Results 91 to 100 of about 396,223 (265)
ABSTRACT Objective People with epilepsy (PWE) may experience cognitive deficits but fail to undergo formal evaluation. This study compares cognitive status between PWE and healthy controls in the West African Republic of Guinea. Methods A cross‐sectional, case–control study was conducted in sequential recruitment phases (July 2024–July 2025) at Ignace ...
Maya L. Mastick +14 more
wiley +1 more source
Simplified self-dual electrodynamics
We present a new formulation of self-dual nonlinear electrodynamics in which interactions are determined by an auxiliary-field potential, with causality ensuring a unique solution to the auxiliary-field equation.
Jorge G. Russo, Paul K. Townsend
doaj +1 more source
The Build-Up Construction for Codes over a Commutative Non-Unitary Ring of Order 9
The build-up method is a powerful class of propagation rules that generate self-dual codes over finite fields and unitary rings. Recently, it was extended to non-unitary rings of order 4, to generate quasi self-dual codes.
Adel Alahmadi +4 more
doaj +1 more source
Near-Extremal Type I Self-Dual Codes with Minimal Shadow over GF(2) and GF(4)
Binary self-dual codes and additive self-dual codes over GF(4) contain common points. Both have Type I codes and Type II codes, as well as shadow codes. In this paper, we provide a comprehensive description of extremal and near-extremal Type I codes over
Sunghyu Han
doaj +1 more source
Remote Monitoring in Myasthenia Gravis: Exploring Symptom Variability
ABSTRACT Background Myasthenia gravis (MG) is a rare, autoimmune disorder characterized by fluctuating muscle weakness and potential life‐threatening crises. While continuous specialized care is essential, access barriers often delay timely interventions. To address this, we developed MyaLink, a telemedical platform for MG patients.
Maike Stein +13 more
wiley +1 more source
Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy
ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan +3 more
wiley +1 more source
Remote Assessment of Ataxia Severity in SCA3 Across Multiple Centers and Time Points
ABSTRACT Objective Spinocerebellar ataxia type 3 (SCA3) is a genetically defined ataxia. The Scale for Assessment and Rating of Ataxia (SARA) is a clinician‐reported outcome that measures ataxia severity at a single time point. In its standard application, SARA fails to capture short‐term fluctuations, limiting its sensitivity in trials.
Marcus Grobe‐Einsler +20 more
wiley +1 more source
The build up construction for codes over a non-commutative non-unitary ring of order 9
The build-up method is a powerful class of propagation rules that generate self-dual codes over finite fields and unitary rings. Recently, it was extended to non-unitary rings of order four to generate quasi self-dual codes.
Adel Alahmadi +2 more
doaj +1 more source
Dual descriptions of massive spin-3 particles in $D=2+1$ via Noether gauge embedment
We present here a relationship among massive self-dual models for spin-3 particles in $D=2+1$ via the Noether Gauge Embedment $(NGE)$ procedure. Starting with a first order model (in derivatives) $S_{SD(1)}$ we have obtained a sequence of four self-dual ...
Dalmazi, D., Mendonça, E. L.
core +1 more source
Objective Australian evidence on lived and care experiences of chronic musculoskeletal shoulder pain (CMSP), irrespective of disorder classification or disease, is limited. However, such evidence is important for person‐centered care and informing local service pathways and care guidelines or standards.
Sonia Ranelli +8 more
wiley +1 more source

