Results 31 to 40 of about 71,310 (254)

The Temporal Profiles of Changes in Nerve Excitability Indices in Familial Amyloid Polyneuropathy. [PDF]

PLoS ONE, 2015
Familial amyloid polyneuropathy (FAP) caused by a mutation in transthyretin (TTR) gene is an autosomal dominant inherited disorder. The aim of this study is to explore the pathophysiological mechanism of FAP.
Hsing-Jung Lai, Ya-Wen Chiang, Chih-Chao Yang, Sung-Tsang Hsieh, Chi-Chao Chao, Ming-Jen Lee, Chung-Chin Kuo   +6 more
doaj   +1 more source

Characterization of Parkinson's disease patients using individualized differential structural covariance network

Chinese Journal of Contemporary Neurology and Neurosurgery
Objective To investigate the individualized differential structural covariance network (IDSCN) in Parkinson's disease (PD) patients, and to examine their correlations with clinical symptoms.
QIN Xue-yan, MENG Xia-yu, WEI Shu-jie, DUAN Fei-yi, JI Yu-chen, MENG Fan-gang   +5 more
doaj   +1 more source

Research progress on the association between motor network and nervous system diseases

Chinese Journal of Contemporary Neurology and Neurosurgery
The motor network is a key system in the central nervous system responsible for motor control and coordination, and its dysfunction is closely associated with various nervous system diseases.
BAO Hong⁃bo, FANG Sheng⁃yu, WANG Yin⁃yan   +2 more
doaj   +1 more source

Maintenance and Regeneration of the Nerve Net in Hydra [PDF]

American Zoologist, 1988
Description des proprietes et de la dynamique du reseau nerveux. On observe comment ces proprietes sont impliquees dans la maintenance du reseau nerveux dans le contexte de la dynamique du tissu chez l'adulte ainsi que pendant le developpement du reseau nerveux au moment de la regeneration de la ...
H. R. BODE, S. HEIMFELD, O. KOIZUMI, C. L. LlTTLEFIELD, M. S. YAROSS   +4 more
openaire   +1 more source

Norepinephrine transporter variant A457P knock-in mice display key features of human postural orthostatic tachycardia syndrome

Disease Models & Mechanisms, 2013
SUMMARY Postural orthostatic tachycardia syndrome (POTS) is a common autonomic disorder of largely unknown etiology that presents with sustained tachycardia on standing, syncope and elevated norepinephrine spillover. Some individuals with POTS experience
Jana K. Shirey-Rice, Rebecca Klar, Hugh M. Fentress, Sarah N. Redmon, Tiffany R. Sabb, Jessica J. Krueger, Nathan M. Wallace, Martin Appalsamy, Charlene Finney, Suzanna Lonce, André Diedrich, Maureen K. Hahn   +11 more
doaj   +1 more source

Cnidarian Nerve Nets and Neuromuscular Efficiency [PDF]

Integrative and Comparative Biology, 2015
Cnidarians are considered "nerve net animals" even though their nervous systems include various forms of condensation and centralization. Yet, their broad, two-dimensional muscle sheets are innervated by diffuse nerve nets. Do the motor nerve nets represent a primitive organization of multicellular nervous systems, do they represent a consequence of ...
openaire   +2 more sources

Radioterapi Eksternal terhadap Nilai Ambang Eksitabilitas Saraf Fasialis pada Radioterapi Eksternal Penderita Karsinoma Nasofaring

Majalah Kedokteran Bandung, 2013
External radiotherapy is the main treatment for nasopharyngeal carcinoma. One of complication of the external beam radiotherapy (EBRT) is peripheral neuropathy.
Yunaldi Altila, Dindy Samiadi, Nur Akbar Aroeman   +2 more
doaj   +1 more source

Fully automated preoperative segmentation of temporal bone structures from clinical CT scans

Scientific Reports, 2021
Middle- and inner-ear surgery is a vital treatment option in hearing loss, infections, and tumors of the lateral skull base. Segmentation of otologic structures from computed tomography (CT) has many potential applications for improving surgical planning
C. A. Neves, E. D. Tran, I. M. Kessler, N. H. Blevins   +3 more
doaj   +1 more source

Sustained Therapeutic Efficacy of Intravenous Plasminogen Concentrate in Pediatric Patients With Type 1 Plasminogen Deficiency: An Analysis of Dosing Parameters and Clinical Outcomes

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Type 1 plasminogen deficiency (PLGD‐1) is an ultra‐rare autosomal recessive disorder caused by variants in the PLG gene and affects approximately 1.6 individuals per million. The condition is characterized by decreased plasminogen levels and impaired function, resulting in fibrin‐rich lesions on mucous membranes throughout the body.
Charles Nakar, Karen Thibaudeau, Mary Mathias, Heather McDaniel, Madlen Reschke, Klaus Tenbrock, Joseph M. Parker, Amy Shapiro   +7 more
wiley   +1 more source

Distinguishing Interictal Neuromagnetic Activity in Migraine With and Without Aura: A Resting-State Magnetoencephalography Study

Journal of Integrative Neuroscience
Background: Migraine with aura (MwA) and migraine without aura (MwoA) are believed to have distinct pathophysiological mechanisms. However, differences in their neuromagnetic activity are currently unclear.
Di Wu, Hongxing Liu, Zhiyuan Zhou, Yuanwen Yu, Qiqi Chen, Xiaoshan Wang   +5 more
doaj   +1 more source