Results 171 to 180 of about 2,272,583 (371)

Immediate Therapeutic Response to Vigabatrin in Lissencephaly‐Related Epileptic Spasms due to TUBA1A R402H Variant

open access: yes
American Journal of Medical Genetics Part A, EarlyView.
Toru Nagata   +6 more
wiley   +1 more source

Identifying the optimal dose of cannabidiol by intrabuccal administration in Kramnik (C3HeB/FeJ) mice

open access: yesAnimal Models and Experimental Medicine, EarlyView.
Cannabidiol (CBD) has numerous therapeutic properties, and is used to treat neurological conditions, such as neuroinflammation. However, the optimal dose of CBD to penetrate the brain requires further investigation. The primary aim of this study was to use a mouse model and the intrabuccal route for CBD administration to determine the optimal dose at ...
Oluwadara Pelumi Omotayo   +4 more
wiley   +1 more source

A Longer Polyalanine Expansion Mutation in the ARX Gene Causes Early Infantile Epileptic Encephalopathy with Suppression-Burst Pattern (Ohtahara Syndrome) [PDF]

open access: bronze, 2007
Mitsuhiro Kato   +8 more
openalex   +1 more source

Automated Detection of Isolated REM Sleep Behavior Disorder Using Computer Vision

open access: yesAnnals of Neurology, EarlyView.
Objective Isolated rapid eye movement (REM) sleep behavior disorder (iRBD) is, in most cases, an early stage of Parkinson's disease or related disorders. Diagnosis requires an overnight video‐polysomnogram (vPSG), however, even for sleep experts, interpreting vPSG data is challenging.
Mohamed Abdelfattah   +11 more
wiley   +1 more source

Modeling Sporadic Progressive Supranuclear Palsy in 3D Midbrain Organoids: Recapitulating Disease Features for In Vitro Diagnosis and Drug Discovery

open access: yesAnnals of Neurology, EarlyView.
Objective Progressive Supranuclear Palsy (PSP) is a severe neurodegenerative disease characterized by tangles of hyperphosphorylated tau protein and tufted astrocytes. Developing treatments for PSP is challenging due to the lack of disease models reproducing its key pathological features.
Elvira Immacolata Parrotta   +15 more
wiley   +1 more source

Neuroleptic Malignant Syndrome‐like State in an Epileptic Patient with Organic Brain Comorbidity Treated with Zonisamide and Carbamazepine [PDF]

open access: bronze, 2007
Hideki Azuma   +5 more
openalex   +1 more source

Clinical Relevance of ‘Cap’ and ‘Track’ Development after Recent Small Subcortical Infarct

open access: yesAnnals of Neurology, EarlyView.
Objective After a recent small subcortical infarct (RSSI), some patients develop perilesional or remote hyperintensities (‘caps/tracks’) to the index infarct on T2/FLAIR MRI. However, their clinical relevance remains unclear. We investigated the clinicoradiological correlates of ‘caps/tracks’, and their impact on long‐term outcomes following RSSI ...
Yajun Cheng   +24 more
wiley   +1 more source

Epilepsy, EEG and chromosomal rearrangements

open access: yesEpilepsia Open
Chromosomal abnormalities are associated with a broad spectrum of clinical manifestations, one of the more commonly observed of which is epilepsy.
Justyna Paprocka   +4 more
doaj   +1 more source

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