Results 151 to 160 of about 1,990,907 (242)

Characterization of Clinical Phenotype to Glial Fibrillary Acidic Protein Concentrations in Alexander Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To determine the concentration of glial fibrillary acidic protein (GFAP) in cerebrospinal fluid (CSF) and plasma in Alexander disease (AxD) and whether GFAP levels are predictive of disease phenotypes. Methods CSF and plasma were collected (longitudinally when available) from AxD participants and non‐AxD controls.
Amy T. Waldman, Asako Takanohashi, Joshua Y. Joung, Geraldine W. Liu, Kaley Arnold, Amy Pizzino, Walter Faig, Sarah Woidill, Sona Narula, Adeline L. Vanderver   +9 more
wiley   +1 more source

Nurses' Decisions to Press Charges Against Hypothetical Patients Who Exhibit Violent Behavior. [PDF]

Nurs Rep
Copeland D, Tipton S, Culter D, Potter M.   +3 more
europepmc   +1 more source

Unraveling the Molecular Mechanisms of Glioma Recurrence: A Study Integrating Single‐Cell and Spatial Transcriptomics

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Glioma recurrence severely impacts patient prognosis, with current treatments showing limited efficacy. Traditional methods struggle to analyze recurrence mechanisms due to challenges in assessing tumor heterogeneity, spatial dynamics, and gene networks.
Lei Qiu, Yinjiao Fei, Jiaxuan Ding, Kexin Shi, Jinyan Luo, Yuchen Zhu, Xingjian Sun, Gefei Jiang, Yuandong Cao, Weilin Xu, Shu Zhou   +10 more
wiley   +1 more source

Advanced oxidation processes at water/hydrophobic interfaces: energy-fluctuation mechanism and electron utilization quantification. [PDF]

Chem Sci
Xu G, Li F, Ye J, Zhang S, Ma H, Zhou G, Xu C, He X, Yang X, Song Q.   +9 more
europepmc   +1 more source

Spinal Cord Infarction Versus Idiopathic Transverse Myelitis: Clinical, Radiological, and Functional Insights From a Retrospective Cohort Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Spinal cord infarction (SCI) is a rare but devastating myelopathy, characterized by a high disability rate and an unfavorable prognosis. It has often been underdiagnosed and misdiagnosed as idiopathic transverse myelitis (ITM). This study aimed to describe the clinical features, radiological biomarkers, treatments, and functional ...
Zeqiang Ji, Jianlong Zhang, Yiming Shi, Shiyu Shan, Yang Du, Guangshuo Li, Ying Jin, Yani Zhang, Chuanying Wang, Yijun Lin, Yuhao Guo, Decai Tian, Xingquan Zhao, Tian Song   +13 more
wiley   +1 more source

Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan, Elizabeth I. Pierpont, Amena S. Fine, Reena V. Kartha   +3 more
wiley   +1 more source

James H. Simpson 2003 Navaho Expedition. Journal of a Military Reconnaissance from Santa Fe, New Mexico, to the Navaho Country, Made in 1849. Norman: University of Oklahoma Press.

Bulletin of the History of Archaeology, 2004
Jonathan E. Reyman
doaj   +1 more source

A Summative Usability Evaluation of an Infusion Pump Through Simulation-Based Testing With Nurses: Mixed Approach Study.

JMIR Hum Factors
Wan Y, Zhang Y, Zhao Y, Yu H, Liu K.
europepmc   +1 more source

EMBO Press co-evolves with molecular ecology and evolutionary biology. [PDF]

EMBO J
Moran Y, Coelho SM, Ettema TJG, Feschotte C, Kaltenpoth M, Khila A, Laine AL, Liow LH, Petrov D, Ramakrishnan U, Sarkies P, Srivastava M, Voolstra C, Pulverer B.   +13 more
europepmc   +1 more source