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Investigating the burden of cerebral palsy in low- and middle-income countries: Implications and priorities for pediatric neurology
Cerebral Palsy (CP) is a neurodevelopmental condition that results in varying motor impairment depending on the brain area...
Etiology and diagnosis of cerebral palsy in resource-limited regions
Cerebral palsy (CP) is the most common cause of childhood motor disability, with a global prevalence of 1.5-3 per 1000 liv...
EEG findings in Lennox-Gastaut syndrome: Pursuing a moving target
Lennox-Gastaut syndrome (LGS) is a chronic, developmental epileptic encephalopathy whose definition has evolved over time,...
Lennox-Gastaut syndrome: Progress, challenges, and future directions
Volume 56, December 2025, 101236Author links open overlay panelDebopam SamantaShow moreAccess through your organizationChe...
“William G. Lennox: A legacy of compassion and controversy”
William Gordon Lennox (1884–1960) was a pivotal figure in twentieth-century neurology whose pioneering research on electro...
Late onset Lennox-Gastaut syndrome
Lennox-Gastaut Syndrome (LGS) is one of the Developmental Epileptic Encephalopathy syndromes characterized by a triad of m...
Lennox-Gastaut syndrome: Comorbidities and clinical implications
Lennox-Gastaut syndrome (LGS) is a severe developmental and epileptic encephalopathy that typically begins in early childh...
Quality of life in individuals with Lennox-Gastaut syndrome and their families
Volume 56, December 2025, 101244Author links open overlay panelMary Wojnaroski a, Megan Votoupal b, Sandi Lam b c, Anup D....
Feasibility of sleep assessment modalities in children with Lennox-Gastaut syndrome
Volume 56, December 2025, 101241Author links open overlay panel, , , , , , , AbstractBackgroundSleep disorders in children...
Expanding the toolkit: An update on the evolution of new therapies for Lennox-Gastaut Syndrome
Lennox-Gastaut Syndrome (LGS) is a severe developmental epileptic encephalopathy (DEE) defined by drug refractory epilepsy...
Dietary therapies in Lennox-Gastaut syndrome
Lennox-Gastaut Syndrome (LGS) is a severe developmental and epileptic encephalopathy of childhood, characterized by drug-r...
Neuromodulation in Lennox-Gastaut Syndrome: Emerging therapies and future directions
Lennox-Gastaut syndrome (LGS) is a severe drug-resistant developmental and epileptic encephalopathy with slow spike and wa...
Surgical management of Lennox-Gastaut syndrome: A focused update on resective surgery and corpus callosotomy
Lennox-Gastaut Syndrome (LGS) is a severe developmental epileptic encephalopathy (DEE) with onset in childhood (under age ...
Preclinical models of Lennox-Gastaut syndrome: Progress and priorities
Lennox–Gastaut Syndrome (LGS) is a developmental and epileptic encephalopathy defined by the clinical triad of multiple se...
Pathophysiological pathways in mild traumatic brain injury
Mild traumatic brain injury (mTBI) is a disorder of physiologic dysfunction of the brain from trauma, and is the most comm...
Policy and advocacy for concussion awareness and safety
Concussion represents a growing public health concern, particularly among youth athletes. Legislative efforts across the U...
Longitudinal effects of pediatric concussion into adulthood
Available online 21 January 2026, 101259Author links open overlay panelRachael S. Mathew a, Caitlin Segura a, Abigail Lemo...
Defining concussion: Current concepts and diagnostic criteria
There are many definitions of concussion, but it is generally agreed upon that a concussion is a type of mild traumatic br...
Beyond the Grey Scale: A Focus Review of Microstructural, Metabolic, and AI-Driven Advances in TBI Neuroimaging
Traumatic Brain Injury (TBI) remains a leading cause of mortality and long-term disability worldwide, presenting a silent ...
Evidence-Based Management Strategies for Adult Concussion
Mild Traumatic Brain Injury (mTBI) also known as a concussion, is a growing public health concern. Accounting for 80-90% o...
Neurocutaneous Disorders of Childhood and Adolescence: Towards Earlier Diagnosis and Improved Treatment
Cookies are used by this site. Cookie SettingsAll content on this site: Copyright © 2025 Elsevier B.V., its licensors, an...
Review of encephalocraniocutaneous lipomatosis
Encephalocraniocutaneous lipomatosis (ECCL) is a sporadic neurocutaneous disorder first described in 1970 by Haberland and...
Ataxia telangiectasia
Volume 52, December 2024, 101169Author links open overlay panel, AbstractAtaxia telangiectasia (AT) is a rare neurocutaneo...
Chedíak-Higashi Syndrome: Hair-to-toe spectrum
Chedíak-Higashi Syndrome (CHS) is a rare autosomal recessive disorder characterized by a broad spectrum of clinical manife...
Hereditary hemorrhagic telangiectasia: A pediatric-focused review
Volume 52, December 2024, 101167Author links open overlay panel, AbstractClinical manifestations of hereditary hemorrhagic...
Neurofibromatosis type 1 - an update
Neurocutaneous disorders are characterized by a heterogeneous presentation where involvement of the skin and central nervo...
Neurofibromatosis type 2-related schwannomatosis - An update
Neurofibromatosis type 2-related schwannomatosis (NF2-SWN) is characterized by bilateral vestibular schwannomas in additio...
Foreword to pediatric CNS Tumors: Clinical presentation, management and sequalae
Cookies are used by this site. Cookie SettingsAll content on this site: Copyright © 2025 Elsevier B.V., its licensors, an...
Pediatric CNS tumors: Overview and treatment paradigms
Central nervous system (CNS) tumors represent the most common solid tumors occurring in children with an age-standardized ...
Pediatric headache attributed to brain tumor
Parents of children with new onset and/or frequent headaches are often concerned that their children may have brain tumors...
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