Results 31 to 40 of about 1,226,813 (207)

IvanSanchezFernandez/IS_temporaltrends: Temporal trends infantile spasms

, 2022
Code for the article "Temporal trends in the cost and use of first-line treatments for infantile epileptic spasms ...
IvanSanchezFernandez
core   +1 more source

Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies

Neurobiology of Disease, 2015
Early onset and infantile epileptic encephalopathies (EIEEs) are usually associated with medically intractable or difficult to treat epileptic seizures and prominent cognitive, neurodevelopmental and behavioral consequences.
Aristea S. Galanopoulou, Solomon L. Moshé   +1 more
doaj   +1 more source

Time-frequency characteristics of scalp high-frequency oscillations provide complementary biomarkers in infantile epileptic spasms syndrome. [PDF]

Exp Physiol
Abstract Infantile epileptic spasms syndrome (IESS) is characterized by epileptic spasms (ES) in infants and hypsarrhythmia on EEG. High‐frequency oscillations (HFOs), defined as oscillatory events at >80 Hz, reflect rapid spatiotemporal dynamics of cortical activity and might serve as novel biomarkers for epilepsy.
Yamaguchi S, Maeda K, Ishihara N, Furukawa G, Tsuboi H, Osakabe K, Sugimoto K, Ichino N.   +7 more
europepmc   +2 more sources

High-Dose Phenobarbital for Ohtahara Syndrome

Pediatric Neurology Briefs, 2002
Oral high-dose phenobarbital therapy was effective in the control of tonic spasms in a 1 month-old-infant with early infantile epileptic encephalopathy with suppression bursts (Ohtahara syndrome) treated at Tokyo Metropolitan Hachioji Children’s Hospital,
J Gordon Millichap
doaj   +1 more source

Current understanding and neurobiology of epileptic encephalopathies

Neurobiology of Disease, 2016
Epileptic encephalopathies are a group of diseases in which epileptic activity itself contributes to severe cognitive and behavioral impairments above and beyond what might be expected from the underlying pathology alone.
Stéphane Auvin, Maria Roberta Cilio, Annamaria Vezzani   +2 more
doaj   +1 more source

Infantile spasms and developmental delay: A case of miller–Dieker syndrome

Indian Pediatrics Case Reports, 2023
Background: Miller–Dieker syndrome (MDS) is a rare genetic disorder, due to contiguous gene deletion on chromosome 17p13.3, characterized by classical type I lissencephaly, severe developmental delay, seizures, cardiac defects, and dysmorphisms.
Jewel Maria George, Carol Sara Cherian, Reji Thomas, Sebin Sunnychan   +3 more
doaj   +1 more source

Treatment of Infantile Spasms [PDF]

, 2011
Infantile spasms is an epileptic encephalopathy of early infancy with specific clinical and electroencephalographic (EEG) features, limited treatment options, and a poor prognosis.
Anna Catania, Tallie Z. Baram, Raili Riikonen, Tracy A. Glauser, Rogawski, Michael A, Pranzatelli, Michael R, Miguel A. Cortez, Baram, Tallie Z, Swann, John W, Catania, Anna, Michael R. Pranzatelli, Carl E. Stafstrom, Barry G. W. Arnason, Stafstrom, Carl E, Glauser, Tracy A, Shlomo Shinnar, Arnason, Barry GW, Michael A. Rogawski, Cortez, Miguel A, Riikonen, Raili, Shinnar, Shlomo, John W. Swann   +21 more
core   +1 more source

The spectrum of SCNIA-related infantile epileptic encephalopathies

, 2007
The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.
Zuberi, S., Connolly, M., Farrell, K., Andermann, F., Gardner, A., Sutherland, G., Dibbens, L., Andermann, E., Batish, S., Harbord, M., Iona, X., Harkin, L., Seltzer, W., Pelekanos, J., Wang, J., Gill, D., Stanley, T., Jones, J., McMahon, J., et al., Sadleir, L.   +20 more
core   +1 more source

The Clinical Features and Long-Term Follow-Up of Vitamin B6-Responsive Infantile Spasms in a Chinese Cohort

Frontiers in Neurology, 2022
ObjectiveTo analyze the clinical features, treatment, and prognosis of patients with vitamin B6-responsive infantile spasms (IS).MethodsThe clinical features, genetics, and follow-up data of 30 patients were collected and analyzed.ResultsThe age of ...
Xianru Jiao, Pan Gong, Yue Niu, Zhao Xu, Ye Wu, Yuehua Zhang, Zhixian Yang   +6 more
doaj   +1 more source

Infantile spasms syndrome, West syndrome and related phenotypes: what we know in 2013.

, 2014
The current spectrum of disorders associated to clinical spasms with onset in infancy is wider than previously thought; accordingly, its terminology has changed.
Pavone P, Falsaperla R, Ruggieri M., Pavone L, STRIANO, PASQUALE   +4 more
core   +2 more sources