Results 161 to 170 of about 176,942 (307)

Functional signatures of de novo GABBR1 and GABBR2 variants associated with neurodevelopmental disorders. [PDF]

NPJ Genom Med
Stawarski M, Bielopolski N, Roitman I, Fridman K, Wald-Altman S, Eitel M, Hui B, Vulto-van Silfhout A, Stegmann APA, Chirita-Emandi A, Eason J, Bradshaw K, Darnell L, Kostrzewa G, Ploski R, Meurs R, Batté A, Antonarakis SE, Gassmann M, Bettler B.   +19 more
europepmc   +1 more source

New insights into epileptic spasm generation and treatment from the TTX animal model

Epilepsia Open, EarlyView.
Abstract Currently, we have an incomplete understanding of the mechanisms underlying infantile epileptic spasms syndrome (IESS). However, over the past decade, significant efforts have been made to develop IESS animal models to provide much‐needed mechanistic information for therapy development.
John W. Swann, Carlos J. Ballester‐Rosado, Chih‐Hong Lee   +2 more
wiley   +1 more source

Gut-Brain Signaling in Parkinson's Disease: A Narrative Review. [PDF]

Int J Mol Sci
Ratajczyk K, Kaczorowska E, Wyka K, Tarasiuk-Zawadzka A, Fichna J, Gajos A.   +5 more
europepmc   +1 more source

Precision therapies for genetic epilepsies in 2025: Promises and pitfalls

Epilepsia Open, EarlyView.
Abstract By targeting the underlying etiology, precision therapies offer an exciting paradigm shift to improve the stagnant outcomes of drug‐resistant epilepsies, including developmental and epileptic encephalopathies. Unlike conventional antiseizure medications (ASMs) which only treat the symptoms (seizures) but have no effect on the underlying ...
Shuyu Wang, Emilio Perucca, Samuel F. Berkovic, Piero Perucca   +3 more
wiley   +1 more source

Editorial: The interplay between GABA and glutamate in systems physiology and pathophysiology. [PDF]

Front Pharmacol
Rivera C, Lewis SJ.
europepmc   +1 more source

Absence seizures: Update on signaling mechanisms and networks

Epilepsia Open, EarlyView.
Abstract Absence seizures (AS) are a hallmark of genetic generalized epilepsies (GGE), characterized by brief episodes of impaired consciousness accompanied by electroencephalographic spike‐and‐wave discharges (SWDs). Traditionally attributed to cortico‐thalamo‐cortical (CTC) dysrhythmia, emerging evidence suggests a more intricate pathophysiological ...
Ozlem Akman, Filiz Onat
wiley   +1 more source

Neurotransmitter signaling in white matter [PDF]

, 2014
Butt, Arthur M., Fern, Robert F., Matute, Carlos   +2 more
core   +1 more source

Excitatory GABA receptors shape locomotor circuit organization in C. elegans. [PDF]

Sci Rep
Wang X, Mizuguchi K, Hashimoto K.
europepmc   +1 more source

Prenatal betamethasone–postnatal N‐methyl‐D‐aspartic acid model of spasms: Update on mechanisms and treatments

Epilepsia Open, EarlyView.
Abstract Infantile epilepsy spasms syndrome (IESS), formerly known as infantile spasms or West Syndrome, is a severe epilepsy syndrome affecting about 3 in 10,000 newborns in the United States. Characterized by clusters of epileptic spasms, interictal hypsarrhythmia, and developmental delays, IESS has diverse causes, including structural‐metabolic ...
Kayla Vieira, Antonia Schonwald, Chian‐Ru Chern, Kamya Shah, Jana Velíšková, Libor Velíšek   +5 more
wiley   +1 more source

Vagal GABAergic signaling in autonomic control of cardiometabolic function. [PDF]

Am J Physiol Cell Physiol
Boychuk CR, Wang YB.
europepmc   +1 more source