Results 101 to 110 of about 5,856,489 (275)
The rs10191329 Risk Allele Is Associated With Pronounced Retinal Layer Atrophy in Multiple Sclerosis
ABSTRACT Objective To investigate whether the rs10191329 risk allele in the DYSF–ZNF638 locus, which is implicated in central nervous system resilience rather than immune‐mediated pathology, is associated with retinal layer thinning, a biomarker of neuroaxonal damage in relapsing multiple sclerosis (RMS). Methods From a prospective observational study,
Gabriel Bsteh +22 more
wiley +1 more source
On modality in Georgian sign language (GESL) [PDF]
Modality is one of the most fascinating and complex areas of language studies. This paper illustrates the types of modal constructions in Georgian Sign language (GESL), including negative forms.
Makharoblidze, Tamar
core
ABSTRACT Objective Neurodegeneration with brain iron accumulation (NBIA) comprises rare genetic disorders characterized by predominantly extrapyramidal symptoms and iron deposition in the basal ganglia. Conventional magnetic resonance imaging (MRI) detects qualitative changes but cannot accurately quantify iron accumulation. Quantitative susceptibility
Özge Uygun +21 more
wiley +1 more source
A survey on mouth modeling and analysis for Sign Language recognition [PDF]
© 2015 IEEE.Around 70 million Deaf worldwide use Sign Languages (SLs) as their native languages. At the same time, they have limited reading/writing skills in the spoken language.
Antonakos, E, Roussos, A, Zafeiriou, S
core +2 more sources
Long‐Term Evaluation of Givinostat in Duchenne Muscular Dystrophy, and Natural History Comparisons
ABSTRACT Objectives This ongoing, open‐label extension study is evaluating the long‐term safety, tolerability, and efficacy of givinostat, a Class I and II histone deacetylase inhibitor, in patients with Duchenne muscular dystrophy (DMD). Methods The recruited patients completed one of two prior clinical studies (one Phase 2 and one Phase 3 [EPIDYS ...
Craig M. McDonald +74 more
wiley +1 more source
Barriers Faced by Deaf Individuals while Availing Speech and Hearing Services
Background and Aim: Deaf individuals in India face significant auditory impairment, leading to challenges in accessing services. Studies highlight the need to enhance communication services and accessibility to ensure fair access to resources for the ...
Reuben Thomas Varghese +5 more
doaj +1 more source
ABSTRACT Objective Autosomal dominant progranulin (GRN) pathogenic variants are a genetic cause of frontotemporal lobar degeneration. Though clinical trials for GRN‐related therapies are underway, there is an unmet need for biomarkers that can predict symptom onset and track disease progression.
Taru M. Flagan +46 more
wiley +1 more source
This research introduces a foundational framework aimed at bridging the communication gap between American Sign Language (ASL) and Indian Sign Language (ISL) by translating alphabet-level gestures. The proposed system employs a hybrid deep learning model
Malay Kumar +4 more
doaj +1 more source
Grammaticalisation processes in Flemish sign language [PDF]
Following Hopper & Traugott (2003 [1993]: 232), grammaticalisation can be defined as “the change whereby lexical items and constructions come in certain linguistic contexts to serve grammatical functions and, once grammaticalized, continue to develop new
Van Herreweghe, Mieke
core
ABSTRACT Objective Cognitive impairment (CI) affects the quality of life in multiple sclerosis (MS). Identifying influencing factors is key to improving CI monitoring. This systematic review and meta‐analysis examines clinical and sociodemographic variables impacting the cognitive screening Symbol Digit Modalities Test (SDMT) performance across MS ...
Katalin Lugosi +8 more
wiley +1 more source

