Results 61 to 70 of about 2,875,412 (170)

Electrophysiological study of peripheral nerves in children with acute lymphoblastic leukemia

Egyptian Rheumatology and Rehabilitation, 2013
findings predominantly the hypsarrhyth-mia or modified hypsarrhythmia are the hallmark. Majority of children received conventional AED with poor response. Oral prednisolone is proved to be the most effective AED.
Ibrahim K. Ibrahim, Hoda A Hassab, Mohamed H. Imam, Hayam M. Abd El Ghany, Kareem A. Omar   +4 more
semanticscholar   +1 more source

Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature

Epileptic Disorders, Volume 27, Issue 5, Page 745-802, October 2025.
Abstract Although inborn errors of metabolism (IEM) are a rare cause of epilepsy, seizures are a common presentation in these disorders. Seizures in IEM are frequently refractory to conventional anti‐seizure medication and might warrant initiation of specific treatments based on vitamins or dietary modifications or provision of alternative substrates ...
D. Kapoor, S. Sharma, A. Kaminska, R. Nabbout, N. Chemaly, M. Schiff, P. De Lonlay, M. Eisermann   +7 more
wiley   +1 more source

Pattern of EEG Change in Infants with West Syndrome: A Retrospective Study

, 2018
West syndrome (WS) is a severe form of epilepsy of early infancy. Its diagnosis, evaluation, and management continue to pose many challenges to health care professionals and affected families. Methodology: It is a retrospective review of patients of West
K. Fatema, Mizanur Rahman, S. Akhter, T. Saad, Suraiya Begum, Naznin Akter   +5 more
semanticscholar   +1 more source

Cannabidiol attenuates epileptic phenotype and increases survival in a mouse model of developmental and epileptic encephalopathy type 1

Epilepsia, Volume 66, Issue 10, Page 4035-4052, October 2025.
Abstract Objective Developmental and epileptic encephalopathy type 1 (DEE1) is a rare drug‐resistant pediatric epilepsy caused by trinucleotide repeat expansions in the X‐linked ARX gene, leading to elongation of the first polyalanine tract. It presents with early onset tonic seizures or spasms, developmental and cognition delay, and high risk of ...
Lucia Verrillo, Fabio Arturo Iannotti, Denise Drongitis, Katiuscia Martinello, Loredana Poeta, Adriano Barra, Gaetano Terrone, Sergio Fucile, Vincenzo Di Marzo, Maria Giuseppina Miano   +9 more
wiley   +1 more source

Response to treatment in a prospective national infantile spasms cohort [PDF]

, 2016
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/134499/1/ana24594.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/134499/2/ana24594_am ...
Adam L. Hartman, Anne T. Berg, Dennis Dlugos, Douglas R. Nordli, Elaine Wirrell, Eric H. Kossoff, Erin Leister, Jason Coryell, John Millichap, John R. Mytinger, Joseph Sullivan, Katherine C. Nickels, Kelly G. Knupp, Lorie Hamikawa, Nicole Ryan, null null, Renée A. Shellhaas, Sucheta Joshi, Tobias Loddenkemper, William D. Gaillard, Zachary Grinspan   +20 more
core   +1 more source

A companion to the preclinical common data elements for rodent models of pediatric acquired epilepsy: A report of the TASK3‐WG1B, Pediatric and Genetic Models Working Group of the ILAE/AES Joint Translational Task Force

Epilepsia Open, Volume 10, Issue S1, Page S53-S86, August 2025.
Abstract Epilepsy syndromes during the early years of life may be attributed to an acquired insult, such as hypoxic–ischemic injury, infection, status epilepticus, or brain trauma. These conditions are frequently modeled in experimental rodents to delineate mechanisms of epileptogenesis and investigate novel therapeutic strategies.
Anna‐Maria Katsarou, Hana Kubova, Stéphane Auvin, Massimo Mantegazza, Melissa Barker‐Haliski, Aristea S. Galanopoulou, Christopher A. Reid, Bridgette D. Semple   +7 more
wiley   +1 more source

Electroencephalographic characterization of a case of infantile spasm with atypical presentation [PDF]

Infantile spasm is one of the common seizure disorders with serious consequences. It is generally characterized by a muscle spasm of various intensity and distribution, salaam spells, and infantile myoclonic seizures with typical electroencephalography ...
Jha, Kamlesh, Kumar, Tribhuwan, Kumar, Yogesh, Mishra, Abhilasha, Singh, Ramji   +4 more
core   +2 more sources

Electro-clinical and neurodevelopmental outcome in six children with early diagnosis of tuberous sclerosis complex and role of the genetic background [PDF]

, 2020
Background: Seizures in individuals affected by tuberous sclerosis complex (TSC) commonly develop in the first year of life, are often preceded by a progressive deterioration of the electroencephalogram (EEG), and likely influence developmental outcome ...
A. Mingarelli, A. Peron, A. Vignoli, F. Cervi, F. La Briola, M.N. Savini, M.P. Canevini, R.M. Alfano   +7 more
core   +1 more source

Efficacy and tolerability of perampanel as add‐on therapy in Dravet syndrome: A prospective real‐world study

Epilepsia Open, Volume 10, Issue 4, Page 1043-1053, August 2025.
Abstract Objective To investigate the efficacy and tolerability of perampanel (PER) on Dravet syndrome in China by a prospective real‐world study. Methods We prospectively enrolled children with Dravet syndrome from the neurology clinic of Shenzhen Children's Hospital from September 2020 to October 2021.
Han Wang, Hong Chen, Xin Ding, Xueyan Cao, Jiahui Mai, Huafang Zou, Dongfang Zou, Yanwei Zhu, Jianxiang Liao, Dezhi Cao   +9 more
wiley   +1 more source

Aetiopathogenesis of infantile epileptic spasms syndrome and mechanisms of action of adrenocorticotrophin hormone/corticosteroids in children: A scoping review

Developmental Medicine &Child Neurology, Volume 67, Issue 8, Page 1004-1025, August 2025.
Why does infantile epileptic spasms syndrome (IESS) occur with a variety of underlying conditions and why does it respond to adrenocorticotrophin hormone (ACTH)/corticosteroids? Our scoping review summarizes five hypotheses from the literature: gene/epigenetic regulation, stress/HPA axis activation, neuroinflammation/immune function, altered neuronal ...
Emily A. Innes, Velda X. Han, Shrujna Patel, Michelle A. Farrar, Deepak Gill, Shekeeb S. Mohammad, Russell C. Dale   +6 more
wiley   +1 more source