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Drug resistance in epilepsy: clinical impact, potential mechanisms, and new innovative treatment options
W Löscher, H Potschka, SM Sisodiya… - Pharmacological reviews, 2020 - Elsevier
Epilepsy is a chronic neurologic disorder that affects over 70 million people worldwide.
Despite the availability of over 20 antiseizure drugs (ASDs) for symptomatic treatment of …
Despite the availability of over 20 antiseizure drugs (ASDs) for symptomatic treatment of …
Neuronal hyperexcitability in Alzheimer's disease: what are the drivers behind this aberrant phenotype?
Alzheimer's disease (AD) is a progressive neurodegenerative disorder leading to loss of
cognitive abilities and ultimately, death. With no cure available, limited treatments mostly …
cognitive abilities and ultimately, death. With no cure available, limited treatments mostly …
Developmental and epileptic encephalopathies: what we do and do not know
N Specchio, P Curatolo - Brain, 2021 - academic.oup.com
Developmental encephalopathies, including intellectual disability and autistic spectrum
disorder, are frequently associated with infant epilepsy. Epileptic encephalopathy is used to …
disorder, are frequently associated with infant epilepsy. Epileptic encephalopathy is used to …
Animal toxins—Nature's evolutionary-refined toolkit for basic research and drug discovery
Venomous animals have evolved toxins that interfere with specific components of their
victim's core physiological systems, thereby causing biological dysfunction that aids in prey …
victim's core physiological systems, thereby causing biological dysfunction that aids in prey …
[HTML][HTML] Structural basis of Nav1. 7 inhibition by a gating-modifier spider toxin
Voltage-gated sodium (Nav) channels are targets of disease mutations, toxins, and
therapeutic drugs. Despite recent advances, the structural basis of voltage sensing …
therapeutic drugs. Despite recent advances, the structural basis of voltage sensing …
Sodium channelopathies in neurodevelopmental disorders
The voltage-gated sodium channel α-subunit genes comprise a highly conserved gene
family. Mutations of three of these genes, SCN1A, SCN2A and SCN8A, are responsible for a …
family. Mutations of three of these genes, SCN1A, SCN2A and SCN8A, are responsible for a …
Sodium channelopathies of skeletal muscle and brain
M Mantegazza, S Cestèle… - Physiological …, 2021 - journals.physiology.org
Voltage-gated sodium channels initiate action potentials in nerve, skeletal muscle, and other
electrically excitable cells. Mutations in them cause a wide range of diseases. These …
electrically excitable cells. Mutations in them cause a wide range of diseases. These …
Epilepsy-related voltage-gated sodium channelopathies: a review
LFS Menezes, EF Sabiá Júnior, DV Tibery… - Frontiers in …, 2020 - frontiersin.org
Epilepsy is a disease characterized by abnormal brain activity and a predisposition to
generate epileptic seizures, leading to neurobiological, cognitive, psychological, social, and …
generate epileptic seizures, leading to neurobiological, cognitive, psychological, social, and …
Antibodies and venom peptides: new modalities for ion channels
Ion channels play fundamental roles in both excitable and non-excitable tissues and
therefore constitute attractive drug targets for myriad neurological, cardiovascular and …
therefore constitute attractive drug targets for myriad neurological, cardiovascular and …
Guidance on Dravet syndrome from infant to adult care: road map for treatment planning in Europe
E Cardenal‐Muñoz, S Auvin, V Villanueva… - Epilepsia …, 2022 - Wiley Online Library
Dravet syndrome (DS) is a severe, rare, and complex developmental and epileptic
encephalopathy affecting 1 in 16 000 live births and characterized by a drug‐resistant …
encephalopathy affecting 1 in 16 000 live births and characterized by a drug‐resistant …