Results 211 to 220 of about 308,175 (358)

Diffusion Spectrum Imaging Maps Early Axonal Loss and a Unique Progressive Signal in Neuronal Intranuclear Inclusion Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To delineate specific in vivo white matter pathology in neuronal intranuclear inclusion disease (NIID) using diffusion spectrum imaging (DSI) and define its clinical relevance. Methods DSI was performed on 42 NIID patients and 38 matched controls.
Kaiyan Jiang, Yixiu Pei, Xiaobao Hu, Ying Xiong, Fang Wang, Yanyan Yu, Min Zhu, Dandan Tan, Meihong Zhou, Daojun Hong, Fuqing Zhou   +10 more
wiley   +1 more source

The adiponectin/leptin ratio as a biomarker of adiposopathy and visceral adipose tissue accumulation: sex-specific mechanisms. [PDF]

Adipocyte
Medina-Urrutia A, Torre-Villalvazo I, Díaz-Villaseñor A, Jorge-Galarza E, Cervantes-Pérez LG, Antonio-Villa NE, Santibañez-Escobar F, Leal-Escobar G, Marquina-Castillo B, Martínez-Sánchez FD, Juárez-Rojas JG.   +10 more
europepmc   +1 more source

Connecting civic education to civil right and responsibility: a strategy for reducing high school dropout among African American students

, 2010
Charlane Starks
openalex   +1 more source

Structure–Function Decoupling of the Sensorimotor and Default Mode Networks in Black Americans With MS

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Multiple sclerosis (MS) exhibits racially disparate rates of disease progression. Black people with MS (B‐PwMS) experience a more severe disease course than non‐Hispanic White people with MS (NHW‐PwMS). Here we investigated structural and functional connectivity as well as structure–function decoupling in the ...
Emilio Cipriano, Giacomo Boffa, Maria Petracca, Marta Ponzano, Nicole Graziano, Claire Wigley, Claire Riley, Jonathan Howard, Pietro Bontempi, Sylvia Klineova, Fred Lublin, Matilde Inglese   +11 more
wiley   +1 more source

3D finite element analysis of removable partial denture with lingual bar major connector constructed with cobalt chromium, PEEK, PEKK, and BioHPP. [PDF]

BMC Oral Health
Zakaria Hashem Mostafa A, Sameh A, El Sayed El-Khamisy N.   +2 more
europepmc   +1 more source

Competition, education and assessment: connecting history with recent scholarship

, 2015
Robert H. Nelson, Phillip Dawson
openalex   +2 more sources

Validity of a Wearable Digital Insole for Assessing Gait ON and OFF in Parkinson's Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Gait impairment is a distinctive symptom of Parkinson's disease that negatively impact mobility. We assessed the validity of wearable digital insoles against a validated reference gait analysis system for measuring select gait characteristics in patients with Parkinson's disease. Methods A comparative analysis between digital insoles
Deborah A. Hall, Kimberly Kwei, Rolando J. Acosta, Bharatkumar Koyani, Erin Robertson, Pratyush Rai, Roland Barge, Emily Timm, Nicollette L. Purcell, Natasha Desai, Dhanesh Patel, Ana‐Maria Visoiu‐Knapp, Samuel Stuart, Rinol Alaj, Matthew F. Wipperman, Oren Levy, Joan A. O'Keefe   +16 more
wiley   +1 more source

Protocol to design and implement scalable wireless network system for high-throughput, automated behavioral and circuit neuroscience in mice. [PDF]

STAR Protoc
Kim CY, Parker KE, Jeong EY, Han D, Jang Y, Joo SY, Lee J, Chiangchaisakunthai C, Qazi R, Chung J, Ha S, Jeong JW, McCall JG.   +12 more
europepmc   +1 more source

Intelligently Connecting People - Facilitating Socially Appropriate communication in Mobile and Office Environments

, 2008
Maria Danninger
openalex   +1 more source

Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina, Anna Marcé‐Grau, Barbara Masotto, Marta Codina, Lamia BenJemaa, Yasmina Elaribi, Mónica Martinez‐Gallo, Roger Colobran, Angel Sanchez‐Montañez, Irene Valenzuela, Yoshiko Murakami, Alfons Macaya   +11 more
wiley   +1 more source