Results 61 to 70 of about 4,424 (197)

Backpropagation Network‐Based Contrastive Learning for Unsupervised Domain Adaptation

Engineering Reports, Volume 8, Issue 6, June 2026.
Unsupervised domain adaptation for contractive learning. ABSTRACT This study introduces a new method for domain adaptation for image classification tasks that aims to improve the model's performance on a target domain after being trained on a source domain.
Yushui Xiao, Yong Huang, Yujie Li
wiley   +1 more source

Visual evoked potential in generalized joint hypermobility: A case–control study

Brain and Behavior
Introduction Generalized joint hypermobility (GJH) can be the result of several hereditary connective tissue disorders, especially Ehlers–Danlos syndrome.
Leila Sadat Mohamadi Jahromi, Amin Sayyadi, Aida Askarian, Alireza Dabbaghmanesh, Sharareh Roshanzamir   +4 more
doaj   +1 more source

valuation of Subclinical Multiple Sclerosis Patients Using Pattern Visual Evoked Potentials and Visual Field Test

Türk Oftalmoloji Dergisi, 2014
Objectives: The aim of this study was to evaluate subclinical multiple sclerosis (MS) patients with normal visual acuity using pattern visual evoked potentials (PVEP) test and central 30-2 threshold visual field (VF) test.
Sinan Bilgin, Süleyman Sami İlker, Ercüment Çavdar   +2 more
doaj   +1 more source

The NF‐κB Signalling Pathway: Mechanisms, Consequences and Therapeutic Targets

Journal of Cellular and Molecular Medicine, Volume 30, Issue 11, June 2026.
ABSTRACT Nuclear Factor‐kappa B (NF‐κB) is a master transcriptional regulator orchestrating critical cellular processes, predominantly immunity and inflammation. However, its aberrant constitutive activation has emerged as a unifying pathogenetic hallmark across diverse malignancies, autoimmune disorders, and chronic inflammatory diseases.
Bherouz Pourdad, Arash Pourdad
wiley   +1 more source

Integrating Artificial Intelligence With Droplet‐Based Microfluidics: Advances, Challenges, and Emerging Opportunities

Advanced Intelligent Systems, Volume 8, Issue 5, May 2026.
Droplet‐based microfluidics enables precise, high‐throughput microscale reactions but continues to face challenges in scalability, reproducibility, and data complexity. This review examines how artificial intelligence enhances droplet generation, detection, sorting, and adaptive control and discusses emerging opportunities for clinical and industrial ...
Junyan Lai, Sukrit Gaira, Rongfeng Wang, Qingtian Zhang, Ming Li, Liao Wu, Diangeng Li, Yi Li, Chengchen Zhang, Jinhong Guo, Shi‐Yang Tang   +10 more
wiley   +1 more source

Case Report of Combined Central and Peripheral Demyelination: Treated With Ofatumumab

Immunity, Inflammation and Disease, Volume 14, Issue 5, May 2026.
ABSTRACT Background and Objectives Combined central and peripheral demyelination (CCPD) is a rare autoimmune‐mediated disorder characterized by demyelination affecting both the central nervous system and peripheral nervous system. The involvement of the CNS typically manifests as longitudinally extensive transverse myelitis and optic neuritis, whereas ...
Lili Liu, Zhigang Zhong, Haijun Wu, Jun Hu, Juanjuan Chen   +4 more
wiley   +1 more source

Is the P300 deficit in alcoholism associated with early visual impairments (P100, N170)? An oddball paradigm.

, 2007
OBJECTIVE: Studies exploring chronic alcoholism with event-related potentials (ERPs) have shown delayed latency and reduced amplitude of the P300, a long-lasting positive potential reflecting decisional processing.
Kornreich, C, Maurage, Pierre, Hanak, Catherine, Noel, X, Verbanck, P., Verbanck, Paul, Noël, Xavier, Philippot, P, Maurage, P, Philippot, Pierre, Kornreich, Charles, Campanella, Salvatore, Hanak, C   +12 more
core   +1 more source

Novel LAMA1 Mutations in a Pedigree With Poretti‐Boltshauser Syndrome: Implications for Hypomyelination

Molecular Genetics &Genomic Medicine, Volume 14, Issue 5, May 2026.
This study reports novel compound heterozygous LAMA1 variants in two siblings with Poretti‐Boltshauser syndrome presenting with cerebral hypomyelination. It provides the first clinical evidence linking LAMA1 to CNS dysmyelination, expanding the phenotypic spectrum and offering mechanistic insights into this rare association. ABSTRACT Background Poretti‐
Si Huang, Yiyang Li, Jing Xin, Wenhui Mo, Xiuwen Lin, Bingbin Mai, Junbin He, Xiaoli Zhong, Jiaxin Xu   +8 more
wiley   +1 more source

Reversible cerebral and brain stem dysfunction in n: Hexane neuropathy

Annals of Indian Academy of Neurology, 2015
A 18-year-old male, screen printer by profession developed sensory motor polyneuropathy, change in his behavior, bilateral 6 th and 7 th cranial nerve palsies, down beat nystagmus and cerebellar dysarthria. He had bilaterally prolonged P100 latency; left:
Vinod Puri, Abhijit Das Gupta, Neera Chaudhry, Ravindra Kumar Saran   +3 more
doaj   +1 more source

Homozygous Pathogenic Variant in Elongation Factor‐Like 1 (EFL1) as a Causal Factor in Shwachman‐Diamond Syndrome 2 in a Palestinian Child, With Distinct Ocular Manifestations

Molecular Genetics &Genomic Medicine, Volume 14, Issue 5, May 2026.
We report a Palestinian female infant with a homozygous pathogenic EFL1 variant (c.3284G>A; p.Arg1095Gln) causing Shwachman–Diamond syndrome type 2 (SDS2). Beyond the classical features of pancytopenia, exocrine pancreatic insufficiency, and growth failure, the patient showed previously unreported ocular manifestations—stage 2–3 retinopathy of ...
Ibrahim Taha, Antonella Minelli, Cesare Danesino, Abdelrahman Swalmeh, Khalil Huraibat, Liana Al‐Labadi, Rema Obar, Khaled R. Beshtawi, Lubna Abu Samrah, Yousef Awlad Mohammad, Aya Farah, Abdulrahman Obar, Mutasem Khalaf, Orwa Nasser   +13 more
wiley   +1 more source