Results 151 to 160 of about 64,748,975 (303)
ABSTRACT Objective The aim of this study was to characterize intellectual and motor function, neurological features including epilepsy, treatment response, and adaptive behavior in patients with pyruvate dehydrogenase complex deficiency (PDCD) in Sweden.
Antri Savvidou +6 more
wiley +1 more source
Navigating the adaptation of CBT for persons with disabilities in South Africa: An autoethnographic perspective. [PDF]
Kunutu R, Ntshangase S.
europepmc +1 more source
Fatality Review Board for Persons with Disabilities report
Biennial; Began with 2004/2005.; Description based on first and only issue; title from cover.; Report year ends June 30.; Harvested from the web on 7/6 ...
Connecticut. Fatality Review Board for Persons with Disabilities.
core
Inebilizumab in AQP4‐Seropositive NMOSD: One‐Year Follow‐Up From a Multicenter, Real‐World Study
ABSTRACT Objective Real‐world evidence on inebilizumab among neuromyelitis optica spectrum disorder (NMOSD) patients is lacking. This study assessed inebilizumab among Chinese patients with aquaporin 4 autoantibody (AQP4‐IgG)‐seropositive NMOSD in a real‐world setting.
Mengcui Gui +10 more
wiley +1 more source
On the occasion of the 10th 'scaling with love' event to promote oral health for persons with disabilities. [PDF]
Min KM.
europepmc +1 more source
Other title: Fatality Review Board for Persons with Disabilities report
Biennial; Began with 2004/2005.; Description based on first and only issue; title from cover.; Report year ends June 30.; Harvested from the web on 1/12 ...
Connecticut. Fatality Review Board for Persons with Disabilities.
core
ABSTRACT Objective Neuromyelitis optica spectrum disorder (NMOSD) is a devastating neurological disease that lacks serological biomarkers that can accurately reflect disease activity. We established a live cell‐based assay (LCBA) using serum with endogenous complement to quantify the overall cytotoxicity, offering a novel functional tool for monitoring
Xiaona Xu +10 more
wiley +1 more source
ABSTRACT Objective CDKL5 deficiency disorder (CDD) is a rare, severe developmental and epileptic encephalopathy. There is a pressing need to develop effective and sustainable therapeutic strategies. We aimed to investigate the causal association between febrile episodes and epileptic seizures for therapeutic implications in CDD patients.
Siyi Wang +13 more
wiley +1 more source
Enhancing healthcare access for persons with disabilities: lessons from partnerships between organisations of persons with disabilities and international non-governmental organisations. [PDF]
Hall P, Walsh C, Elliott C, Trimmel J.
europepmc +1 more source
Data‐Driven SuStaIn Model of Disability Progression in Amyotrophic Lateral Sclerosis
ABSTRACT Objective To determine whether ordinal Subtype and Stage Inference (SuStaIn) applied to routine ALSFRS‐R item scores can identify reproducible disability progression patterns in amyotrophic lateral sclerosis (ALS) and provide clinically meaningful staging.
Giammarco Milella +5 more
wiley +1 more source

