ABSTRACT Objective To explore how cerebral hypoxia and Normal‐Appearing White Matter (NAWM) integrity affect MS lesion burden and clinical course. Methods Seventy‐nine MS patients, including 13 clinically isolated syndrome (CIS) patients and 66 relapsing–remitting multiple sclerosis (RRMS) patients, and 44 healthy controls (HCs) were recruited from ...
Xinli Wang +8 more
wiley +1 more source
Hospital-Acquired Pneumonia: Etiology and Antimicrobial Therapy
Hospital-acquired pneumonia (HAP) is a common and severe complication of critically ill patients. It has been associated with increased length of stay in the hospital and intensive care unit, as well as to high mortality rates.
Medeiros, Eduardo Alexandrino Servolo [UNIFESP]
core
Delayed diagnosis of ocular myasthenia gravis in a patient with aponeurotic ptosis: A case report. [PDF]
Xie J, Zhang H, Ye J.
europepmc +1 more source
ABSTRACT Objective Onasemnogene abeparvovec (OA) is an AAV9‐based gene therapy for spinal muscular atrophy type I (SMA I). Real‐world outcomes show increased response variability compared to clinical trials, and follow‐up data beyond 12–18 months are limited.
Marika Pane +43 more
wiley +1 more source
The incidence and outcomes of hospital acquired- bloodstream infection and ventilator associated pneumonia and the impact of infectious diseases referral using data from the clinically-oriented antimicrobial resistance surveillance network for healthcare-associated infections (ACORN-HAI): An interim report. [PDF]
Co-Chang SN, Terre NBS, Abad CLR.
europepmc +1 more source
Clinical Validation of Plasma p‐217tau in Neurological Diseases
ABSTRACT Objective Plasma p‐217tau is a minimally invasive but specific biomarker for diagnosing Alzheimer's disease (AD). However, its disease specificity remains to be clinically evaluated. We validated the reliability of the p‐217tau biomarker in 12 other neurological diseases.
Takeshi Kawarabayashi +13 more
wiley +1 more source
Diagnostic discordance and differential diagnoses of community-acquired pneumonia in the emergency department. [PDF]
Simon S +6 more
europepmc +1 more source
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
Case Report: A hidden cause of severe hemorrhage: a diagnostic and therapeutic challenge. [PDF]
Han Z, Ruan J, Wang L, Wang W, Zhu T.
europepmc +1 more source
Hospital-acquired staphylococcal disease and the community.
F H, WENTWORTH +2 more
openaire +1 more source

