Epidemiological, Clinical, Etiological, and Therapeutic Aspects of Cerebral Palsy in Dakar

2024-8-23

The Effectiveness of Botulinum Toxin Injections to the Extremities in the Pediatric Population with Severe Cerebral Palsy: A Systematic Review

2024-8-16

Anterior Cutaneous Neurectomy—Child's Play?

2024-8-9

Malformations of the Spinal Cord: From Genetics to Diagnosis and Rehabilitation

2024-8-9

Area Postrema Syndrome as the Onset of Neuromyelitis Optica in a Pediatric Patient: Case Report

2024-8-7

Acute Onset, Relapsing–Remitting Choreiform Movement Disorder in A Girl with 22q11.2 Deletion Syndrome

2024-7-31

The Spectrum of Childhood-Onset Lower Motor Neuron Disease of Spinal Muscular Atrophy Phenotype Associated with Survival Motor Neuron-2 Gene Deletion

2024-7-30

Examining Neural Correlates of Sexual Preferences between Persian Homo- and Heterosexual Males Using Psychological Assessments and Functional Magnetic Resonance Imaging in Specifying Cognitive Map: A Limited and Cross-sectional Study

2024-7-30

Infantile Idiopathic Intracranial Hypertension: Case Report of an 8-Month-Old Child

2024-7-30

Comparison Efficacy of Phenobarbital versus Levetiracetam in Acute Neonatal Seizures: A Randomized Control Trial

2024-7-10

A Middle-Aged Patient Living with HIV (PLHIV), Presented with Persistent Hiccups, Imbalance, and Multifocal Myoclonus Secondary to Disseminated Tuberculosis

2024-7-10

Severe Hypoplasia/Aplasia of the Medullary Arcuate Nucleus in a 4-Month-Old Patient with Sudden Infant Death Syndrome

2024-7-4

Spontaneous Simultaneous Bilateral Intraparenchymal Hemorrhage in a Child with Sickle Cell Disease

2024-7-4

SCN8A Encephalopathy with a Significant Long-Term Response to Lacosamide

2024-6-26

CAPOS Syndrome with Fluctuating Symptoms

2024-6-26

Journal of Pediatric Neurology

2024-6-20

Paroxysmal Kinesigenic Dyskinesia Secondary to Novel Variant in PRRT2: A Case Report

2024-6-3

Clinical Response of Levodopa in CTNNB1-Related Dystonia

2024-6-3

Anomalies of Midbrain Hindbrain Development: Midbrain Clefts, Cerebellar Nodular Heterotopia with Overlying Dysgenesis, Cerebellar Foliation Disorder, Pontine Tegmental Cap Dysplasia; Joubert Syndrome; Lhermitte Duclos Syndrome. Diagnosis, Classification and Rehabilitation Hypothesis

2024-5-30

The Role of Electroencephalography in the Prediction of Relapse of Febrile Convulsion in Patients Aged Between 6 to 60 Months: A Prospective Cohort Study

2024-5-30

Primary Amoebic Meningoencephalitis with Progression to Brain Death Following Naegleria Fowleri Infection in a Teenage Female

2024-5-30

Anomalies of Midbrain/Hindbrain Development and Related Disabilities: Pontocerebellar Hypoplasia, Congenital Disorders of Glycosylation, and Cerebellar Hemisphere Hypoplasia

2024-5-29

Polymicrogyria, Cobblestone Malformations, and Tubulin Mutation (Overmigration beyond Pial Limiting Membrane): Diagnosis, Treatment, and Rehabilitation Approach

2024-5-29

Periventricular Heterotopias: Neuroependymal Abnormalities

2024-5-29

Anomalies of the Craniocervical Junction (Chiari Malformations)

2024-5-29

Defects of Midbrain/Hindbrain Development: Defects of Anteroposterior and Dorsoventral Patterning

2024-5-29

Knobloch Syndrome Type 1 with a Novel Pathogenic Variant in the COL18A1 Gene: Case Report and Review of the Literature

2024-5-29

Cerebral Malformations Related to Coronavirus Disease 2019 during Pregnancy

2024-5-13

Megalencephaly: Classification, Genetic Causes, and Related Syndromes

2024-5-11

Anomalies of the Mesenchyme (Meninges and Skull)—Defects of Neural Tube Closure: Cephalocele and Other Calvarial and Skull Base Defects; Intracranial Lipomas; Arachnoid Cysts; Nonsyndromic and Syndromic Craniosynostoses

2024-5-11

Schizencephaly: Etiopathogenesis, Classification, Therapeutic, and Rehabilitative Approach

2024-5-11

Anomalies of Midbrain/Hindbrain Development: Malformations of Cerebellum: Diagnosis, Classification, and Rehabilitative Hypothesis

2024-5-11

Congenital/Primitive Hydrocephalus: Classification, Clinical Aspects, and Rehabilitation Approach

2024-5-11

Malformations of the Cerebral Commissures

2024-5-11

Lissencephaly, Pachygyrias, Band Heterotopias, RELN Pathway, and ARX Mutations (Incomplete Neuron Migration)

2024-5-11

L1 Syndrome-Associated Phenotypes and a Novel L1CAM Variant: A Clinical Report

2024-4-25

Phenotypic Variability Related to Mutations in Riboflavin Transporter in Brazilian Children: Pediatric Case Series

2024-4-24

Investigation of the Relationship between Burnout Level and Psychological Resilience in Parents of Children with Down Syndrome

2024-4-24

Focal Cortical Dysplasia: Diagnosis, Classification, and Treatment Options

2024-4-1

At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation

2024-4-1

At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System

2024-4-1

Foreword: A Special Issue on Central Nervous System Malformations

2024-4-1

Introduction: A Practical Guide to Central Nervous System Malformations—From Genetics, to Diagnosis and Treatment

2024-4-1

Holoprosencephaly: The Disease and Its Related Disabilities

2024-4-1

Microcephaly and Its Related Syndromes: Classification, Genetic, Clinical, and Rehabilitative Considerations

2024-4-1

Be Alert to ALERD: Acute Leukoencephalopathy with Restricted Diffusion—Atypical Presentation of a Rare Case

2024-3-18

Report of a New Pediatric Patient with the SLC1A4 Variant and a Brief Review of the Literature

2024-3-1