Results 81 to 90 of about 15,154 (201)

Diagnostic Performance of the Strength‐Duration Test for Bedside Screening of Critical Illness Polyneuropathy and/or Myopathy: A Prospective, Cross‐Sectional Study

Muscle &Nerve, Volume 74, Issue 4, Page 1212-1219, October 2026.
ABSTRACT Introduction/Aims Critical illness polyneuropathy and/or myopathy (CIP/CIM) is a major cause of weakness in the intensive care unit (ICU). The availability of conventional electrodiagnostic testing may be limited. Alternative electrophysiologic methods, including the strength‐duration test (SDT) and the stimulus electrodiagnosis test (SET ...
José Roberto de Deus Macedo, Emerson Fachin‐Martins, Marilia Mendes Rodrigues, Marta Rodrigues de Carvalho, Rubens Nelson Morato Fernandez, Paulo Eugênio Silva   +5 more
wiley   +1 more source

CMap additional data/files

The additional files for the major revision of Cell lineage-resolved embryonic morphological map reveals novel signaling regulating cell fate and size asymmetry (https://www.researchsquare.com/article/rs-4664717/v1)
Zelin Li, Guoye Guan
openaire   +1 more source

Revisiting the compound muscle action potential (CMAP)

Clinical Neurophysiology Practice
The compound muscle action potential (CMAP) is among the first recorded waveforms in clinical neurography and one of the most common in clinical use. It is derived from the summated muscle fiber action potentials recorded from a surface electrode overlying the studied muscle following stimulation of the relevant motor nerve fibres innervating the ...
Paul E. Barkhaus, Sanjeev D. Nandedkar, Mamede de Carvalho, Michael Swash, Erik V. Stålberg   +4 more
openaire   +3 more sources

Optimal Hypoxia Mimetic Small Molecules for Enhancing Angiogenic Properties of Stem Cells From Human Exfoliated Deciduous Teeth

International Endodontic Journal, Volume 59, Issue 10, Page 2122-2142, October 2026.
ABSTRACT Aim Hypoxic preconditioning of cells holds promise for regenerative therapies, yet identifying effective and safe methods for clinical application remains challenging. We aimed to determine optimal hypoxia‐mimetic small molecules (SMs) that stabilize hypoxia‐inducible factor‐1α (HIF‐1α) and their dosages for hypoxic preconditioning in stem ...
Hong Wang, Jiawei Liu, Xintao Yang, Mohamad Koohi‐Moghadam, Shuting Gao, Yuanyuan Han, Dineshi Sewvandi Thalakiriyawa, James Kit Hon Tsoi, Yanqi Yang, Waruna Lakmal Dissanayaka   +9 more
wiley   +1 more source

Integrative Transcriptomic Profiling Delineates LTBP4‐Driven Fibroblast Reprogramming Across the Ossification Continuum of the Ligamentum Flavum

The FASEB Journal, Volume 40, Issue 17, 15 September 2026.
This study delineates the dynamic transcriptomic landscape of OLF across normal, immature, and mature stages via RNA‐seq. LTBP4 shows progressive downregulation and is validated in external datasets. Single‐cell and spatial transcriptomics identify fibroblasts as the cellular source.
Xiao Zhang, Tengyao Niu, Yulong Zhao, Zhenguo Liu, Wenbo Gu, Donghui Cao, Yanrong Tian, Haifeng Yuan   +7 more
wiley   +1 more source

mdashkezari/cmap-agent-paper: CMAP Agnet Paper

Reference repository for CMAP agent CMAP Agent document project. The paper introduces an agentic retrieval-augmented interface for dataset discovery, access, integration, and analysis on Simons CMAP data platform.
openaire   +1 more source

Monoallelic POLR3A Variants Cause Early‐Onset Peripheral Neuropathy

Annals of Neurology, Volume 100, Issue 3, Page 655-671, September 2026.
Objective Biallelic variants in genes encoding the RNA polymerase III complex (Pol III) cause a spectrum of neurological disorders primarily affecting the central nervous system. Monoallelic variants have been reported in the POLR3B subunit only, associated with neurodevelopmental disorder, epilepsy, and peripheral neuropathy.
Luiza L. P. Ramos, Jevin M. Parmar, Robin Wijngaard, Bianca R. Grosz, Tamas Lazar, Ligia Mateiu, Steve Vucic, Kishore R. Kumar, Dennis Yeow, Laura I. Rudaks, Lonneke de Boer, Annemarie de Vreugd, David A. Koolen, Thatjana Gardeitchik, Anita Cairns, Krishnan Iyengar, Fernando Kok, Fernanda Barbosa Figueiredo, Alzira Alves de Siqueira Carvalho, Luiz S. Mageste Barbosa, Rodrigo Rezende Arantes, Tyler Rehbein, Jordan E. Bontrager, Elizabeth P. Wood, Janet E. Sowden, Gavin Monahan, Meutia Kumaheri, Ivy Cuijt, Melina Ellis, Gonzalo Perez‐Siles, Elyshia McNamara, Ronald van Beek, Celine B. Meijers, Ivaylo Tournev, Stephan Zuchner, Shoshana J. Wodak, Clara D. M. van Karnebeek, Nigel Laing, Liana N. Semcesen, David A. Stroud, David N. Herrmann, Velina Guergueltcheva, Marina L. Kennerson, Machteld M. Oud, Gianina Ravenscroft, Ayse Candayan, Albena Jordanova   +46 more
wiley   +1 more source

Maternal‐Fetal Administration of Risdiplam Partially Rescues the SMNΔ7 Mouse Model of Spinal Muscular Atrophy

Annals of Neurology, Volume 100, Issue 3, Page 584-599, September 2026.
Objective Spinal muscular atrophy (SMA) is caused by deletions or mutations in the survival motor neuron 1 (SMN1) gene and subsequent reduction in the expression of survival motor neuron (SMN) protein. The disease is characterized by degeneration of α motor neurons and subsequent muscle atrophy.
Emma R. Sutton, Ariane Beauvais, Rebecca Yaworski, Hugh J. McMillan, Rashmi Kothary   +4 more
wiley   +1 more source

Bridging Theory and Practice: Digital Twin Simulation of a Heat Exchanger in Laboratories for Engineering Students

Computer Applications in Engineering Education, Volume 34, Issue 5, September 2026.
ABSTRACT Digital twins serve as virtual replicas of physical systems. They can be used as a tool for engineering education by revealing the underlying principles behind unit operations. The project aimed to integrate digital twins into university engineering lab courses, complementing traditional methods by bridging the gap between experimentation and ...
Carles Troyano Ferré, Ruben Cabello, Pau Folch‐Millán, Alexandra Elena Plesu Popescu, Jordi Bonet Ruiz, Roger Bringué Tomàs   +5 more
wiley   +1 more source

Unexpected Conduction Blocks in SORD‐Related Distal Motor Neuropathy: A Case Report

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Distal weakness requires an extensive differential diagnosis. In this case, conduction blocks indicated multifocal motor neuropathy, but immunotherapy proved ineffective. Ultimately, genetic testing revealed a sorbitol dehydrogenase mutation, highlighting the importance of combining electrophysiological findings with molecular studies in cases
Amiela Angeli Bucur, Gabriele Rodolico, Alessandra Tessa, Filippo Maria Santorelli, Martina Sperti, Deborah Leccese, Mario Maturo, Sabrina Matà   +7 more
wiley   +1 more source