UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Novel Therapeutics for Neonatal Seizures

Neurotherapeutics, 2021-07, Vol.18 (3), p.1564-1581

2021

Volltextzugriff (PDF)

Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome

Annals of neurology, 2020-03, Vol.87 (3), p.339-346

2020

Volltextzugriff (PDF)

Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2

Epilepsia (Copenhagen), 2022-10, Vol.63 (10), p.e125-e131

2022

Volltextzugriff (PDF)

Thrombocytopenia in pediatric patients on concurrent cannabidiol and valproic acid

Epilepsia (Copenhagen), 2020-08, Vol.61 (8), p.e85-e89

2020

Volltextzugriff (PDF)

An Implantable Micro-Caged Device for Direct Local Delivery of Agents

Scientific reports, 2017-12, Vol.7 (1), p.17624-16, Article 17624

2017

Volltextzugriff (PDF)

Measure thrice, cut twice: On the benefit of reoperation for failed pediatric epilepsy surgery

Epilepsy research, 2020-03, Vol.161, p.106289-106289, Article 106289

2020

Volltextzugriff (PDF)

Frequency of and factors associated with antiseizure medication discontinuation discussions and decisions in patients with epilepsy: A multicenter retrospective chart review

Epilepsia open, 2023-06, Vol.8 (2), p.371-385

2023

Volltextzugriff (PDF)

Variation in seizure risk increases from antiseizure medication withdrawal among patients with well-controlled epilepsy: A pooled analysis

Epilepsia open, 2024-02, Vol.9 (1), p.333-344

2024

Volltextzugriff (PDF)

P567: Innovations in education: Empowering child neurology residents with basic concepts in genomic testing through a national curriculum

Genetics in Medicine Open, 2024, Vol.2, p.101466, Article 101466

2024

Volltextzugriff (PDF)

Endocannabinoids block status epilepticus in cultured hippocampal neurons

European journal of pharmacology, 2007-03, Vol.558 (1), p.52-59

2007

Volltextzugriff (PDF)

An organotypic hippocampal slice culture model of excitotoxic injury induced spontaneous recurrent epileptiform discharges

Brain research, 2011-01, Vol.1371, p.110-120

2011

Volltextzugriff (PDF)

Carisbamate prevents the development and expression of spontaneous recurrent epileptiform discharges and is neuroprotective in cultured hippocampal neurons

Epilepsia (Copenhagen), 2008-10, Vol.49 (10), p.1795-1802

2008

Volltextzugriff (PDF)

Long‐Term Downregulation of the Sodium Channel Gene Scn8a Is Therapeutic in Mouse Models of SCN8A Epilepsy

Annals of neurology, 2024-04, Vol.95 (4), p.754-759

2024

Volltextzugriff (PDF)

Allele-Specific Editing of a Dominant SCN8A Epilepsy Variant Protects against Seizures and Lethality in a Murine Model

Annals of neurology, 2024-08

2024

Volltextzugriff (PDF)

Neonatal Seizures: Diagnosis, Etiologies, and Management

Seminars in neurology, 2020-04, Vol.40 (2), p.246-256

2020

Volltextzugriff (PDF)

Abstract 12541: Development of a Transgenic Rabbit Model of Dravet Syndrome

Circulation (New York, N.Y.), 2022-11, Vol.146 (Suppl_1)

2022

Volltextzugriff (PDF)

A gain‐of‐function GRIA2 variant associated with neurodevelopmental delay and seizures: Functional characterization and targeted treatment

Epilepsia (Copenhagen), 2022-12, Vol.63 (12), p.e156-e163

2022

Volltextzugriff (PDF)

Current Treatment Strategies and Future Treatment Options for Dravet Syndrome

Current treatment options in neurology, 2018-12, Vol.20 (12), p.52-52, Article 52

2018

Volltextzugriff (PDF)

Sudden Unexpected Death in Epilepsy and Respiratory Defects in a Mouse Model of DEPDC5‐Related Epilepsy

Annals of neurology, 2023-11, Vol.94 (5), p.812-824

2023

Volltextzugriff (PDF)

Defining the latent period of epileptogenesis and epileptogenic zone in a focal cortical dysplasia type II (FCDII) rat model

Epilepsia (Copenhagen), 2021-05, Vol.62 (5), p.1268-1279

2021

Volltextzugriff (PDF)

Loss of CLOCK Results in Dysfunction of Brain Circuits Underlying Focal Epilepsy

Neuron (Cambridge, Mass.), 2017-10, Vol.96 (2), p.387-401.e6

2017

Volltextzugriff (PDF)

Neonatal Seizures: New Evidence, Classification, and Guidelines

Epilepsy currents, 2024-05

2024

Volltextzugriff (PDF)

Clinical Reasoning: A 15-month-old boy with progressive lethargy and spasticity

Neurology, 2017-09, Vol.89 (12)

2017

Volltextzugriff (PDF)

Epilepsy and sudden unexpected death in epilepsy in a mouse model of human SCN1B-linked developmental and epileptic encephalopathy

Brain communications, 2023, Vol.5 (6), p.fcad283-fcad283

2023

Volltextzugriff (PDF)

1 – 25 von 27

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(26)
Mit Volltextzugriff
(24)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Epilepsia
(5)
Annals Of Neurology
(4)
Epilepsia Open
(2)
Brain Communications
(1)
Brain Research
(1)
Circulation
(1)
Current Treatment Options In Neurology
(1)
Epilepsy Currents
(1)
Epilepsy Research
(1)
Epiliepsy Currents/epilepsy Currents
(1)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Novel Therapeutics for Neonatal Seizures

Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome

Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2

Thrombocytopenia in pediatric patients on concurrent cannabidiol and valproic acid

An Implantable Micro-Caged Device for Direct Local Delivery of Agents

Measure thrice, cut twice: On the benefit of reoperation for failed pediatric epilepsy surgery

Frequency of and factors associated with antiseizure medication discontinuation discussions and decisions in patients with epilepsy: A multicenter retrospective chart review

Variation in seizure risk increases from antiseizure medication withdrawal among patients with well-controlled epilepsy: A pooled analysis

P567: Innovations in education: Empowering child neurology residents with basic concepts in genomic testing through a national curriculum

Endocannabinoids block status epilepticus in cultured hippocampal neurons

An organotypic hippocampal slice culture model of excitotoxic injury induced spontaneous recurrent epileptiform discharges

Carisbamate prevents the development and expression of spontaneous recurrent epileptiform discharges and is neuroprotective in cultured hippocampal neurons

Long‐Term Downregulation of the Sodium Channel Gene Scn8a Is Therapeutic in Mouse Models of SCN8A Epilepsy

Allele-Specific Editing of a Dominant SCN8A Epilepsy Variant Protects against Seizures and Lethality in a Murine Model

Neonatal Seizures: Diagnosis, Etiologies, and Management

Abstract 12541: Development of a Transgenic Rabbit Model of Dravet Syndrome

A gain‐of‐function GRIA2 variant associated with neurodevelopmental delay and seizures: Functional characterization and targeted treatment

Current Treatment Strategies and Future Treatment Options for Dravet Syndrome

Sudden Unexpected Death in Epilepsy and Respiratory Defects in a Mouse Model of DEPDC5‐Related Epilepsy

Defining the latent period of epileptogenesis and epileptogenic zone in a focal cortical dysplasia type II (FCDII) rat model

Loss of CLOCK Results in Dysfunction of Brain Circuits Underlying Focal Epilepsy

Neonatal Seizures: New Evidence, Classification, and Guidelines

Clinical Reasoning: A 15-month-old boy with progressive lethargy and spasticity

Gene-Targeted Therapies in Pediatric Neurology: Challenges and Opportunities in Diagnosis and Delivery

Epilepsy and sudden unexpected death in epilepsy in a mouse model of human SCN1B-linked developmental and epileptic encephalopathy

Suchergebnisse filtern