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Two Siblings Showing a Mild Phenotype of Joubert Syndrome with a Specific CEP290 Variant

期刊: NEUROPEDIATRICS, 2023; 54 (3)

Joubert syndrome (JS) is a genetic neurodevelopmental disorder characterized by lower brainstem dysplasia and cerebellar vermis agenesis termed molar ......

Acute Corticosteroid Responsive Meningoencephalitis with Cerebral Vasculitis after COVID-19 Infection in a Thirteen-Year-Old Case Report

期刊: NEUROPEDIATRICS, 2023; 54 (1)

Introduction Various neurologic manifestations have already been described in children during or after severe acute respiratory syndrome coronavirus 2......

Efficacy of Melatonin for Insomnia in Children with Autism Spectrum Disorder: A Meta-analysis

期刊: NEUROPEDIATRICS, 2023; 54 (3)

Aim This study aimed to evaluate the effectiveness of melatonin in treating insomnia in children with autism spectrum disorder (ASD).Methods Comprehen......

The Coexistence of Two Genetic Astrocytopathies-Megalencephalic Leukoencephalopathy and Vanishing White Matter Disease-in an Indian Child

期刊: NEUROPEDIATRICS, 2023; 54 (2)

A 9-month-old male child, born of second-degree consanguinity, presented with a progressively enlarging head since early infancy. The child had normal......

Ketogenic Diet in Neonates with Drug-Resistant Epilepsy: Efficacy and Side Effects-A Single Center's Initial Experience

期刊: NEUROPEDIATRICS, 2023; 54 (5)

Background For patients with pharmacoresistant epilepsy, a therapeutic option is ketogenic diet. Currently, data on young infants are scarce, particul......

Electroclinical Features of Epilepsy in Kleefstra's Syndrome

期刊: NEUROPEDIATRICS, 2023; 54 (6)

Background Kleefstra's syndrome (KS) or 9q34.3 microdeletion syndrome (OMIM #610253) is a rare genetic condition featuring intellectual disability, hy......

Effectiveness of Neuropediatric Inpatient Rehabilitation

期刊: NEUROPEDIATRICS, 2023; ()

Aim Inpatient rehabilitation plays an important role in treating neurological diseases in children and adolescents. However, there is a lack of curren......

Clinical Course May Be Independent from Neuroimaging in DEPDC-5-Related Epilepsy

期刊: NEUROPEDIATRICS, 2023; 54 (5)

DEPDC5 is an upstream repressor of the mechanistic target of rapamycin pathway via the GATOR-1 complex. Pathogenic variants causing loss of function t......

Cognitive and Brain Gray Matter Changes in Children with Obstructive Sleep Apnea: A Voxel-Based Morphological Study

期刊: NEUROPEDIATRICS, 2023; 54 (2)

Background To explore the neural difference between children with obstructive sleep apnea (OSA) and healthy controls, together with the relation betwe......

Evidence for a Pathogenic Role of CSMD1 in Childhood Apraxia of Speech

期刊: NEUROPEDIATRICS, 2023; 54 (6)

Childhood apraxia of speech (CAS) is a pediatric motor speech disorder. The genetic etiology of this complex neurological condition is not yet well un......

Effects of Sodium Lactate Infusion in Two Girls with Glucose Transporter 1 Deficiency Syndrome

期刊: NEUROPEDIATRICS, 2023; 54 (6)

Background Glucose is an important fuel for the brain. In glucose transporter 1 deficiency syndrome (GLUT1DS), the transport of glucose across the blo......

Impact of Tourette Syndrome on Education

期刊: NEUROPEDIATRICS, 2023; 54 (2)

Background Previous studies have shown that Tourette syndrome (TS) has an impact on academic achievements. The aim of this study was to investigate th......

Kidney Stones in Epileptic Children Receiving Ketogenic Diet: Frequency and Risk Factors

期刊: NEUROPEDIATRICS, 2023; 54 (5)

Background Although it is a valuable option for children with drug-resistant epilepsy, ketogenic diet (KD) therapy is associated with several side eff......

Observation of a Possible Successful Treatment of DEPDC5 -Related Epilepsy with mTOR Inhibitor

期刊: NEUROPEDIATRICS, 2023; 54 (5)

The mechanistic target of the rapamycin signaling pathway serves as a central regulator of cell metabolism, growth, proliferation, and survival. In it......

Claude Syndrome in Childhood Associated with Probable Neuro-Behcet Disease

期刊: NEUROPEDIATRICS, 2023; 54 (1)

Claude syndrome is a rare midbrain stroke syndrome characterized by ipsilateral third cranial nerve palsy and contralateral hemiataxia. So far, only a......

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