Results 191 to 200 of about 1,521,521 (318)
A New Upper Bound on Total Domination Number of Bipartite Graphs [PDF]
Saieed Akbari +4 more
openalex +1 more source
ABSTRACT Background Neurodegeneration with brain iron accumulation (NBIA) comprises a genetically and clinically heterogeneous group of rare neurological disorders characterized particularly by iron accumulation in the basal ganglia. To date, 15 genes have been associated with NBIA.
Seda Susgun +95 more
wiley +1 more source
TGN-MCDS: A Temporal Graph Network-Based Algorithm for Cluster-Head Optimization in Large-Scale FANETs. [PDF]
Fan X, Yang Y, Zhang S, Cai W.
europepmc +1 more source
Decreased Serum 5‐HT: Clinical Correlates and Regulatory Role in NMJ of MG
ABSTRACT Objective Although 5‐Hydroxytryptamine (5‐HT) indirectly stimulates muscle contraction and participates in regulating Acetylcholine receptor (AChR) cluster homeostasis in cellular, animal, and clinical studies, evidence regarding its potential to modulate muscle contraction in myasthenia gravis (MG) remains limited.
Xinru Shen +18 more
wiley +1 more source
Associations Between Peer Victimization and Aggression and Three Types of Domestic Violence in Adolescents with Attention-Deficit/Hyperactivity Disorder. [PDF]
Lin PC, Tsai CS, Hsiao RC, Yen CF.
europepmc +1 more source
ABSTRACT Background Apolipoprotein ε4 (APOE ε4) is a potent genetic risk factor for Alzheimer's disease (AD). However, its role in cerebral small vessel disease (CSVD) remains unclear. Given the clinical and pathological similarities between CSVD and AD, this study aimed to investigate the associations of APOE ε4 gene dosage with cognitive function and
Tingru Jin +6 more
wiley +1 more source
Vertex colorings resulting from proper total domination of graphs [PDF]
Sawyer Osborn, Ping Zhang
doaj +1 more source
Bloodstream infection by Lactobacillus rhamnosus in a haematology patient: why metagenomics can make the difference. [PDF]
Mannavola CM +8 more
europepmc +1 more source
ABSTRACT Pathogenic variants in KIF1C cause Spastic Paraplegia 58 (SPG58), typically presenting with cerebellar ataxia and spastic paraparesis. We report two unrelated patients with spastic paraparesis, cerebellar ataxia, and tremor. Whole‐exome sequence analysis identified novel homozygous variants in the motor domain of KIF1C (NM_006612.6): c.921G>A (
Akihiko Mitsutake +12 more
wiley +1 more source
Studying Evolutionary Solution Adaption by Using a Flexibility Benchmark Based on a Metal Cutting Process. [PDF]
Dal Piccol Sotto LF +4 more
europepmc +1 more source

