Tracking Motor Progression and Device‐Aided Therapy Eligibility in Parkinson's Disease
ABSTRACT Objective To characterise the progression of motor symptoms and identify eligibility for device‐aided therapies in Parkinson's disease, using both the 5‐2‐1 criteria and a refined clinical definition, while examining differences across genetic subgroups.
David Ledingham +7 more
wiley +1 more source
Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome
ABSTRACT Objective Rett syndrome (RTT) is a devastating neurodevelopmental disorder with developmental regression affecting motor, sensory, and cognitive functions. Sensory disruptions contribute to the complex behavioral and cognitive difficulties and represent an important target for therapeutic interventions.
Alex Joseph Simon +12 more
wiley +1 more source
Two Mesolithic burials from Khor Shambat, Sudan [PDF]
The site of Khor Shambat 1 (KSH1) is located on the west bank of the Nile, in Omdurman, approximately 5 km north of Tuti Island. The first surveys there started in 2012, to be followed by an expedition of the Institute of Archaeology and Ethnology ...
Maciej Jórdeczka +1 more
doaj +1 more source
Effigy Vessel Documentation, Caddo Collections at the Texas Archeological Research Laboratory at The University of Texas at Austin [PDF]
Ceramic vessels from ancestral Caddo sites in East Texas are diverse in form, size, manufacture, and decoration, both spatially and temporally. Variation in these attributes, including vessel form as well as any attachments, also “is connected with ...
Perttula, Timothy K. +1 more
core +1 more source
Frailty Exacerbates Disability in Progressive Multiple Sclerosis
ABSTRACT Background To evaluate frailty in severe progressive multiple sclerosis (PMS) and to investigate the underlying mechanisms. Methods This prospective, cross‐sectional, multicenter study enrolled a late severe PMS group requiring skilled nursing (n = 53) and an age, sex, and disease duration‐matched control PMS group (n = 53).
Taylor R. Wicks +10 more
wiley +1 more source
Exploratory Analysis of ELP1 Expression in Whole Blood From Patients With Familial Dysautonomia
ABSTRACT Background Familial dysautonomia (FD) is a hereditary neurodevelopmental disorder caused by aberrant splicing of the ELP1 gene, leading to a tissue‐specific reduction in ELP1 protein expression. Preclinical models indicate that increasing ELP1 levels can mitigate disease manifestations.
Alejandra González‐Duarte +13 more
wiley +1 more source
ABSTRACT Objective Peripheral neuropathies contribute to patient disability but may be diagnosed late or missed altogether due to late referral, limitation of current diagnostic methods and lack of specialized testing facilities. To address this clinical gap, we developed NeuropathAI, an interpretable deep learning–based multiclass classification ...
Chaima Ben Rabah +7 more
wiley +1 more source
Chronological and Spatial Distribution of Skeletal Muscle Fat Replacement in FHL1‐Related Myopathies
ABSTRACT Objectives Variants in the FHL1 gene cause FHL1‐related myopathies (FHL1‐RMs), a group of neuromuscular disorders with diverse clinical presentations. This study aimed to comprehensively characterize the spatial and temporal patterns of skeletal muscle fat replacement throughout the whole body in FHL1‐RMs, to examine disease progression over ...
Rui Shimazaki +8 more
wiley +1 more source
Archaeological evidence for 9th and 8th millennia BC at Girmeler Cave near Tlos in SW Turkey
A mound settlement in front of the Girmeler Cave near the major Lycian city of Tlos in SW Turkey revealed evidence for occupation during the late 9th and 8th millennia BC.
Turan Takaoğlu +3 more
doaj +1 more source
The Monumental Cemeteries of Northern Pictland [PDF]
Peer reviewedPublisher ...
Mitchell, Juliette, Noble, Gordon
core +1 more source

