Results 181 to 190 of about 5,167 (227)

Advancing APT detection through transformer-driven feature learning and synthetic data generation. [PDF]

Sci Rep
Danh LTK, Xuan CD, Van NN.
europepmc   +1 more source

Spatial and Volumetric Characteristics of Glioblastoma: Associations With Clinical Presentation and Survival

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We aim to comprehensively analyze how regional tumor and edema characteristics are associated with clinical presentations and survival outcomes in a large cohort of glioblastoma patients. Methods Patients with IDH‐wildtype glioblastoma who received brain MRI from 2010 to 2023 were included.
Daniel J. Zhou, Marc Jaskir, Julian Gal, Yombe Fonkeu, Christos Davatzikos, MacLean P. Nasrallah, Jose Garcia, Rubo Xing, Stephen J. Bagley, Arati Desai, Richard E. Phillips, Steven Tobochnik, Colin A. Ellis, James J. Gugger, Nishant Sinha, Joel M. Stein, Kathryn A. Davis   +16 more
wiley   +1 more source

An intelligent diagnosis method for PMSM radial misalignment based on current signal and Swin-BiGRU multimodal fusion. [PDF]

Sci Rep
Yu H, Guo J, Zhang H.
europepmc   +1 more source

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

Annals 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, Akansha Chandrasekar, Kyla Blasingame, Jonathan Rosen, Jesse M. Levine, Karla Salazar, Madhuri Chilakapati, Rod Foroozan, Victoria Hardwick, Jonathan M. Yarimi, Nikita Shukla, Timothy E. Lotze, Kristen S. Fisher, Alexander J. Sandweiss   +13 more
wiley   +1 more source

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

Annals 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, Dong‐Lin Liang, Li‐Ping Gao, Wei‐Wei Zhang, Wei Zhou, A. Ruhan, Bing Xu, Run‐Dong Cao, Kang Xiao, Cao Chen, Qi Shi, Xiao‐Ping Dong   +11 more
wiley   +1 more source

An explainable streaming early identification model for early neurological deterioration based on coordinated fusion of ECG waveforms and vital signs. [PDF]

Front Neurol
Zhang Y, Yao S, Wen B, Liu J.
europepmc   +1 more source

Label-free multiphoton microscopy of human skin: longitudinal studies capturing cell dynamics. [PDF]

Biomed Opt Express
Vallmitjana A, Durkin A, Dvornikov A, Torrado B, Kelly KM, Shiu J, Ganesan AK, Balu M.   +7 more
europepmc   +1 more source

Blood-based proteomic signature of amyloidosis: identification of novel regulators of amyloid load. [PDF]

Alzheimers Dement
Chen Y, Duggan MR, Timsina J, Xu Y, Western D, Gong K, Liu M, Budde J, Schindler SE, Morris JC, Holtzman DM, Benzinger TLS, Gordon BA, Moqri M, Knight Alzheimer Disease Research Center (Knight‐ADRC), Ibanez L, Walker KA, Cruchaga C, Ali M.   +18 more
europepmc   +1 more source

Molecular and Functional Platelet Abnormalities in Myeloproliferative Neoplasms. [PDF]

Cells
Wang AX, Guo BB, Linden MD.
europepmc   +1 more source

Quantitative Profiling of Nanoscopic Protein Aggregates Reveals Specific Fingerprint of TDP-43-Positive Assemblies in Motor Neuron Disease. [PDF]

Adv Sci (Weinh)
Cox D, Burke M, Milani S, White MA, Waldron FM, Böken D, Lobanova E, Sreedharan J, Gregory JM, Klenerman D.   +9 more
europepmc   +1 more source