Results 141 to 150 of about 586 (259)

Characterizing Combined Central and Peripheral Demyelination—Insights From a Multimodal Comparison With Chronic Inflammatory Demyelinating Polyneuropathy and Multiple Sclerosis

open access: yesMuscle &Nerve, Volume 74, Issue 3, Page 605-615, September 2026.
ABSTRACT Introduction/Aims Combined central and peripheral demyelination (CCPD) is a rare dysimmune disorder sharing features with multiple sclerosis (MS) and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Direct comparisons of central and peripheral diagnostic findings across these entities remain limited. We, therefore, performed a
N. Dubuisson   +6 more
wiley   +1 more source

Quantification of the Tissue Sodium Concentration in the Human Calf at 7T With Reduced Acquisition Time: Influence of the Nominal Spatial Resolution

open access: yesNMR in Biomedicine, Volume 39, Issue 9, September 2026.
Fast 23Na MRI of the human calf at 7T was achieved by reducing nominal spatial resolution. Shorter measurement times can improve clinical feasibility of 23Na MRI while preserving reliable quantification of apparent tissue sodium concentration through partial volume, relaxation, and B0/B1 corrections.
Jordan M. Höhn   +6 more
wiley   +1 more source

A New Species of Loxomerus Chaudoir (Coleoptera: Carabidae: Migadopinae) From the Subantarctic Antipodes Islands, New Zealand: Resurgence of a Flightless Beetle Following Mouse Eradication

open access: yesNew Zealand Journal of Zoology, Volume 53, Issue 3, September 2026.
Loxomerus antipodes Liebherr and Marris, sp. nov. (Coleoptera: Carabidae), is described from the New Zealand subantarctic Antipodes Islands archipelago. Loxomerus antipodes, sp. nov., was considered conspecific with Loxomerus brevis Blanchard, 1853, from the Auckland Islands, but it is diagnosed from that sister taxon based on numerous anatomical ...
John W. M. Marris   +2 more
wiley   +1 more source

Optical mapping reveals a higher level of large‐scale structural variants in a family with paternally transmitted myotonic dystrophy and independent Parkinson's disease

open access: yesThe Journal of Pathology, Volume 270, Issue 1, Page 83-97, September 2026.
Abstract Myotonic dystrophy type 1 (DM1) is a clinically challenging multisystem neuromuscular hereditary disorder, with generational increase in severity and earlier age at onset. It is caused by an unstable cytosine‐thymine‐guanine repeat expansion at the DMPK locus, accompanied by associated genetic and epigenetic modifications.
Md Mehedi Hasan   +9 more
wiley   +1 more source

Bionic Tactile Skins for Robotics: Fundamentals, Advances, and Future Prospects

open access: yesSmartSys, Volume 2, Issue 3, September 2026.
ABSTRACT Robotic bionic tactile skins (RBTSs), as crucial components of next‐generation robotic systems, have attracted significant attention in recent years. By enabling robots to achieve human‐like tactile perception and interact effectively with their surroundings, RBTSs play an essential role in enhancing robotic intelligence.
Jiajun Wu   +8 more
wiley   +1 more source

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