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Walk the evidence base by book and chapter — the raw source passages that ground Ask, Differential, and the rest.

• "Restricted Diffusion" within the Splenium of the Corpus Callosum: A Potential Pitfall in Young Infants on 3T Imaging and Marker of Normal Myelin Maturation.1 passage
• 4H Leukodystrophy: A Brain Magnetic Resonance Imaging Scoring System.1 passage
• 4H Leukodystrophy: Lessons from 3T Imaging.1 passage
• A 5-Year Follow-Up of Triple-Seronegative Myasthenia Gravis Successfully Treated with Tacrolimus Therapy.1 passage
• A Case Report on Juvenile Neuromyelitis Optica: Early Onset, Long Remission Period, and Atypical Treatment Response.1 passage
• A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic Aspects.1 passage
• A De Novo Dominant Negative Mutation in DNM1L Causes Sudden Onset Status Epilepticus with Subsequent Epileptic Encephalopathy.1 passage
• A De Novo Missense Variant in POU3F2 Identified in a Child with Global Developmental Delay.1 passage
• A Female Patient with Xq28 Microduplication Presenting with Myotubular Myopathy, Confirmed with a Custom-Designed X-array.1 passage
• A Missense De Novo Variant in the CASK-interactor KIRREL3 Gene Leading to Neurodevelopmental Disorder with Mild Cerebellar Hypoplasia.1 passage
• A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing Panencephalitis.1 passage
• A Novel Homozygous Mutation in the FUCA1 Gene Highlighting Fucosidosis as a Cause of Dystonia: Case Report and Literature Review.1 passage
• A Novel Hypomorphic CSF1R Gene Mutation in the Biallelic State Leading to Fatal Childhood Neurodegeneration.1 passage
• A Novel Variant in the HINT1 Gene in a Girl with Autosomal Recessive Axonal Neuropathy with Neuromyotonia: Thorough Neurological Examination Gives the Clue.1 passage
• A Pilot Study Evaluating Cerebral Vasculitis in Kawasaki's Disease.1 passage
• A Presentation of Pediatric Sjögren's Syndrome with Abducens Nerve Palsy.1 passage
• A Rare Presentation of Neurobrucellosis in a 6-Year-Old Pediatric Patient with Sagittal Sinus Thrombosis.1 passage
• A Revisited Diagnosis of Collagen VI Related Muscular Dystrophy in a Patient with a Novel COL6A2 Variant and 21q22.3 Deletion.1 passage
• A Systematic Review of the Efficacy of Levetiracetam in Neonatal Seizures.1 passage
• A Very Rare Etiology of Hypotonia and Seizures: Congenital Glutamine Synthetase Deficiency.1 passage
• A p.Arg499His Mutation in SPAST Is Associated with Infantile Onset Ascending Spastic Paralysis Complicated with Dysarthria and Anarthria.1 passage
• A painful stiff neck following an ear, nose, and throat surgical procedure: case report.1 passage
• ADHD: Current Concepts and Treatments in Children and Adolescents.1 passage
• AGRN Gene Mutation Leads to Congenital Myasthenia Syndromes: A Pediatric Case Report and Literature Review.1 passage
• Absent Thalami Caused by a Homozygous EARS2 Mutation: Expanding Disease Spectrum of LTBL.1 passage
• Access to Intrathecal Baclofen Treatment for Children with Cerebral Palsy in European Countries: An SCPE Survey Reveals Important Differences.1 passage
• Accuracy of Flash Glucose Monitoring in a Patient with Dravet Syndrome on a Ketogenic Diet.1 passage
• Activin A and Acvr2b mRNA from Umbilical Cord Blood Are Not Reliable Markers of Mild or Moderate Neonatal Hypoxic-Ischemic Encephalopathy.1 passage
• Activin A in perinatal brain injury.1 passage
• Acupuncture in Adult and Pediatric Headache: A Narrative Review.1 passage
• Acute Cerebellitis and Atypical Posterior Reversible Encephalopathy Syndrome Associated with Methadone Intoxication.1 passage
• Acute Disseminated Encephalomyelitis followed by Optic Neuritis: A Rare Syndrome of Uncertain Treatment and Prognosis.1 passage
• Acute Sensory Neuronopathy following Enterovirus Infection in a 3-Year-Old Girl.1 passage
• Adenosine Kinase Deficiency: Report and Review.1 passage
• Adverse Effects of Treatment with Valproic Acid during the Neonatal Period.1 passage
• Age-Dependency of Location of Epileptic Foci in "Continuous Spike-and-Waves during Sleep": A Parallel to the Posterior-Anterior Trajectory of Slow Wave Activity.1 passage
• Age-Dependent Seroprevalence of JCV Antibody in Children.1 passage
• Age-Related Changes and Reference Values of Bicaudate Ratio and Sagittal Brainstem Diameters on MRI.1 passage
• Aicardi Syndrome: Key Fetal MRI Features and Prenatal Differential Diagnosis.1 passage
• Alternating Hemiplegia of Childhood in a Child Harboring a Novel TBC1D24 Mutation: Case Report and Literature Review.1 passage
• An Unusual Cause of Chronic Headache in an Adolescent Boy: A Case Report.1 passage
• Another Piece of the Puzzle of Anomalous Connectivity in Joubert's Syndrome.1 passage
• Antiquitin Deficiency with Adolescent Onset Epilepsy: Molecular Diagnosis in a Mother of Affected Offsprings.1 passage
• Aphasia and a Dual-Stream Language Model in a 4-Year-Old Female with Landau-Kleffner Syndrome.1 passage
• Applications of optical coherence tomography in pediatric clinical neuroscience.1 passage
• Are Epileptic Spasms a Seizure Type for the Insular Region?1 passage
• Arrested Hydrocephalus in Childhood: Case Series and Review of the Literature.1 passage
• Arterial Ischemic Stroke-Peculiarities of Clinical Presentation and Risk Factors in Indian Children.1 passage
• Asparagine Synthetase Deficiency with Intracranial Hemorrhage Can Mimic Molybdenum Cofactor Deficiency.1 passage
• Assessing and Improving Documentation of Pediatric Brain Death Determination within an Electronic Health Record.1 passage
• Atypical Neurologic Phenotype and Novel SLC30A10 Mutation in Two Brothers with Hereditary Hypermanganesemia.1 passage
• Atypical Presentation of Fulminating Subacute Sclerosing Panencephalitis: A Case Series.1 passage
• Auditory Processing in Children with Migraine: A Controlled Study.1 passage
• Autopsy Report of a Woman with Infantile Alexander Disease Who Survived 39 Years.1 passage
• Autosomal Recessive Primary Microcephaly (MCPH): An Update.1 passage
• Axenfeld-Rieger Anomaly and Neuropsychiatric Problems-More than Meets the Eye.1 passage
• B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker-Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss.1 passage
• Bedside Ultrasound-Guided Percutaneous Needle Aspiration of Intra- and Extra-Axial Intracranial Hemorrhage in Neonates.1 passage
• Beta Propellar Protein-Associated Neurodegeneration: A Rare Cause of Infantile Autistic Regression and Intracranial Calcification.1 passage
• Biallelic Mutations in MTPAP Associated with a Lethal Encephalopathy.1 passage
• Biallelic Mutations in SLC1A2; an Additional Mode of Inheritance for SLC1A2-Related Epilepsy.1 passage
• Bilateral Striatal Necrosis after Sydenham's Chorea in a 7-Year-Old Boy: A 2-Year Follow-Up.1 passage
• Bilateral Striatal Necrosis with Polyneuropathy with a Novel SLC25A19 (Mitochondrial Thiamine Pyrophosphate Carrier OMIMI*606521) Mutation: Treatable Thiamine Metabolic Disorder-A Report of Two Indian Cases.1 passage
• Bilateral frontoparietal polymicrogyria: a novel GPR56 mutation and an unusual phenotype.1 passage
• Botulinum Toxin in Children with Cerebral Palsy: An Update.1 passage
• Brain Aneurysms in the Pediatric Population of Slovenia: A Case Series.1 passage
• Brain Perfusion Is Increased at Term in the White Matter of Very Preterm Newborns and Newborns with Congenital Heart Disease: Does this Reflect Activated Angiogenesis?1 passage
• Brain magnetic resonance imaging in acute phase of pandemic influenza A (H1N1) 2009--associated encephalopathy in children.1 passage
• Brainstem disconnection: two additional patients and expansion of the phenotype.1 passage
• CDKL5 Gene-Related Epileptic Encephalopathy in Estonia: Four Cases, One Novel Mutation Causing Severe Phenotype in a Boy, and Overview of the Literature.1 passage
• Cannabidiol Interacts Significantly with Everolimus-Report of a Patient with Tuberous Sclerosis Complex.1 passage
• Cardiac Abnormalities in Congenital and Childhood Myotonic Muscular Dystrophy Type 1.1 passage
• Cardiac Myxoma as a Rare Cause of Pediatric Arterial Ischemic Stroke: Case Report and Literature Review.1 passage
• Cardiac function in types II and III spinal muscular atrophy: should we change standards of care?1 passage
• Cerebral Autoregulation and Neurovascular Coupling after Craniospinal Irradiation in Long-Term Survivors of Malignant Pediatric Brain Tumors of the Posterior Fossa.1 passage
• Cerebral Hyperperfusion in a Child with Stroke-Like Migraine Attacks after Radiation Therapy Syndrome.1 passage
• Cerebral Insufficiency Caused by Diazoxide in a Premature Neonate with Congenital Hyperinsulinism.1 passage
• Cerebral Toxocariasis as a Cause of Epilepsy: A Pediatric Case.1 passage
• Change of Cerebral Oxygenation during Surfactant Treatment in Preterm Infants: "LISA" versus "InSurE" Procedures.1 passage
• Changes of White Matter Diffusion Anisotropy in Response to a 6-Week iPad Application-Based Occupational Therapy Intervention in Children with Surgically Treated Hydrocephalus: A Pilot Study.1 passage
• Changing Landscape of Dravet Syndrome Management: An Overview.1 passage
• Characteristics of Pediatric Stroke and Association of Delayed Diagnosis with Mortality in a Mexican Tertiary Care Hospital.1 passage
• Chiari Type 1 Deformity in Children: Pathogenetic, Clinical, Neuroimaging, and Management Aspects.1 passage
• Childhood Dystonia-Parkinsonism Following Infantile Spasms-Clinical Clue to Diagnosis in Early Beta-Propeller Protein-Associated Neurodegeneration.1 passage
• Childhood Stroke: Long-Term Outcomes and Health-Related Quality of Life with a Special Focus on the Development of Epilepsy.1 passage
• Childhood-Onset Multifocal Motor Neuropathy with IgM Antibodies to Gangliosides GM1: A Case Report with Poor Outcome.1 passage
• Children's Headache: Drawings in the Diagnostic Work Up.1 passage
• Chudley-McCullough Syndrome: Variable Clinical Picture in Twins with a Novel GPSM2 Mutation.1 passage
• Cleft Palate as Distinguishing Feature in a Patient with GABRB3 Epileptic Encephalopathy.1 passage
• Clinical Assessment of Dysarthria in Children with Cerebellar Syndrome Associated with PMM2-CDG.1 passage
• Clinical Characteristics and Genotype-Phenotype Correlation in Children with KMT2E Gene-Related Neurodevelopmental Disorders: Report of Two New Cases and Review of Published Literature.1 passage
• Clinical Conundrums When Integrating the QbTest into a Standard ADHD Assessment of Children and Young People.1 passage
• Clinical Features and Outcomes of Streptococcus pneumoniae Meningitis in Children: A Retrospective Analysis of 26 Cases in China.1 passage
• Clinical Features, Therapeutic Response, and Follow-Up in Pediatric Anti-N-Methyl-D-Aspartate Receptor Encephalitis: Experience from a Tertiary Care University Hospital in India.1 passage
• Clinical Phenotype in an Early-Onset French Pediatric Population: Charcot-Marie-Tooth's Disease Type 2A.1 passage
• Clinical and Biochemical Pitfalls in the Diagnosis of Peroxisomal Disorders.1 passage
• Clinical and Electroencephalographic Correlates in Pediatric Cardiac Arrest: Experience at a Tertiary Care Center.1 passage
• Clinical and Genetic Aspects of Juvenile Onset Pompe Disease.1 passage
• Clinical and Genetic Features of Congenital Myasthenic Syndromes due to CHAT Mutations: Case Report and Literature Review.1 passage
• Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 Gene.1 passage
• Clinical, Electrodiagnostic, and Genetic Features of Tangier Disease in an Adolescent Girl with Presentation of Peripheral Neuropathy.1 passage
• Clinico-Radiological Correlation in 26 Egyptian Children with Glutaric Acidemia Type 1.1 passage
• Cognitive Development in Pediatric Epilepsy Surgery.1 passage
• Combined Muscle Biopsy and Comprehensive Electrophysiology in General Anesthesia is Valuable in Diagnosis of Neuromuscular Disease in Children.1 passage
• Comparative Analysis of Cerebral Magnetic Resonance Imaging Changes in Nontreated Infantile, Juvenile and Adult Patients with Niemann-Pick Disease Type C.1 passage
• Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor.1 passage
• Congenital Amegakaryocytic Thrombocytopenia Type II Presenting with Multiple Central Nervous System Anomalies.1 passage
• Congenital Disorders of Autophagy: What a Pediatric Neurologist Should Know.1 passage
• Congenital Glioblastoma Multiforme: An Unusual and Challenging Tumor.1 passage
• Congenital Lymphatic Malformation and Aortic Aneurysm in a Patient with TSC2 Mutation.1 passage
• Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Gene Mutation: A Rare Cause of Neonatal-Onset Neurodegenerative Disorder.1 passage
• Considering Valproate as a Risk Factor for Rapid Exacerbation of Complex Movement Disorder in Progressed Stages of Late-Infantile CLN2 Disease.1 passage
• Continuous myocloni and tonic spasms in a 2-month-old infant with enterovirus 71 brain stem encephalitis.1 passage
• Cooccurrence of Two Different Genetic Diseases: A Case of Valproic Acid Hepatotoxicity in Nicolaides-Baraitser Syndrome (SMARCA2 Mutation)-Due to a POLG1-Related Effect?1 passage
• Cranial Ultrasound Is an Important Tool in the Recognition of Life-Threatening Infratentorial Hemorrhage in Newborns.1 passage
• Crossed Pontine Hemiatrophy Associated with Unilateral Cerebellar Hemorrhage in Premature Infants.1 passage
• Cystic Encephalomalacia following Vasculopathy and Vasospasm of Proximal Intracranial Arteries Due to Pneumococcal Meningitis in a Infant.1 passage
• Cytosolic Phosphoenolpyruvate Carboxykinase Deficiency: Cause of Hypoglycemia-Induced Seizure and Death.1 passage
• Daily Functioning and Quality of Life in Patients with Sjögren-Larsson Syndrome.1 passage
• Decision-Making Regarding Ventilator Support in Children with SMA Type 1-A Cross-Sectional Survey among Physicians.1 passage
• Decompressive craniectomy after severe traumatic brain injury in children: complications and outcome.1 passage
• Developmental Regression and Epilepsy of Infancy with Migrating Focal Seizures Caused by TBCD Mutation: A Case Report and Review of the Literature.1 passage
• Diagnosis and Treatment of Tuberous Sclerosis Manifestations in Children: A Multicenter Study.1 passage
• Diagnostic Considerations in Acute Disseminated Encephalomyelitis and the Interface with MOG Antibody.1 passage
• Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience.1 passage
• Diagnostic Utility of Whole Exome Sequencing in the Neuromuscular Clinic.1 passage
• Differential Analysis of Bone Density in Children and Adolescents with Neuromuscular Disorders and Cerebral Palsy.1 passage
• Differential Diagnosis of Cerebellar Atrophy in Childhood: An Update.1 passage
• Differentially Regulated Cell-Free MicroRNAs in the Plasma of Friedreich's Ataxia Patients and Their Association with Disease Pathology.1 passage
• Difficulty in Distinguishing Posterior Reversible Encephalopathy Syndrome, Hypoxic-Ischemic Insult, and Acute Toxic Leukoencephalopathy in Children.1 passage
• Diffusion-Weighted Imaging of Periventricular Leukomalacia in Very Young Children: Assessment of Peritrigonal Stripe of Restricted Diffusion.1 passage
• Does Botulinum Toxin A Treatment Enhance the Walking Pattern in Idiopathic Toe-Walking?1 passage
• Does Co-occurred Cerebral Palsy Change the Prognosis of West Syndrome?1 passage
• Dog-Assisted Therapy in Neurorehabilitation of Children with Severe Neurological Impairment: An Explorative Study.1 passage
• Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech Development.1 passage
• Dystrophinopathies and Limb-Girdle Muscular Dystrophies.1 passage
• EPG5 Variants with Modest Functional Impact Result in an Ameliorated and Primarily Neurological Phenotype in a 3.5-Year-Old Patient with Vici Syndrome.1 passage
• Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review.1 passage
• Early Onset, Long Illness Duration, Epilepsy Type, and Polypharmacy Have an Adverse Effect on Psychosocial Outcome in Children with Epilepsy.1 passage
• Early Prenatal MRI of Cervical "Abortive" Myelocystocele: Case Report and Review of the Literature.1 passage
• Early Retinal Findings Following Cooling in Neonatal Encephalopathy.1 passage
• Early Seizure Freedom Is a Prognostic Factor for Survival in Patients with West Syndrome.1 passage
• Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.1 passage
• Early-Onset Severe Encephalopathy with Epilepsy: The BRAT1 Gene Should Be Added to the List of Causes.1 passage
• Effect of Hemoconcentration on Dural Sinus Computed Tomography Density in a Pediatric Population.1 passage
• Effect of Levetiracetam Monotherapy in Nonlesional Focal Childhood Epilepsy.1 passage
• Effect of Long-Term Repeated Interval Rehabilitation on the Gross Motor Function Measure in Children with Cerebral Palsy.1 passage
• Effect of Sunlight Exposure on Bone Mineral Density in Children with Severe Disability.1 passage
• Effect of l-Arginine in One Patient with Peroxisome Biogenesis Disorder due to PEX12 Deficiency.1 passage
• Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies: first experiences.1 passage
• Effectiveness of Electroconvulsive Therapy for Refractory Status Epilepticus in Febrile Infection-Related Epilepsy Syndrome.1 passage
• Effects of Modified Constraint-Induced Movement Therapy in Real-World Arm Use in Young Children with Unilateral Cerebral Palsy: A Single-Blind Randomized Trial.1 passage
• Efficacy of a Brief Psychoeducational Intervention for Mothers of Children with Breath-Holding Spells: A Randomized Controlled Pilot Trial.1 passage
• Efficiency of a Combination of Pharmacological Treatment and Nondrug Interventions in Childhood Narcolepsy.1 passage
• Epilepsy and autoimmunity in pediatric patients.1 passage
• Epilepsy in Nicolaides-Baraitser Syndrome: Review of Literature and Report of 25 Patients Focusing on Treatment Aspects.1 passage
• Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral Phenotype.1 passage
• Epileptic Encephalopathy, Myoclonus-Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene.1 passage
• Epileptic Phenotype of Two Siblings with Asparagine Synthesis Deficiency Mimics Neonatal Pyridoxine-Dependent Epilepsy.1 passage
• Etiological and Clinical Profile of Acute Nonbacterial Encephalitis in Children: A Single-Center Prospective Study.1 passage
• Etiology and Long-Term Outcomes of Late-Onset Infantile Spasms.1 passage
• European and Australian Cerebral Palsy Surveillance Networks Working Together for Collaborative Research.1 passage
• Evaluating an Association between Ampicillin and Intraventricular Hemorrhage in Preterm Infants.1 passage
• Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years.1 passage
• Expanding Clinical Phenotype of TRAPPC12-Related Childhood Encephalopathy: Two Cases and Review of Literature.1 passage
• Expanding Phenotypic Spectrum of Cerebral Aspartate-Glutamate Carrier Isoform 1 (AGC1) Deficiency.1 passage
• Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIA.1 passage
• Extremely Early Onset Transthyretin Familial Amyloid Polyneuropathy with a Leu55Pro Mutation: A Pediatric Case Report and Literature Review.1 passage
• Eye Findings on Vigabatrin and Taurine Treatment in Two Patients with Succinic Semialdehyde Dehydrogenase Deficiency.1 passage
• Eyes on MEGDEL: distinctive basal ganglia involvement in dystonia deafness syndrome.1 passage
• Factors Influencing Motor Outcome of Hippotherapy in Children with Cerebral Palsy.1 passage
• Familial Precocious Fetal Abnormal Cortical Sulcation.1 passage
• Febrile Infection-Related Epilepsy Syndrome (FIRES) with Multifocal Subcortical Infarcts, A New Imaging Phenotype.1 passage
• Febrile Infection-Related Epilepsy Syndrome: Clinical Review and Hypotheses of Epileptogenesis.1 passage
• Febrile and postinfectious myoclonus: case reports and review of the literature.1 passage
• Forkhead box G1 gene haploinsufficiency: an emerging cause of dyskinetic encephalopathy of infancy.1 passage
• From Genetics to Genomics: A Short Introduction for Pediatric Neurologists.1 passage
• Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 Deletion.1 passage
• Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease.1 passage
• Genotype-Phenotype Dissociation in Two Taiwanese Children with Molybdenum Cofactor Deficiency Caused by MOCS2 Mutation.1 passage
• Gillespie's Syndrome with Minor Cerebellar Involvement and No Intellectual Disability Associated with a Novel ITPR1 Mutation: Report of a Case and Literature Review.1 passage
• Gross Motor Function in Children with Congenital Zika Syndrome.1 passage
• HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy-Report of 11 Patients.1 passage
• Health-Related Quality of Life in Children and Adolescents with Cerebral Palsy: A Secondary Analysis of the DISABKIDS Questionnaire in the Field-Study Cerebral Palsy Subgroup.1 passage
• Health-Related Quality of Life of Children/Adolescents with Vertigo: Retrospective Study from the German Center of Vertigo and Balance Disorders.1 passage
• Hepatic Involvement in Aicardi-Goutières Syndrome.1 passage
• Hereditary Dopamine Transporter Deficiency Syndrome: Challenges in Diagnosis and Treatment.1 passage
• Hereditary Orotic Aciduria and the Excretion of Orotidine.1 passage
• Hereditary orotic aciduria with epilepsy and without megaloblastic anemia.1 passage
• High Incidence of Renal Stones in Severely Disabled Children with Epilepsy Treated with Topiramate.1 passage
• Homonymous Hemianopia in Children and Adolescents: An MRI Study.1 passage
• Homozygous TANGO2 Single Nucleotide Variants Presenting with Additional Manifestations Resembling Alternating Hemiplegia of Childhood-Expanding the Phenotype of a Recently Reported Condition.1 passage
• Horner Syndrome in Children: A Clinical Condition with Serious Underlying Disease.1 passage
• Hydrocephalus Revisited: New Insights into Dynamics of Neurofluids on Macro- and Microscales.1 passage
• Hyperkinetic Seizures with Ictal Fear as Localizing Ictal Signs in MRI-Negative Medial Frontal Lobe Epilepsy.1 passage
• Hypomyelinating Leukodystrophy due to HSPD1 Mutations: A New Patient.1 passage
• Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients.1 passage
• Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.1 passage
• Identification of Copy Number Variation by Array-CGH in Portuguese Children and Adolescents Diagnosed with Autism Spectrum Disorders.1 passage
• Idiopathic Acute Transverse Myelitis in Children: A Retrospective Series.1 passage
• Imaging Pediatric Multiple Sclerosis-Challenges and Recent Advances.1 passage
• Imaging in X-Linked Adrenoleukodystrophy.1 passage
• Impact of Hippotherapy on Gross Motor Function and Quality of Life in Children with Bilateral Cerebral Palsy: A Randomized Open-Label Crossover Study.1 passage
• Improving Management of Infantile Spasms by Adopting Implementation Science.1 passage
• Infantile Basal Ganglia Stroke after Mild Head Trauma Associated with Mineralizing Angiopathy of Lenticulostriate Arteries: An Under Recognized Entity.1 passage
• Infantile Hemangioma of the Posterior Fossa in a Newborn: Early Management and Long-Term Follow-up.1 passage
• Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 Mutation.1 passage
• Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach?1 passage
• Inflammatory Characteristics of Monocytes from Pediatric Patients with Tuberous Sclerosis.1 passage
• Inherited Disorders of Neurotransmitters: Classification and Practical Approaches for Diagnosis and Treatment.1 passage
• Inherited and Acquired Muscle Weakness: A Moving Target for Diagnostic Muscle Biopsy.1 passage
• Interhemispheric Lipoma, Callosal Anomaly, and Malformations of Cortical Development: A Case Series.1 passage
• Interpeduncular Heterotopia and Brain Stem Cleft: An Isolated Finding Not Associated with Joubert Syndrome.1 passage
• Intracranial hypertension in siblings with infantile hypercalcemia.1 passage
• Intrathecal Administration of Nusinersen in Pediatric SMA Patients with and without Spine Deformities: Experiences and Challenges over 3 Years in a Single Center.1 passage
• Is Asymmetry of the Pons Associated with Hand Function and Manual Ability after Arterial Ischemic Stroke in Children?1 passage
• Is Brain MRI Needed in Diagnostic Evaluation of Mild Intellectual Disability?1 passage
• Is Exercise-Induced Fatigue a Problem in Children with Duchenne Muscular Dystrophy?1 passage
• Is Tadpole Pupil in an Adolescent Girl Caused by Denervation Hypersensitivity?1 passage
• Isolated Congenital Absence of Cranial Nerves: Report of Two Cases.1 passage
• Japanese Encephalitis Virus-Induced Anti-N-Methyl-D-Aspartate Receptor Encephalitis: A Case Report and Review of Literature.1 passage
• Jumping Mechanography is a Suitable Complementary Method to Assess Motor Function in Ambulatory Boys with Duchenne Muscular Dystrophy.1 passage
• Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular Disorders.1 passage
• Juvenile Chronic Inflammatory Demyelinating Polyneuropathy Epidemiology in Sardinia, Insular Italy.1 passage
• Ketamine Infusion for Super Refractory Status Epilepticus in Alternating Hemiplegia of Childhood.1 passage
• Ketogenic Diet for KARS-Related Mitochondrial Dysfunction and Progressive Leukodystrophy.1 passage
• Lacosamide Lowers Valproate and Levetiracetam Levels.1 passage
• Lafora Disease: A Review of Molecular Mechanisms and Pathology.1 passage
• Lennox-Gastaut Syndrome: A State of the Art Review.1 passage
• Letter to the Editor Regarding the Article "Whole-Exome Sequencing in NF1-Related West's Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy".1 passage
• Lidocaine treatment in refractory status epilepticus resulting from febrile infection-related epilepsy syndrome: a case report and follow-up.1 passage
• Lip Forces and Chewing Efficiency in Children with Peripheral Facial Paralysis.1 passage
• Long-Term Health Outcomes and Health-Related Quality of Life in Adolescents from a Cohort of Extremely Premature Infants Born at Less Than 27 Weeks of Gestation in Northern Germany.1 passage
• Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 Gene.1 passage
• Longitudinally Extensive Transverse Myelitis (LETM) and Myopericarditis in a 7-Month-Old Child with SARs-CoV-2 Infection.1 passage
• Low Serum Level α-Synuclein and Tau Protein in Autism Spectrum Disorder Compared to Controls.1 passage
• Lumbar Puncture Opening Pressure in Patients with Spinal Muscular Atrophy.1 passage
• MOG Spectrum Disorders and Role of MOG-Antibodies in Clinical Practice.1 passage
• Management of Neurological Emergencies in Children: An Updated Overview.1 passage
• Management of Primary Tectal Plate Low-Grade Glioma in Pediatric Patients: Results of the Multicenter Treatment Study SIOP-LGG 2004.1 passage
• Methods in pediatric sleep research and sleep medicine.1 passage
• Mild Encephalitis/Encephalopathy with Reversible Splenial Lesion (MERS) due to Cytomegalovirus: Case Report and Review of the Literature.1 passage
• Mobility Characteristics of Children with Spastic Paraplegia Due to a Mutation in the KIF1A Gene.1 passage
• Monitoring Criteria of Intracranial Lesions in Children Post Mild or Moderate Head Trauma.1 passage
• Monocyte Chemoattractant Protein (MCP)-1 in Rotavirus-Associated White Matter Injury in Newborns.1 passage
• Moyamoya Syndrome in an Infant with Aicardi-Goutières and Williams Syndromes: A Case Report.1 passage
• Multicenter Experience with Nusinersen Application via an Intrathecal Port and Catheter System in Spinal Muscular Atrophy.1 passage
• Multimodal Assessment Reveals Late-Onset Hemispheric Shift of Language in a Child with Meningocerebral Dysplasia.1 passage
• Multiple Causes of Pediatric Early Onset Chorea-Clinical and Genetic Approach.1 passage
• Multiple Sclerosis with Onset Younger Than 10 Years in Turkey.1 passage
• Muscle-Specific Kinase Autoimmune Myasthenia Gravis: Report of a Pediatric Case and Literature Review.1 passage
• Mycoplasma Pneumoniae and Antibodies against Galactocerebroside in a 9-Year-Old Boy with Encephalitis.1 passage
• Myelin Oligodendrocyte Glycoprotein-Associated Pediatric Central Nervous System Demyelination: Clinical Course, Neuroimaging Findings, and Response to Therapy.1 passage
• N-Methyl-D-Aspartate Receptor Encephalitis with Psychiatric Symptoms and an Ovarian Teratoma Detected by MRI in a 17-Year-Old Girl.1 passage
• Narcolepsy during Childhood: An Update.1 passage
• Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases.1 passage
• Neonatal Herpes Simplex Virus-1 Recurrence with Central Nervous System Disease in Twins after Completion of a Six-Month Course of Suppressive Therapy: Case Report.1 passage
• Neonatal Onset of Epilepsy of Infancy with Migrating Focal Seizures Associated with a Novel GABRB3 Variant in Monozygotic Twins.1 passage
• Neonatal Seizures-Are We there Yet?1 passage
• Neonatal Seizures: A Review of Outcomes and Outcome Predictors.1 passage
• Neonatal Vitamin D Status Is Associated with the Severity of Brain Injury in Neonatal Hypoxic-Ischemic Encephalopathy: A Pilot Study.1 passage
• Neurodevelopmental Disorders and Array-Based Comparative Genomic Hybridization: Sensitivity and Specificity using a Criteria Checklist for Genetic Test Performance.1 passage
• Neurodevelopmental Outcome after Hematopoietic Cell Transplantation in Inborn Errors of Metabolism: Current Considerations and Future Perspectives.1 passage
• Neurodevelopmental Profile in Children Affected by Ocular Albinism.1 passage
• Neuroimaging Spectrum of Inherited Neurotransmitter Disorders.1 passage
• Neuroimaging Spectrum of Severe Hypernatremia in Infants with Neurological Manifestations.1 passage
• Neurologic Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: Aicardi-Goutières Syndrome and Beyond.1 passage
• Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey.1 passage
• Neurological Manifestations of Mycoplasma pneumoniae Infection in Hospitalized Children and Their Long-Term Follow-Up.1 passage
• Neurological Sequelae due to Inborn Metabolic Diseases in Pediatric Refugees: Challenges in Treating the Untreated.1 passage
• Neuromuscular Involvement in Glycogen Storage Disease Type III in Fifty Tunisian Patients: Phenotype and Natural History in Young Patients.1 passage
• Neuropsychological Phenotypes of Pediatric Anti-Myelin Oligodendrocyte Glycoprotein Associated Disorders: A Case Series.1 passage
• Neurovisual Assessment in Children with Ataxia Telangiectasia.1 passage
• Nevus Anemicus As an Additional Diagnostic Marker of Neurofibromatosis Type 1 in Childhood.1 passage
• Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters.1 passage
• Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients.1 passage
• Novel Mutation in ATP6V1A Gene with Infantile Spasms in an Indian Boy.1 passage
• Novel Mutation in the DKC1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome As a Rare Differential Diagnosis in Pontocerebellar Hypoplasia, Primary Microcephaly, and Progressive Bone Marrow Failure.1 passage
• Novel Mutations in the Nonselective Sodium Leak Channel (NALCN) Lead to Distal Arthrogryposis with Increased Muscle Tone.1 passage
• Novel RRM2B Mutation and Severe Mitochondrial DNA Depletion: Report of 2 Cases and Review of the Literature.1 passage
• Novel STAC3 Mutations in the First Non-Amerindian Patient with Native American Myopathy.1 passage
• Older Patients May Have More Frequent Seizures among Children Diagnosed as Benign Convulsions with Mild Gastroenteritis.1 passage
• Opening New Horizons in the Treatment of Childhood Onset Leukodystrophies.1 passage
• Optic Atrophy and Generalized Chorea in a Patient Harboring an OPA10/RTN4IP1 Pathogenic Variant.1 passage
• Optic Neuropathy, Secondary to Ethmoiditis, and Onodi Cell Inflammation during Childhood: A Case Report and Review of the Literature.1 passage
• Optimizing Detection Rate and Characterization of Subtle Paroxysmal Neonatal Abnormal Facial Movements with Multi-Camera Video-Electroencephalogram Recordings.1 passage
• Osteoid Osteoma of the Atlas in a Boy: Clinical and Imaging Features-A Case Report and Review of the Literature.1 passage
• Outbreak of Enterovirus Infection with Neurological Presentations in a Pediatric Population in Northern Spain: A Clinical Observational Study.1 passage
• Outcome of Nonketotic Hyperglycinemia in Lebanon: 14-Year Retrospective Review.1 passage
• Overlap phenotype between CMT1A and hereditary neuropathy with liability to pressure palsies caused by the novel small in-frame deletion c.407_418del12 in PMP22 gene.1 passage
• POLR3A and POLR3B Mutations in Unclassified Hypomyelination.1 passage
• PPP2R5D-Related Neurodevelopmental Disorder or Developmental and Epileptic Encephalopathy?: A Novel Phenotypic Description and Review of Published Cases.1 passage
• PRUNE1 Deficiency: Expanding the Clinical and Genetic Spectrum.1 passage
• Paroxysmal Dyskinesias Revealing 3-Hydroxy-Isobutyryl-CoA Hydrolase (HIBCH) Deficiency.1 passage
• Pediatric Headache and Epilepsy Comorbidity in the Pragmatic Clinical Setting.1 passage
• Pediatric Klüver-Bucy Syndrome: Report of Two Cases and Review of the Literature.1 passage
• Pediatric neurocysticercosis: three cases presented in the Netherlands with divergent clinical presentations.1 passage
• Percutaneous Endoscopic Gastrostomy Feeding in Children with Cerebral Palsy.1 passage
• Phase Contrast MRI Suggests an Internal Carotid Vascular Tone Alteration in Migraines.1 passage
• Phenobarbital for Neonatal Seizures: Response Rate and Predictors of Refractoriness.1 passage
• Phenotype-Genotype Correlation in Children with Neurofibromatosis Type 1.1 passage
• Phenotypic and Genotypic Heterogeneity of RRM2B Variants.1 passage
• Plasma Exchange and Immunoadsorption in Pediatric Inflammatory Optic Neuropathy Resistant to Corticosteroid Therapy: Four French Cases.1 passage
• Plasticity during Early Brain Development Is Determined by Ontogenetic Potential.1 passage
• Poland Syndrome with Atypical Malformations Associated to a de novo 1.5 Mb Xp22.31 Duplication.1 passage
• Polymorphisms of Immunoglobulin G Fc Receptors in Pediatric Guillain-Barré Syndrome.1 passage
• Possible Role of High-Dose Barbiturates and Early Administration of Parenteral Ketogenic Diet for Reducing Development of Chronic Epilepsy in Febrile Infection-Related Epilepsy Syndrome: A Case Report.1 passage
• Postherpetic Anti-N-methyl-D-aspartate Receptor Encephalitis after Hemispherotomy in a Patient with Intractable Startle Epilepsy.1 passage
• Postnatal Brain Growth Patterns in Pontocerebellar Hypoplasia.1 passage
• Postnatal Paraclinical Parameters Associated to Occurrence of Intracerebral Hemorrhage in Preterm Infants.1 passage
• Posttraumatic Delayed Jugular Foramen Syndrome in a Toddler.1 passage
• Potential Risk Factors for Autism in Children Requiring Neonatal Intensive Care Unit.1 passage
• Potential Risk Factors for Ventriculoperitoneal Shunt Implantation in Paediatric Patients with Posthemorrhagic Hydrocephalus of Prematurity Treated with Subcutaneous Reservoir: An Institutional Experience.1 passage
• Pott's Disease: An Emerging Source of Potentially Inappropriate Treatment.1 passage
• Practical Recommendations for Robot-Assisted Treadmill Therapy (Lokomat) in Children with Cerebral Palsy: Indications, Goal Setting, and Clinical Implementation within the WHO-ICF Framework.1 passage
• PredictMed: A Machine Learning Model for Identifying Risk Factors of Neuromuscular Hip Dysplasia: A Multicenter Descriptive Study.1 passage
• Prenatal Magnetic Resonance Imaging of Atypical Partial Rhombencephalosynapsis with Involvement of the Anterior Vermis: Two Case Reports.1 passage
• Prevalence of Febrile Seizures, Epilepsy, and Other Paroxysmal Attacks in a Swedish Cohort of 4-Year-Old Children.1 passage
• Prognostic value of continuous electroencephalography monitoring in children with severe brain damage.1 passage
• Progress in Neonatal Neurology with a Focus on Neuroimaging in the Preterm Infant.1 passage
• Progressive Clinical and Neuroradiological Findings in a Child with BCL11B Missense Mutation: Expanding the Phenotypic Spectrum of Related Disorder.1 passage
• Progressive Leukodystrophy-Like Demyelinating Syndromes with MOG-Antibodies in Children: A Rare Under-Recognized Phenotype.1 passage
• Pyruvate Carboxylase Deficiency Type C: A Rare Cause of Acute Transient Flaccid Paralysis with Ketoacidosis.1 passage
• Quality of Life and Fitness in Children and Adolescents with Epilepsy (EpiFit).1 passage
• Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency.1 passage
• Rate of Anti-NMDA Receptor Encephalitis in Ovarian Teratomas.1 passage
• Recent Advances in the Diagnosis and Treatment of Neonatal Seizures.1 passage
• Recurrence of Epileptic Spasms as Reflex Seizures Induced by Eating: A Case Report and Literature Review.1 passage
• Recurrent Demyelinating Episodes as Sole Manifestation of Inherited CD59 Deficiency.1 passage
• Recurrent Dystonic Crisis and Rhabdomyolysis Treated with Dantrolene in Two Patients with Aromatic L-Amino Acid Decarboxylase Deficiency.1 passage
• Recurrent Myalgia since Early Infancy-Misleading Clinical Course in a Child with Carnitine Palmitoyltransferase-II Deficiency.1 passage
• Reflex Epilepsy with Hot Water: Clinical and EEG Findings, Treatment, and Prognosis in Childhood.1 passage
• Relapse and metastasis of atypical teratoid/rhabdoid tumor in a boy with neurofibromatosis type 1 treated with recombinant human growth hormone.1 passage
• Relationship between Sedative Antihistamines and the Duration of Febrile Seizures.1 passage
• Respiratory Muscle Weakness and Respiratory Failure in Pediatric Neuromuscular Disorders: The Value of Noninvasive Determined Tension-Time Index.1 passage
• Reversible Hypertensive Myelopathy-The Spinal Cord Variant of Posterior Reversible Encephalopathy Syndrome.1 passage
• Riboflavin-Responsive Multiple Acyl-CoA Dehydrogenase Deficiency Associated with Hepatoencephalomyopathy and White Matter Signal Abnormalities on Brain MRI.1 passage
• Risk Factors for Dystonia after Selective Dorsal Rhizotomy in Nonwalking Children and Adolescents with Bilateral Spasticity.1 passage
• Risk Factors for Mortality among Newborns with Neonatal Seizures.1 passage
• Rituximab, IVIg, and Tetracosactide (ACTH1-24) Combination Immunotherapy ("RITE-CI") for Pediatric Opsoclonus-Myoclonus Syndrome: Immunomarkers and Clinical Observations.1 passage
• Role and Clinical Significance of Plasma N-Terminal Brain Natriuretic Peptide Measurement in Children with Brain Edema.1 passage
• Rotavirus-Induced Neonatal Epileptic Encephalopathy-A Disease Spectrum Illustrated by Monochorionic Twins.1 passage
• SLC19A3 Gene Defects Sorting the Phenotype and Acronyms: Review.1 passage
• SLC7A3: In Silico Prediction of a Potential New Cause of Childhood Epilepsy.1 passage
• SYNGAP1 Mutation in Focal and Generalized Epilepsy: A Literature Overview and A Case Report with Special Aspects of the EEG.1 passage
• Saposin B-Deficient Metachromatic Leukodystrophy Mimicking Acute Flaccid Paralysis.1 passage
• School-Age Outcome of Fetuses with Isolated Complete Septum Pellucidum Agenesis at Prenatal Magnetic Resonance Imaging.1 passage
• Secondary Bone Defect in Neuromuscular Diseases in Childhood: A Longitudinal "Muscle-Bone Unit" Analysis.1 passage
• Seizure Freedom in Patients with Dravet Syndrome with Contraceptives: A Case Report with Two Patients.1 passage
• Severe Hypertriglyceridemia in Glut1D on Ketogenic Diet.1 passage
• Severe Locked-In-Like Guillain-Barré's Syndrome: Dilemmas in Diagnosis and Treatment.1 passage
• Severe Metabolic Acidosis and Hepatopathy due to Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate.1 passage
• Severe and Progressive Fetal Ventriculomegaly Leading to the Diagnosis of Periventricular Nodular Heterotopias with Good Outcome.1 passage
• Severity of Cerebral Palsy-The Impact of Associated Impairments.1 passage
• Should Posterior Reversible Encephalopathy Syndrome Be Mainly Considered an Epileptic Disorder? Results of a Sequential Neurophysiological Study in a Pediatric Cohort.1 passage
• Shunt Dependency Syndrome after Cyst-Peritoneal Shunt Resolved by Keyhole Microsurgical Cyst Resection: Two Case Reports and Literature Review.1 passage
• Single-Photon Emission Computed Tomography Is an Ambiguous Imaging Method on Initial Diagnosis for Acute Encephalopathy.1 passage
• Sleep Disorder: An Overlooked Manifestation of Glucose Transporter Type-1 Deficiency Syndrome.1 passage
• Sleep Disturbances in Children with Rolandic Epilepsy.1 passage
• Sleep Quality in Children and Adults with Rett Syndrome.1 passage
• Sleep and epilepsy syndromes.1 passage
• Sleep in children with neurodevelopmental disabilities.1 passage
• Spasmodic Abdominal Pain and Other Gastrointestinal Symptoms in Pontocerebellar Hypoplasia Type 2.1 passage
• Specific Cognitive Changes due to Hippocalcin Alterations? A Novel Familial Homozygous Hippocalcin Variant Associated with Inherited Dystonia and Altered Cognition.1 passage
• Spinal Nerve Roots Abnormalities on MRI in a Child with SURF1 Mitochondrial Disease.1 passage
• Stability of 0.5% Glucose-Containing Balanced Electrolyte Solutions for Patients on Ketogenic Diets: A Laboratory Study.1 passage
• Static Leukoencephalopathy Associated with 17p13.3 Microdeletion Syndrome: A Case Report.1 passage
• Stroke as Initial Manifestation of Adenosine Deaminase 2 Deficiency.1 passage
• Stylohyoid Complex (Eagle) Syndrome Starting in a 9-Year-Old Boy.1 passage
• Subdural Hygroma in an Infant with Marfan's Syndrome.1 passage
• Surgical Treatment and Long-Term Outcome of Cerebral Cavernous Malformations-Related Epilepsy in Pediatric Patients.1 passage
• Susceptibility-Weighted Magnetic Resonance Imaging Findings of Two Pediatric Migraine Patients with Aura.1 passage
• Symmetrical Thalamic Lesions in the Newborn: A Case Series.1 passage
• TSC1 as a Novel Gene for Sleep-Related Hypermotor Epilepsy: A Child with a Mild Phenotype of Tuberous Sclerosis.1 passage
• Testosterone Treatment of Pubertal Delay in Duchenne Muscular Dystrophy.1 passage
• The "Ivy-Sign" in Moyamoya Disease-From MRI Pattern to Diagnosis.1 passage
• The Cerebellum and Its Wrapping Meninge: Developmental Interplay between Two Major Structures.1 passage
• The Changing Landscape of Pediatric Low-Grade Gliomas: Clinical Challenges and Emerging Therapies.1 passage
• The Clinical Picture of a Bilateral Perisylvian Syndrome as the Initial Symptom of Mega-Corpus-Callosum Syndrome due to a MAST1-Gene Mutation.1 passage
• The Complexity Signature: Developing a Tool to Communicate Biopsychosocial Severity of Disease for Children with Chronic Neurological Complexity.1 passage
• The Direct Costs of Dravet's Syndrome before and after Diagnosis Assessment.1 passage
• The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other Neurological Disorders in Classical Phenotype of Glucose Transporter 1 Deficiency Syndrome.1 passage
• The Impact of 3:1 Ketogenic Diet on Cardiac Repolarization Changes in Children with Refractory Seizures: A Prospective Follow-Up Study.1 passage
• The Involvement of Speed-of-Processing in Story Listening in Preschool Children: A Functional and Structural Connectivity Study.1 passage
• The Ketogenic Diet and Its Effect on Bone Mineral Density: A Retrospective Observational Cohort Study.1 passage
• The Largest Germline Heterozygous Deletion Encompassing Potocki-Shaffer and WAGR Syndromes Loci to Date: A Case Report.1 passage
• The Origin of the Cerebral Palsies: Contribution of Population-Based Neuroimaging Data.1 passage
• The Persistent Generalized Muscle Contraction in Siblings with Molybdenum Cofactor Deficiency Type A.1 passage
• The Variable Expression of a Novel MBD5 Gene Frameshift Mutation in an Italian Family.1 passage
• The juvenile head trauma syndrome: a trauma triggered migraine?1 passage
• The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBS.1 passage
• Thiamine Pyrophosphokinase Deficiency due to Mutations in the TPK1 Gene: A Rare, Treatable Neurodegenerative Disorder.1 passage
• Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 Variants.1 passage
• Three Individuals with PURA Syndrome in a Cohort of Patients with Neuromuscular Disease.1 passage
• Tic Disorders and Tourette Syndrome: Current Concepts of Etiology and Treatment in Children and Adolescents.1 passage
• Tolosa-Hunt Syndrome in Childhood and Adolescence: A Literature Review in the Last 10 Years.1 passage
• Tone Reduction and Physical Therapy: Strengthening Partners in Treatment of Children with Spastic Cerebral Palsy.1 passage
• Tonic Seizure Status Epilepticus Triggered by Valproate in a Child with Doose Syndrome.1 passage
• Tonic Tics in Gilles de la Tourette Syndrome.1 passage
• Trametinib Induces Neurofibroma Shrinkage and Enables Surgery.1 passage
• Transtemporal Ultrasound (US) Assessment of Third Ventricle Diameter (TVD): Comparison of US and MRI TVD in Pediatric Patients.1 passage
• Treatment of Infantile Spasms: Report of the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society for Neuropediatrics.1 passage
• Tuberous Sclerosis Complex Associated Neuropsychiatric Disorders and Parental Stress: Findings from a National, Prospective TSC Surveillance Study.1 passage
• Two Cases of Pediatric AQP4-Antibody Positive Neuromyelitis Optica Spectrum Disorder Successfully Treated with Tocilizumab.1 passage
• UBTF Mutation Causes Complex Phenotype of Neurodegeneration and Severe Epilepsy in Childhood.1 passage
• Unilateral Hearing Loss Due to Cochlear Nerve Involvement as Isolated Symptom of a Primary Medulloblastoma.1 passage
• Unresponsive Wakefulness Syndrome in Children after Near-Drowning: Long-Term Outcome and Impact on the Families.1 passage
• Use of Levetiracetam in Neonates in Clinical Practice: A Retrospective Study at a German University Hospital.1 passage
• Use of Perampanel and a Ketogenic Diet in Nonketotic Hyperglycinemia: A Case Report.1 passage
• Using Artificial Intelligence to Identify Factors Associated with Autism Spectrum Disorder in Adolescents with Cerebral Palsy.1 passage
• Utility of Epilepsy Surgery in Survivors of Childhood Cancer.1 passage
• Variable Genotype-Phenotype Correlation of Pompe's Disease Caused by a c.2015 G > A (p.Arg672Gln) Mutation in the GAA Gene.1 passage
• Variants in the ATP1A3 Gene Mutations within Severe Apnea Starting in Early Infancy: An Observational Study of Two Cases with a Possible Relation to Epileptic Activity.1 passage
• Ventricular Catheter Systems with Subcutaneous Reservoirs (Ommaya Reservoirs) in Pediatric Patients with Brain Tumors: Infections and Other Complications.1 passage
• Vestibular Migraine with Visual Aura and Olfactory Hallucination in Children: Two Case Reports.1 passage
• Vitamin B12 Deficiency and West Syndrome: An Uncommon but Preventable Cause of Neurological Disorder. Report on Three Cases, One of Them with Late Onset during Vitamin B12 Treatment.1 passage
• Vitamin B6-Responsive Epilepsy due to a Novel KCNQ2 Mutation.1 passage
• Wallenberg Syndrome: An Exceptional Cause of Acute Vertigo in Children.1 passage
• Whole Exon Deletion in the GFAP Gene Is a Novel Molecular Mechanism Causing Alexander Disease.1 passage
• Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy.1 passage
• X-Linked Hereditary Motor Sensory Neuropathy Type 1 (CMTX1) in a Three-Generation Gelao Chinese Family.1 passage
• X-linked Charcot-Marie-Tooth Disease Presenting with Stuttering Stroke-like Symptoms.1 passage
• Xp11.22 Microduplications Including HUWE1: Case Report and Literature Review.1 passage
• Yield of Brain Magnetic Resonance Imaging in Epilepsy Diagnosis from 1998 to 2020: A Large Retrospective Cohort Study.1 passage
• Young Adult Motor, Sensory, and Cognitive Outcomes and Longitudinal Development after Very and Extremely Preterm Birth.1 passage