Results 131 to 140 of about 1,191,200 (300)
Evaluation of Translucency, Chroma, Value in Some Commercial Dental Resin Composites
Introduction: Optical properties of different resin composites may affect the correspondence between tooth color and its structure. Therefore, this study aimed to evaluate and compare the optical properties of 8 commercial composite resin materials with ...
AR Daneshkazemi +3 more
doaj
Dimethyl Fumarate, But Not Rituximab, Reduces Serum GFAP Levels and PIRMA in Relapsing–Remitting MS
ABSTRACT Objective Serum neurofilament light chain (sNfL) and glial fibrillary acidic protein (sGFAP) levels are believed to reflect mainly acute and chronic disease processes in multiple sclerosis (MS), respectively. In this study, we investigated whether dimethyl fumarate (DMF) and rituximab (RTX) differentially affect these biomarkers.
F. Shawket +14 more
wiley +1 more source
Aquaporin‐4 in Narcolepsy Type 1: Investigation of Perivascular Fluid Movement in Sleep Disorders
ABSTRACT Narcolepsy type 1 (NT1) is caused by the loss of hypocretin‐1 leading to excessive daytime sleepiness and cataplexy. Additionally, disrupted nighttime sleep has become an increasingly recognized feature of NT1. As the glymphatic fluid movement has been linked to sleep architecture, we investigated cerebrospinal fluid (CSF) Aquaporin‐4 (AQP4 ...
Jonas Ranke +5 more
wiley +1 more source
VPRS 12734 Secretary's Correspondence Action Book, Commercial Branch
The Department of Railways was organised into various branches, each with its own separate registry and record-keeping systems dealing with its own activities and administration.<br/><br/>Within each Division an officer was responsible for ...
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This is an item from the William Crawford Gorgas Papers. This collection includes material created by and written about Gorgas, as well as material created by Gorgas' family members.
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Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach +23 more
wiley +1 more source
Correspondence with potential and actual corporate sponsors
During this period the Legal Information Institute offered commercial publishers the trade of a day of consulting by Martin and Bruce in return for financial sponsorship.
Martin, Peter
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Persistent Bilateral [18F]THK5351 and Migrating Unilateral [18F]FDG Uptake in Anti‐LGI1 Encephalitis
ABSTRACT Anti–leucine‐rich glioma‐inactivated 1 encephalitis (LGI1‐E) can cause persistent cognitive deficits, but the mechanisms remain unclear. A 40‐year‐old woman with LGI1‐E presented with subacute cognitive deficits and showed mild left medial temporal lobe (MTL) swelling and fluid‐attenuated inversion recovery (FLAIR) hyperintensity on initial ...
Yusuke Akitomi +8 more
wiley +1 more source
PhDThe years after 1763 were vital to the special position of the West Indian islands within the British Empire. Yet no integrated study has been made of the economic and political issues raised in the West Indies during the period of the confrontation ...
Carrington, Selwyn Hawthorne Hamilton
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Comparative Effectiveness and Safety of Inebilizumab Versus Rituximab in AQP4‐IgG‐Positive NMOSD
ABSTRACT Objective Rituximab (anti‐CD20, RTX) and inebilizumab (anti‐CD19, INE) represent B‐cell‐depleting therapies used for aquaporin‐4 antibody‐positive (AQP4‐IgG+) neuromyelitis optica spectrum disorder (NMOSD); however, direct comparative evidence remains limited.
Jie Lin +11 more
wiley +1 more source

