Results 51 to 60 of about 2,372,972 (378)

Treatment Duration for Absence Epilepsy

Pediatric Neurology Briefs, 1995
The effects of 6 months of treatment followed by a 5- to 6-week withdrawal period of ethosuximide (ESM) in 3 children, ages 5, 10, and 10 years, with new onset absence epilepsy are reported from the Departments of Neurology, State University of New York ...
J Gordon Millichap
doaj   +1 more source

Autism and mild epilepsy associated with a de novo missense pathogenic variant in the GTPase effector domain of DNM1

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView., 2023
Abstract Dynamin 1 is a GTPase protein involved in synaptic vesicle fission, which facilitates the exocytosis of neurotransmitters necessary for normal signaling. Pathogenic variants in the DNM1 gene are associated with intractable epilepsy, often manifested as infantile spasms at onset, developmental delay, and a movement disorder, and are located in ...
Davide Mei, Elena Parrini, Claudia Bianchini, Maria Luisa Ricci, Renzo Guerrini   +4 more
wiley   +1 more source

Absence Epilepsy and Moyamoya Disease

Pediatric Neurology Briefs, 2006
The case of a 6-year-old girl with typical absence epilepsy associated with moyamoya disease (MMD) is reported from the Department of Neurosurgery, Kyoto University Graduate School of Medicine, Japan.
J Gordon Millichap
doaj   +1 more source

A case of recurrent epilepsy-associated rosette-forming glioneuronal tumor with anaplastic transformation in the absence of therapy. [PDF]

, 2019
Rosette-forming glioneuronal tumor (RGNT) most commonly occurs adjacent to the fourth ventricle and therefore rarely presents with epilepsy. Recent reports describe RGNT occurrence in other anatomical locations with considerable morphologic and genetic ...
Corless, Christopher L, Ferris, Sean P, Grafe, Marjorie, Gultekin, Sakir H, Halfpenny, Aaron, Lawce, Helen, Lucas, Lora, Moore, Stephen, Nazemi, Kellie, Olson, Susan, Perry, Arie, Selden, Nathan, Solomon, David A, Woltjer, Randy, Wood, Matthew D   +14 more
core   +1 more source

Thyroid function and epilepsy: a two-sample Mendelian randomization study

Frontiers in Human Neuroscience
BackgroundThyroid hormones (THs) play a crucial role in regulating various biological processes, particularly the normal development and functioning of the central nervous system (CNS).
Di Lu, Di Lu, Yunming Wang, Yunming Wang, Yanfeng Yang, Yanfeng Yang, Huaqiang Zhang, Huaqiang Zhang, Xiaotong Fan, Xiaotong Fan, Sichang Chen, Sichang Chen, Penghu Wei, Penghu Wei, Penghu Wei, Yongzhi Shan, Yongzhi Shan, Guoguang Zhao, Guoguang Zhao, Guoguang Zhao   +19 more
doaj   +1 more source

Effects of Probiotic Consumption on Absence Seizures

Archives of Epilepsy, 2017
Objectives:Probiotics are microorganisms of intestinal microflora that are beneficial for human health. Childhood absence epilepsy has 2 validated rat models: Genetic Absence Epilepsy Rats from Strasbourg (GAERS) and Wistar Albino Glaxo from Rijswijk ...
Serdar AKKOL, Mehmet Can DOĞAN, Duygu ESENKAR, Handan DOĞAN, Tuğba KARAMAHMUTOĞLU, Filiz ONAT   +5 more
doaj   +1 more source

Astrocytes and absence epilepsy [PDF]

British Journal of Pharmacology, 2013
This article is a commentary on the research paper by Yamamura et al., pp. 1088‐1100 of this issue.
openaire   +2 more sources

Carbamazepine Exacerbation of Absence Epilepsy

Pediatric Neurology Briefs, 1998
The inappropriate use of carbamazepine (CBZ) in 8 children, and vigabatrin (VGB) in 2, among 18 consecutive referrals of children with resistant typical absence seizures, is reported from St Thomas’ and Guy’s Hospitals, London, UK.
J Gordon Millichap
doaj   +1 more source

Establishing an assay to evaluate d‐amino acid oxidase enzyme kinetics and inhibition using WST‐8 redox dye

FEBS Open Bio, EarlyView.
This study investigated a novel WST‐8‐based assay for evaluating d‐Amino acid oxidase (DAO) inhibitors. We confirmed its effectiveness using known inhibitors and found that uremic toxins possess relatively weak inhibitory activity compared to existing drugs.
Kahoko Miyake, Yuki Enoki, Yuka Nakazawa, Kazuaki Taguchi, Kazuaki Matsumoto   +4 more
wiley   +1 more source

Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz, Josefine Eck, Joel S. Winston, Kate Baker   +3 more
wiley   +1 more source