ICV Value = 85.33
ISSN: 2642-4797
Journal of Pediatric Neurology and Neuroscience is an open access, peer reviewed journal international peer review journal covering the latest advances in clinical practice and research in the diagnosis, management, and treatment of pediatric neurologic disorders. The journal strive to gather articles focusing most up-to-date and highest quality care for children with a wide range of neurological disorders. The section editors lead the journal's published content after close evaluation and selection of the high quality articles ensuring the most authoritative and extensive coverage of the field with originality and advancement in clinical practice.
Citing the work will allow the readers to freely use and re use the information under the terms of Creative Commons Attribution License. The journal encourages authors to contribute in wide range of formats such as original articles, review articles, short reports, rapid communication, commentaries, case series, case reports, clinical images, letter to editors.
The journal features bringing up to date information on the latest advances in the diagnosis, management, and treatment of pediatric neurologic disorders.
Neurologist
Massachusetts General Hospital
Boston
United States of America
Tel: 617-724-7426
Professor
Department of Behavioral Neurosciences & Psychology
California Institute of Behavioral Neurosciences & Psychology
California
United States of America
Professor
Molecular medicine department
Laval University
Canada
Tel: +1 418-525-4444
Professor
Department of Psychology
University of Gothenburg
Sweden
Tel: +46-31-786-4694
Medical Director
The Neonatal Intensive Care Unit
The University Hospital of Siena
Italy
Tel: 0039-347-357-4566
Director of Center for rare genetic diseases
Villa Sofia-Cervello Hospital
University of Palermo
Palermo
Italy
Submit your manuscript to this journal through online or email us at editorialoffice@scholars.direct
Case Report
Concurrent Guillain-Barré Syndrome and Thoracic Syringomyelia in a Pediatric Patient: A Case Report
Guillain-Barré Syndrome (GBS) is an acute immune-mediated polyneuropathy characterized by ascending weakness, areflexia, and risk of respiratory ... Read more
Case Review
Metabolic Dysfunction in Shashi-Pena Syndrome: A Novel Pathologic ASXL2 Frameshift Variant
ASXL2 is a member of the Additional sex combs (Asx)-like gene family, essential for embryonic development and homeostasis. Germline truncating variant... Read more
Review Article
Valproate, recognized as a broad-spectrum antiepileptic agent, is extensively employed in the treatment of epilepsy, as well as a range of neuropsycho... Read more
Case Report
Neonatal seizures, particularly refractory status epilepticus (RSE), pose significant challenges in neonatal intensive care units (NICUs), especially ... Read more
Review Article
Supporting Autonomy for Patients with Intellectual Disability: Principles for Care Providers
Individuals experiencing intellectual disabilities (ID) often experience restricted autonomy. The prima facie core ethical principle of autonomy provi... Read more
Review Article
Pediatric NMDA Receptor Encephalitis: A Case of Speech Regression and Behavioral Changes
Anti-N-methyl-D-asparate receptor (NMDA) receptor encephalitis is a rare autoimmune disorder (estimated prevalence is 1-2 in a million) characterized ... Read more
Review Article
Periosinus Abscess Mimicking Sinus Vein Thrombosis
Sigmoid sinus vein thrombosis is a rare but life-threatening complication of acute otitis media and mastoiditis. In this case, a 7-years-old male pati... Read more
Review Article
Dias-Logan syndrome, also known as BCL11A- related intellectual disability, is caused by pathogenic va... Read more
Review Article
Rhythmic High-Amplitude Delta with Superimposed Spikes (RHADS): A Treatment Dilemma
Rhythmic High-Amplitude Delta Activity with Superimposed (poly)spikes (RHADS) is a pathognomonic electroencephalography (EEG) signature that may facil... Read more
Case Report
Wernicke Encephalopathy in a Non-Alcoholic Obese Adolescent: A Case Report
Wernicke encephalopathy (WE) is a life-threatening condition caused by a deficiency in thiamine, also known as Vitamin B1. WE is known to occur mainly... Read more
