Results 151 to 160 of about 3,363,963 (290)

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru   +13 more
wiley   +1 more source

Recovery trajectories and predictors of symptom resolution in post-COVID-19 condition: a population-based cohort study. [PDF]

open access: yesLancet Reg Health Eur
Brunet JL   +4 more
europepmc   +1 more source

Condition Monitoring and Prognosis for Subsea Multiphase Pump

open access: yes, 2015
This thesis presents a case study about the condition monitoring of the twin-screw multiphase pump in the subsea field to demonstrate how condition monitoring techniques can be applied for subsea equipment. Firstly a FMECA (Failure modes, effects, and criticality analysis) worksheet is carried out to identify the critical components of a twin-screw ...
openaire   +1 more source

Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Despite its monogenic origin, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy exhibits marked variability in clinical expression and severity. Variants in the NOTCH3 gene, within epidermal growth factor‐like repeat domains 1–6 or 7–34, are known to influence disease onset, but their impact ...
Léa Aguilhon   +5 more
wiley   +1 more source

Correlation Between Serum Inflammatory Factor Level Changes and Disease Severity in Patients with Chronic Obstructive Pulmonary Disease Complicated by Tuberculosis

open access: yesInternational Journal of General Medicine
Yiyao Di,1,* Fan Yang,2,* Conglu Che,3 Shenghui Xu,4 Ying Qi3 1Respiratory Department, Affiliated Hospital of Hebei University, Baoding, Hebei, People’s Republic of China; 2Emergency Department II, Baoding First Central Hospital, Baoding,
Di Y, Yang F, Che C, Xu S, Qi Y
doaj  

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li   +11 more
wiley   +1 more source

Sex‐Stratified Association of Regional Dopamine Transporter Binding With Disease Progression in Amyotrophic Lateral Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To clarify the clinical relevance of dopamine transporter single‐photon emission computed tomography (DAT‐SPECT) abnormalities in amyotrophic lateral sclerosis (ALS), with a prespecified focus on sex‐stratified associations with disease progression and short‐term prognosis.
Tomoya Kawazoe   +7 more
wiley   +1 more source

Home - About - Disclaimer - Privacy