Results 131 to 140 of about 268,123 (292)

Short-Duration ACTH Therapy for West Syndrome

, 2006
Short-term developmental and seizure outcomes were assessed in 7 children, aged
J Gordon Millichap
core   +1 more source

Insights into ANKRD11‐related epilepsy from 163 people

Epilepsia, EarlyView.
Abstract Objective Ankyrin repeat domain 11 gene (ANKRD11) is the key disease gene for autosomal dominant KBG syndrome, and a subset of affected individuals develop epilepsy. However, comprehensive characterization of epilepsy‐related phenotypes and genotype–phenotype correlations in ANKRD11 variant carriers remains limited.
Song Su, Jian Ma, Qi Zhang, Wandong Hu, Ying Ren, Wenchao Zhang, Hongwei Zhang   +6 more
wiley   +1 more source

COVID-19 in Children with West Syndrome: An Ambispective Study. [PDF]

Indian J Pediatr, 2023
Madaan P, Saini L, Dhir P, Vikas S, Bhagwat C, Goel M, Soni A, Sahu JK.   +7 more
europepmc   +1 more source

West syndrome associated with Down syndrome: Case report and literature review

, 2014
West syndrome is the most frequent cause of epilepsy in Down syndrome. West syndrome is often associated with poor long-term prognosis in most of children.
Ghanmi, Sobhi, Sfar, Mohamed Tahar, Ben Hamouda, Hechmi, Mnasri, Hanen, Sakli, Gazi, Dogui, Mohamed, Soua, Habib   +6 more
core   +1 more source

Epilepsy syndromes classification

Epilepsia Open, EarlyView.
Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell, Nicola Specchio, Rima Nabbout, Phillip L. Pearl, Kate Riney   +4 more
wiley   +1 more source

Adrenocorticotropic Hormone Induced Status Dystonicus in a Child with West Syndrome. [PDF]

Indian J Crit Care Med, 2022
Singh J, Aulakh R.
europepmc   +1 more source

3-Phosphoglycerate dehydrogenase deficiency in a patient with West syndrome

, 2000
3-phosphoglycerate dehydrogenase deficiency is a severe but treatable disorder of serine synthesis, first described in 1996 (Jaeken et al. 1996a).
Sau, I, Santos, S, Jaeken, J, Vilaseca, M.A., Garcia-Gonzalez, M.M., Artuch, S, Aracil, A, Van Schaftingen, Emile, Pineda, M   +8 more
core   +1 more source

Frontiers in EEG as a tool for the management of pediatric epilepsy: Past, present, and future

Epilepsia Open, EarlyView.
Abstract Electroencephalography (EEG) has evolved into an indispensable tool in pediatric epilepsy, fundamentally transforming the diagnosis, classification, and management of this condition. This review chronicles the historical journey of EEG from its groundbreaking inception to its current pivotal role in delineating distinct pediatric epilepsy ...
Hiroki Nariai
wiley   +1 more source

Disparities in the utilization of genetic testing for non‐acquired infantile epileptic spasms syndrome in a single healthcare center in North Carolina

Epilepsia Open
Objective To investigate disparities in the utilization of genetic sequencing among children with Infantile Epileptic Spasms Syndrome (IESS), a severe early‐onset epilepsy where timely diagnosis and treatment are crucial for improving neurodevelopmental ...
Kenza El Marzouki, Bridley K. Jenkins, Tamy Moraes Tsujimoto, Huijun Jiang, Emma B. Cardwell, Martin Arhin, Unwana Eyo, Cristian Gonzalez‐Rodriguez, Stephanie Peck, Feng‐Chang Lin, Senyene E. Hunter   +10 more
doaj   +1 more source

West Syndrome and the Importance of Routine Physical Examinations and Parental Education: A Case Report. [PDF]

Cureus, 2022
Dias Freitas F, Cavaco Raposo S, Luis Nogueira A.   +2 more
europepmc   +1 more source