the Odds of a Child With Autism | Child Neurology Open | 2017 | 16 |
| 12 | Multiple Mitochondrial Dysfunctions Syndrome 4 Due to ISCA2 Gene Defects: A Review | Child Neurology Open | 2019 | 16 |
| 13 | Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy | Child Neurology Open | 2016 | 15 |
| 14 | Brain Inflammation in an Infant With Hemimegalencephaly, Escalating Seizures, and Epileptic Encephalopathy | Child Neurology Open | 2016 | 14 |
| 15 | Distal 22q11.2 Microduplication | Child Neurology Open | 2017 | 14 |
| 16 | Clinical Profile of Pediatric Neurological Disorders | Child Neurology Open | 2016 | 13 |
| 17 | Effect of Menstrual Cycle on Acute Intermittent Porphyria | Child Neurology Open | 2017 | 13 |
| 18 | A Novel SLC1A4 Mutation (p.Y191*) Causes Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly (SPATCCM) With Seizure Disorder | Child Neurology Open | 2019 | 13 |
| 19 | MECP2 Duplications in Symptomatic Females | Child Neurology Open | 2016 | 12 |
| 20 | Novel SCN1A and GABRA1 Gene Mutations With Diverse Phenotypic Features and the Question on the Existence of a Broader Spectrum of Dravet Syndrome | Child Neurology Open | 2017 | 12 |
| 21 | Spinal Cord Diffuse Midline Glioma in a 4-Year-Old Boy | Child Neurology Open | 2019 | 12 |
| 22 | Drug-Drug Interactions Between Cannabidiol and Lithium | Child Neurology Open | 2020 | 12 |
| 23 | Rapid Resolution of Enterovirus 71-Associated Opsoclonus Myoclonus Syndrome on Intravenous Immunoglobulin | Child Neurology Open | 2017 | 12 |
| 24 | A Pediatric Case of Sensory Predominant Guillain-Barré Syndrome Following COVID-19 Vaccination | Child Neurology Open | 2022 | 12 |
| 25 | Ketogenic Diet in Refractory Childhood Epilepsy | Child Neurology Open | 2018 | 11 |
| 26 | A Mutation in the Tubulin-Encoding TUBB3 Gene Causes Complex Cortical Malformations and Unilateral Hypohidrosis | Child Neurology Open | 2016 | 10 |
| 27 | Chromosome 12p Deletion Spanning the GRIN2B Gene Presenting With a Neurodevelopmental Phenotype | Child Neurology Open | 2016 | 10 |
| 28 | Two Novel KCNQ2 Mutations in 2 Families With Benign Familial Neonatal Convulsions | Child Neurology Open | 2017 | 10 |
| 29 | Novel LRPPRC Mutation in a Boy With Mild Leigh Syndrome, French–Canadian Type Outside of Québec | Child Neurology Open | 2017 | 10 |
| 30 | Afebrile Benign Convulsion Associated With Mild Gastroenteritis | Child Neurology Open | 2018 | 10 |
| 31 | Glycine Transporter 1 Encephalopathy From Biochemical Pathway to Clinical Disease: Review | Child Neurology Open | 2019 | 10 |
| 32 | Postinfectious Acute Disseminated Encephalomyelitis Associated With Antimyelin Oligodendrocyte Glycoprotein Antibody | Child Neurology Open | 2020 | 10 |
| 33 | Assessing Children With Disabilities Using WHO International Classification of Functioning, Disability and Health Child and Youth Version Activities and Participation D Codes | Child Neurology Open | 2015 | 9 |
| 34 | Therapeutic Effect of Steroids in Osmotic Demyelination of Infancy | Child Neurology Open | 2018 | 9 |
| 35 | Use of Cyclophosphamide in a Child With Fulminant Acute Disseminated Encephalomyelitis | Child Neurology Open | 2018 | 9 |
| 36 | Biotin-Thiamine-Responsive Basal Ganglia Disease: Case Report and Follow-Up of a Patient With Poor Compliance | Child Neurology Open | 2018 | 9 |
| 37 | Long-Term Exposure and Safety of a Novel Topical Rapamycin Cream for the Treatment of Facial Angiofibromas in Tuberous Sclerosis Complex: Results From a Single-Center, Open-Label Trial | Child Neurology Open | 2019 | 9 |
| 38 | Germinoma Mimicking Brain Inflammation: A Case Report | Child Neurology Open | 2019 | 9 |
| 39 | A Rare Case of Bartonella Encephalitis With Hemiplegia | Child Neurology Open | 2019 | 9 |
| 40 | Protocol and Feasibility-Randomized Trial of Telehealth Delivery for a Multicomponent Upper Extremity Intervention in Infants With Asymmetric Cerebral Palsy | Child Neurology Open | 2020 | 9 |
| 41 | Physical Therapy Intervention for a Child With Congenital Zika Virus Syndrome: A Case Report | Child Neurology Open | 2020 | 9 |
| 42 | Measuring the Barriers to Adherence With Neurology Clinic Appointments for Children With Epilepsy: A Pilot Study | Child Neurology Open | 2021 | 9 |
| 43 | Ketogenic Diet in Glut 1 Deficiency Through the Life Cycle: Pregnancy to Neonate to Preschooler | Child Neurology Open | 2021 | 9 |
| 44 | Pediatric Hereditary Neuralgic Amyotrophy | Child Neurology Open | 2016 | 8 |
| 45 | Visceral Hyperalgesia | Child Neurology Open | 2017 | 8 |
| 46 | Vibration-Assisted Home Training Program for Children With Spinal Muscular Atrophy | Child Neurology Open | 2018 | 8 |
| 47 | Two Cases of Guillain-Barré Syndrome Variants Presenting With Dysautonomia | Child Neurology Open | 2019 | 8 |
| 48 | Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without Encephalopathy | Child Neurology Open | 2019 | 8 |
| 49 | CLIPPERS Spectrum Disorder: A Rare Pediatric Neuroinflammatory Condition | Child Neurology Open | 2019 | 8 |
| 50 | Expanded Phenotypic Definition Identifies Hundreds of Potential Causative Genes for Leukodystrophies and Leukoencephalopathies | Child Neurology Open | 2020 | 8 |
