Results 151 to 160 of about 11,679 (284)
Advances in Somatic Embryogenesis of Banana. [PDF]
Adero M, Tripathi JN, Tripathi L.
europepmc +1 more source
This is a transcript of the daily journal of the expedition, as written by John Forbes in 1758. Friday, 7th of July, receiv\u27d the Governor\u27s Commission appointing me Chaplain to the 3d Battalion of the Pennsylvania Regiment, commanded by Colonel ...
core
Abstract Objective This work was undertaken to study the association between vagus nerve stimulation (VNS) parameters and the apnea–hypopnea index (AHI) measured by polysomnography in patients with drug‐resistant epilepsy. Methods Patients with epilepsy who underwent polysomnography with an active VNS device between 2018 and 2023 were retrospectively ...
Jacques‐François Massa +8 more
wiley +1 more source
Alteration in skin mycobiome due to atopic dermatitis and seborrheic dermatitis. [PDF]
Jung WH.
europepmc +1 more source
Rhythms in longitudinal thalamic recordings are linked to seizure risk
Abstract Objective Seizure unpredictability remains a major clinical challenge for people with epilepsy. Previous works have shown that seizure risk is associated with circadian and multi‐day cycles in both brain and physiological signals. However, it remains unclear whether neural activity from deep brain structures such as the anterior nucleus of the
Xinbing Zhang +5 more
wiley +1 more source
Scalp Melanoma in a Young Patient With Systemic Sarcoidosis: Multidisciplinary Approach. [PDF]
Mori N +17 more
europepmc +1 more source
Matching different-structured advertising pictorial metaphors with verbalization forms: incongruity-based evoked response potentials evidence. [PDF]
Cao S +5 more
europepmc +1 more source
Occipital spikes of the blind: Insights from EEG source localization
Epileptic Disorders, EarlyView.
Agilda Dema, Douglas Nordli III
wiley +1 more source
Long‐lasting remodeling of astrocytes in an Scna1+/− mouse model of Dravet syndrome
Abstract Objective Dravet syndrome (DS) is a prototypical developmental and epileptic encephalopathy caused by mutations in the SCN1A gene, leading to loss of function of the voltage‐gated sodium channel Naᵥ1.1. The latter causes early onset drug‐resistant seizures and enduring cognitive and behavioral deficits.
Athénaïs Genin +10 more
wiley +1 more source

