Results 91 to 100 of about 5,204,108 (294)

Long‐Term Follow‐Up of Chemotherapy‐Associated Biological Aging in Women With Early Breast Cancer

open access: yesAging and Cancer, EarlyView.
Women threated with adjuvant chemotherapy for early breast cancer have sustained long‐term increase in p16INK4a,, a robust marker of cell senescence, suggesting a chemotherapy‐associated age acceleration. p16INK4a as well as other biomarkers may identify patients at greatest risk for senescence‐related diseases of aging.
Hyman B. Muss   +12 more
wiley   +1 more source

Soft Rough Approximation Operators and Related Results

open access: yesJournal of Applied Mathematics, 2013
Soft set theory is a newly emerging tool to deal with uncertain problems. Based on soft sets, soft rough approximation operators are introduced, and soft rough sets are defined by using soft rough approximation operators.
Zhaowen Li, Bin Qin, Zhangyong Cai
doaj   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

A novel algorithmic multi-attribute decision-making framework for the evaluation of energy systems using rough approximations of hypersoft sets

open access: yesHeliyon
Selecting the best power source that is legal, affordable, environmentally friendly, and able to ensure long-term viability is a difficult but vital task.
Muhammad Abdullah   +3 more
doaj   +1 more source

Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos   +5 more
wiley   +1 more source

Three-Way Approximations with Covering-Based Rough Set

open access: yesAxioms
In order to approximate an undefinable set of objects by using the extensions in OE-concept lattices, this study combines three-way concept analysis with covering-based rough set and introduces an innovative approach for managing uncertain information ...
Mei Li, Renxia Wan
doaj   +1 more source

Approximation of Rough Soft Set and Its Application to Lattice

open access: yesFuzzy Information and Engineering, 2015
The approximation of soft set is presented in modified soft rough (MSR) approximation space in this paper, i.e., approximation of an information system with respect to another information one.
Sankar Kumar Roy, Susanta Bera
doaj   +1 more source

Advances in fuzzy sets and rough sets

open access: yesInternational Journal of Approximate Reasoning, 2006
n ...
Masulli, F., Petrosino, A.
openaire   +2 more sources

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

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

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