Results 151 to 160 of about 10,132,612 (315)

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

The properties of panels in global comics: frequency and size of 76 K panels in 1,030 comics from 144 countries. [PDF]

open access: yesLang Resour Eval
Cohn N   +23 more
europepmc   +1 more source

Letter: Della Page French to Ida M. Tarbell, March 10, 1935

open access: yes, 1935
Handwritten letter.
French, Della Page
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Plasma EV Proteomics Identifies ECM Remodeling and Inflammatory Proteins LUM and C7 as Candidate Biomarkers in FSHD

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy (FSHD) is one of the most debilitating and common muscular dystrophies. Despite its severity, no approved therapy exists for FSHD patients. However, several therapeutic candidates are currently under development, and some have recently entered clinical trials, marking the need for reliable ...
Mustafa Bilal Bayazit   +11 more
wiley   +1 more source

Royalty Statements: Doubleday Page & Co. to Ida M. Tarbell, Febrary 1, 1909

open access: yes, 1909
Royalty Statements for works published by Doubleday Page & Co., February ...
Doubleday Page & Co.
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A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley   +1 more source

The use of an innovative clinical decision support system focused on psychosocial vulnerabilities during pregnancy: the Born in Belgium Professionals Platform. [PDF]

open access: yesBMC Health Serv Res
Amuli K   +14 more
europepmc   +1 more source

Toledo Calling

open access: yes, 2016
Toledo Calling was a bulletin published by B'Nai Women's Auxiliary Number 398. This monthly bulletin provided Toledo area happenings to Jewish men and women serving in the armed forces.
B'Nai Women's Auxiliary Number 398
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Evaluation of a Novel Electric Health Record Sidecar Application to Display Rheumatoid Arthritis Clinical Outcomes During Clinic Visits: Results of a Stepped‐Wedge Cluster Randomized Pragmatic Trial

open access: yesArthritis Care &Research, EarlyView.
Objective We developed a novel electronic health record sidecar application to visualize key rheumatoid arthritis (RA) outcomes, including disease activity, physical function, and pain, via a patient‐facing graphical interface designed for use during outpatient visits (“RA PRO dashboard”).
Gabriela Schmajuk   +16 more
wiley   +1 more source

Spiking neural models for decision-making tasks with learning. [PDF]

open access: yesJ Math Biol
Jaffard S   +3 more
europepmc   +1 more source

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