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
Reversible cerebral vasoconstriction syndrome (RCVS) is clinical and radiographic entity with several identified triggers, characterized by severe hea... Read more
Case Report
Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) is a rare autoimmune disorder, often of idiopathic cause, but one that can result as a compli... Read more
Case Report
Treatment of Bi-Allelic PRRT-2 Mutation Associated Ataxia and Paroxysmal Dyskinesia
PRRT2 is located on chromosome 16p11.2 and is a transmembrane protein highly expressed in the CNS that has been identified to play a role in epilepsy,... Read more
Case Report
Treatment of COVID Encephalitis in Pediatric Patient with IVIG
We herein report a case of encephalitis in a pediatric patient with SARS-COVID-19 infection. The diagnosis is discussed consisting of physical exam, e... Read more
Case Report
It's a Bit Crowded in Here: Examining Pressure Reactivity in Craniocerebral Disproportion
Pressure reactivity index (PRx) is a measure used to gain insights into cerebrovascular reactivity. It is generally used in acute settings such as tra... Read more
Case Report
A Novel PPP2CA Gene Variant Presenting with Dystonia and Progressive Brain Atrophy
PPP2CA gene mutations are rare and associated with a neurodevelopmental disorder with or without structural brain abnormalities. We present a case of ... Read more
Original Article
Focal Electrographic Hints in Epileptic Spasms
Epileptic spasms (ES) is an age specific seizure disorder which is more frequent in infancy. Frequent untreated epileptic events have negative effect ... Read more
Case Report
Transverse Myelitis Secondary to SARS-CoV-2 Infection in a Pediatric Patient
The clinical case of an 11-year-old male patients presented, treated at the Internal Medicine Service of the Hospital Regional de Alta Especialidad de... Read more
Research Article
Febrile Coronavirus and Autism
A number of reports have pointed to the apparent relationship between reduced IGF1 in pregnancies and the development of autism in the offspring. Feve... Read more
Case Report
CD59 Deficiency in Two Bahraini Children: Clinical Profile and Outcome
CD59 is an inherited autosomal recessive disorder characterized by various clinical manifestations including hemolytic anemia, neurological deficit du... Read more
