Results 271 to 280 of about 48,300 (324)

Wireless Capsule Device for Targeted and Safe Tissue Biopsy with Integrated Sensing

Advanced Materials Technologies, Volume 10, Issue 23, December 3, 2025.
This work presents a capsule device featuring a novel magnetically controlled biopsy mechanism for enhanced safety. The biopsy unit integrates a foldable linkage with dual magnets, creating a magnetic attraction–based safeguard, preventing unintended activation during locomotion. A flexible sensor provides real‐time penetration displacement sensing for
Kiyoung Kim, Jacob Katona, Jiale Chu, Boyang Xiao, Rishi Naik, Xiaoguang Dong   +5 more
wiley   +1 more source

Advancing Clinical Medicine with Raman Spectroscopy: Current Trends and Future Perspectives

Advanced Photonics Research, Volume 6, Issue 12, December 2025.
Raman spectroscopy and microscopy may become excellent tools in clinical medicine, including hematology, oncology, infectious diseases, neurology, gastroenterology, reproductive medicine, rheumatology, and cardiovascular research. However, many challenges such as signal interference, standardization issues, and limited clinical application need to be ...
Jiří Bufka, Lenka Vaňková, Josef Sýkora, Věra Křížková, Jan Schwarz, Petr Bouř   +5 more
wiley   +1 more source

Limitations of Faecal Calprotectin in Detecting Histological Changes and Persistent Villous Atrophy in Patients With Coeliac Disease on a Gluten-Free Diet. [PDF]

Aliment Pharmacol Ther
Segura V, Ruiz-Carnicer Á, Pizarro Á, González-Naranjo C, Díaz J, Coronel-Rodríguez C, Argüelles-Arias F, Garzón-Benavides M, Sousa C, Comino I.   +9 more
europepmc   +1 more source

Integrating Single‐Cell Transcriptome‐Wide Mendelian Randomization and Differentially Expressed Gene Analyses to Prioritize Dynamic Immune‐Related Drug Targets for Cancers

Advanced Science, Volume 12, Issue 46, December 11, 2025.
Inspired by evidence triangulation, a new sensitivity method called MR‐DEG is developed, which uses the differentially expressed gene (DEG) results as additional evidence to minimize pleiotropic effects and strengthen Mendelian randomization (MR) causal estimates. Using dynamic single‐cell expression quantitative trait loci (eQTLs) as an example, it is
Jie Zheng, Qian Yang, Haoyu Liu, Huiling Zhao, Shuangyuan Wang, Yi Liu, Xueyan Wu, Yilan Ding, Hui Ying, Youqiu Ye, Xi Huang, Lei Ye, Ruizhi Zheng, Hong Lin, Mian Li, Tiange Wang, Zhiyun Zhao, Min Xu, Yi Duan, Hao Guo, Zhongshang Yuan, Philip Haycock, George Davey Smith, Richard M Martin, Guang Ning, Fang Hu, Weiqing Wang, Tom R. Gaunt, Jieli Lu, Yufang Bi   +29 more
wiley   +1 more source

Evolution in coeliac disease diagnosis and management. [PDF]

JGH Open
Tye-Din JA.
europepmc   +1 more source

Early Enzyme Replacement Therapy Does Not Prevent the Protein Losing Enteropathy Syndrome in Neurovisceral Gaucher Disease

American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Gaucher disease (GD) is a rare lysosomal storage disorder characterized by multisystemic involvement. With the advent of enzyme replacement therapy (ERT), patient survival has improved, revealing new long‐term complications. We report a case of a 4‐year‐old male with severe neurovisceral GD who developed protein‐losing enteropathy (PLE ...
Vincenza Gragnaniello, Mara Cananzi, Annachiara Cavaliere, Christian Loro, Chiara Cazzorla, Daniela Gueraldi, Andrea Puma, Alberto B. Burlina   +7 more
wiley   +1 more source

Life Challenges and Quality of Life of People Living With Coeliac Disease: Time of Diagnosis Matters. [PDF]

J Hum Nutr Diet
Stroebele-Benschop N, Rau CJ, Dieze A, Bschaden A.   +3 more
europepmc   +1 more source

Abdominal Sarcoidosis: A Mystery Revisited

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Unexplained lymphadenopathy is an often‐encountered symptom or abnormal finding during physical examinations in practice, and it can stem from a wide range of causes. These require multiple investigations to reach a diagnosis. One of the rare causes is Sarcoidosis, which is a multi‐system disease characterized by the infiltration of various ...
Lovenish Bains, Nidhi Paswan, Soukat Ali Khan, Shramana Mandal   +3 more
wiley   +1 more source

Coeliac Disease in Children-A Clinical Review Including Novel Treatment Agents. [PDF]

Medicina (Kaunas)
Corlett C, Rodrigues A, Ravikumara M.
europepmc   +1 more source

Comorbidity of Attention Deficit Hyperactivity Disorder (ADHD) and Chung‐Jansen Syndrome: Case Report and Review of Literature

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Chung‐Jansen Syndrome (CJS) is a rare autosomal dominant neurodevelopmental disorder caused by heterozygous mutations in the PHIP gene (6q14.1). It is characterized by developmental delay, intellectual disability, behavioral disturbances including autism spectrum disorder and attention deficit hyperactivity disorder, obesity, and distinct ...
Maedeh Khalili, Maryam Yousefi Fahadani, Reza Bidaki, Zahra Talayi   +3 more
wiley   +1 more source