Results 211 to 220 of about 55,554 (300)

Serum glial fibrillary acidic protein and protein gene product 9.5 for predicting neurological outcomes in cardiac arrest patients with cortical response to somatosensory evoked potentials. [PDF]

Resusc Plus
Hang C, Shao R, Wang X, Zhang L, Cheng W, Jiang Z, Zhong Z, An L, Tang Z.   +8 more
europepmc   +1 more source

Immune‐Related Polyradiculoneuropathy Associated With Immune Checkpoint Inhibitors: A Comprehensive Case Series

Brain and Behavior, Volume 16, Issue 5, May 2026.
ABSTRACT Objective Immune‐related polyradiculoneuropathy (irPRN) is a rare but potentially severe neurological adverse event secondary to immune checkpoint inhibitors (ICIs), closely resembling Guillain–Barré syndrome. This study aims to characterize the clinical presentation, neurophysiological findings, therapeutic strategies, and clinical outcomes ...
A. Llauradó, E. Lainez, H. Ariño, M. Gratacòs‐Viñola, J. L. Seoane, M. Roca‐Herrera, J. L. Restrepo‐Vera, D. Sanchez‐Tejerina, N. Raguer, R. Juntas‐Morales   +9 more
wiley   +1 more source

Reduction of the acquisition time needed to obtain somatosensory evoked potentials by estimation of the required averaging sweep count by an algorithm. [PDF]

J Clin Monit Comput
Bothe C, Winterling C, Berndt K, Ahmeti H, Balandin A, Steinfath M, Helmers AK, Fudickar A.   +7 more
europepmc   +1 more source

Whole‐Brain Fractional Anisotropy, Centered on the Superior Longitudinal Fasciculus, Is Positively Correlated With Urban Aesthetic Perception

Brain and Behavior, Volume 16, Issue 5, May 2026.
This study examines the association between urban aesthetic perception and white matter microstructure in healthy adults. Diffusion tensor imaging reveals that both whole‐brain fractional anisotropy and superior longitudinal fasciculus integrity are positively related to subjective evaluations of urban aesthetic quality, suggesting that everyday ...
Keisuke Kokubun, Kiyotaka Nemoto, Maya Okamoto, Yoshinori Yamakawa   +3 more
wiley   +1 more source

A Chinese X‐Linked Adrenoleukodystrophy Patient With Atypical Clinical Symptoms Contained an Undefined ABCD1 Mutation—A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 5, May 2026.
ABSTRACT X‐linked adrenoleukodystrophy (X‐ALD) is a genetic peroxisome disorder linked to ABCD1 mutation, characterized by rapid and complex clinical symptoms. We here report a case of X‐ALD manifesting solely as dysarthria, associated with an undefined mutation in the ABCD1 gene, underscoring the necessity of atypical clinical symptoms in X‐ALD ...
Fu‐Qing Zhang, Zhuoran Zhang, Dongliang Wang, Ying Yang, Xin Li   +4 more
wiley   +1 more source

Time varying characteristic in somatosensory evoked potentials as a biomarker of spinal cord ischemic-reperfusion injury in rat. [PDF]

Front Neurosci
Li K, Yang J, Wang H, Chang X, Liu G, Xue R, Guo W, Hu Y.   +7 more
europepmc   +1 more source

Nerve conduction velocity in patients under longterm treatment with antiepileptic drugs [PDF]

, 1990
Berlit, Peter, Krause, Klaus-Henning
core  

Mechanistic Explanations of Manual Therapy Do Not Influence Outcomes in Healthy Individuals: A Randomized Controlled Trial

Health Science Reports, Volume 9, Issue 5, May 2026.
ABSTRACT Background and Aims Manual therapy is widely applied for musculoskeletal dysfunction and pain, yet the mechanisms underlying its effects remain incompletely understood. Local biomechanical and central neurophysiological processes are considered relevant, while contextual factors such as patient expectations and therapist beliefs may further ...
Sofie Waesch, Judith Leitner, Lisa M. Stelzer, Waclaw M. Adamczyk, Kerstin Luedtke, Tibor M. Szikszay   +5 more
wiley   +1 more source

Correction: Modulation of subjective peripheral sensation, F-waves, and somatosensory evoked potentials in response to unilateral pinch task measured on the contractile and non-contractile sides. [PDF]

PLoS One
Takahara T, Yamaguchi H, Seki K, Onodera S.   +3 more
europepmc   +1 more source

Complicated Spastic Paraparesis: Study of a Patient With a De Novo Pathogenic Variant in ELOVL1

International Journal of Developmental Neuroscience, Volume 86, Issue 3, May 2026.
A de novo ELOVL1 variant causes syndromic spastic paraparesis with congenital ichthyosis, cerebellar signs and white matter abnormalities. Long‐term clinical and MRI follow‐up showed mild motor and neuroradiological progression with preserved intelligence and subtle cognitive efficiency decline, supporting the hypothesis of a primary neuronal disease ...
Ylenia Vaia, Eleonora Mura, Fabio Bruschi, Stefania Zambrano, Michela Brena, Gianluca Tadini, Filippo Arrigoni, Clara E. Antonello, Carla Uggetti, Cecilia Parazzini, Pierangelo Veggiotti, Davide Tonduti   +11 more
wiley   +1 more source