Results 31 to 40 of about 202,677 (211)

Neuro-developmental and epilepsy outcomes of children with west syndrome: A cross-sectional study from North India

Annals of Indian Academy of Neurology, 2020
Objectives: To assess the neurodevelopmental outcome of West syndrome (WS) in Indian children, who differ in their clinical profile from the western population.
Juhi Gupta, Suvasini Sharma, Sharmila B Mukherjee, Puneet Jain, Satinder Aneja   +4 more
doaj   +1 more source

Valproate for Intractable Epilepsy

Pediatric Neurology Briefs, 1992
The efficacy and side effects of high dose valproic acid (VPA) therapy in 46 children with refractory epilepsy were studied at the Department of Child Neurology, Okayama University Medical School, Okayama, Japan.
J Gordon Millichap
doaj   +1 more source

Persistent hyperplastic primary vitreous in a child with incontinentia pigmenti and infantile spasms

Oman Journal of Ophthalmology, 2022
Incontinentia pigmenti (IP) is a rare neurocutaneous syndrome of X-linked dominant inheritance (1:40000 births in the Caucasian population) which is usually lethal in males.
Siddharth Madan, Zia Chaudhuri
doaj   +1 more source

Electroclinical Features of Infantile Epileptic Spasms Syndrome

Annals of Indian Academy of Neurology
Epileptic spasms are a unique, age-dependent manifestation of epilepsies in infancy and early childhood, commonly occurring as part of infantile epileptic spasms syndrome.
Gozde Erdemir, Ahsan N. Moosa
doaj   +1 more source

Surgery in West Syndrome

Pediatric Neurology Briefs, 1991
The results of surgical removal of a porencephalic cyst in an 18-month old child with infantile spasms and hypsarrhythmia are reported from the Departments of Neurology and Neurosurgery, VA Medical Center and University of Florida; the State University of Stony Brook, NY; and University of Michigan Medical School, Ann Arbor, MI.
openaire   +3 more sources

Wolf–Hirschhorn (4p-) syndrome with West syndrome

Epilepsy & Behavior Case Reports, 2016
Wolf-Hirschhorn syndrome (WHS) is a chromosome disorder (4p-syndrome) which is characterized by craniofacial features and epileptic seizures. Here, we report a case of WHS with West syndrome, in whom the seizures were refractory to several antiepileptic drugs but were responsive to the addition of lamotrigine.
Hirotaka Motoi, Hideo Enoki, Tomohiro Yamazoe, Mitsuyo Nishimura, Tohru Okanishi, Takuya Yokota, Takamichi Yamamoto, Ayataka Fujimoto, Sotaro Kanai   +8 more
openaire   +3 more sources

Quantification of Hypsarrhythmia in Infantile Spasmatic EEG: A Large Cohort Study

IEEE Transactions on Neural Systems and Rehabilitation Engineering
Infantile spasms (IS) is a neurological disorder causing mental and/or developmental retardation in many infants. Hypsarrhythmia is a typical symptom in the electroencephalography (EEG) signals with IS.
Ruolin Hou, Qiongru Guo, Qinman Wu, Zihao Zhao, Xindan Hu, Yumei Yan, Wenyuan He, Peize Lyu, Ruisheng Su, Tao Tan, Xiaoqiang Wang, Yuanning Li, Dake He, Lin Xu   +13 more
doaj   +1 more source

Developmental Trajectories of Hand Movements in Typical Infants and Those at Risk of Developmental Disorders: An Observational Study of Kinematics during the First Year of Life

Frontiers in Psychology, 2018
HighlightsThe kinematics of hand movements (spatial use, curvature, acceleration, and velocity) of infants with their mothers in an interactive setting are significantly associated with age in cohorts of typical and at-risk infantsdiffer significantly at
Lisa Ouss, Lisa Ouss, Marie-Thérèse Le Normand, Kevin Bailly, Marluce Leitgel Gille, Christelle Gosme, Roberta Simas, Julia Wenke, Xavier Jeudon, Stéphanie Thepot, Telma Da Silva, Xavier Clady, Edith Thoueille, Mohammad Afshar, Bernard Golse, Mariana Guergova-Kuras   +15 more
doaj   +1 more source

Hormonal Therapy for Infantile Spasms: A Systematic Review and Meta-Analysis

Frontiers in Neurology, 2022
ObjectiveThe limitations of adrenocorticotrophic hormone (ACTH) treatment for infantile spasms (ISs), such as high costs, limited availability, and adverse effects (AEs), make it necessary to explore whether corticosteroids are optimal alternatives. Many
Shiqi Guang, Leilei Mao, Linxiu Zhong, Fangyun Liu, Zou Pan, Fei Yin, Jing Peng   +6 more
doaj   +1 more source

Ictal SPECT Focal Hyperperfusion in West Syndrome

Pediatric Neurology Briefs, 2007
Ictal single photon emission computed tomography (SPECT) and EEG were used to determine the mechanism of clustered spasms in 3 patients with symptomatic West syndrome (WS), in a study at Tokushima University, Japan.
J Gordon Millichap
doaj   +1 more source