Results 281 to 290 of about 13,221,289 (346)

T-Rx: A toolbox for reproducible processing of prescriptions (Rx) from electronic health records

Lo CWH, Handley D, Pain O, Kamp M, Gillett AC, Iveson MH, Fabbri C, Young KG, AMBER Research Team, Lewis CM.   +9 more
europepmc   +1 more source

End user experiences of an electronic health records platform in a tertiary hospital system in Kenya. [PDF]

PLoS One
Shrestha A, Shah J, Khakhar Z, Ruiz A, Talib Z, Ali SK.   +5 more
europepmc   +1 more source

Record Results Analysis Electrocardiogram (ECG) at Pangandaran Health Center

, 2019
Dedi Supriadi, Rudi Kurniawan, Hilman Firman Esa, Jajuk Kusumawaty, Atun Farihatun, Rosmiati Rosmiati   +5 more
openalex   +1 more source

Discovery and Targeted Proteomic Studies Reveal Striatal Markers Validated for Huntington's Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Clinical trials for Huntington's disease (HD) enrolling persons before clinical motor diagnosis (CMD) lack validated biomarkers. This study aimed to conduct an unbiased discovery analysis and a targeted examination of proteomic biomarkers scrutinized by clinical validation. Methods Cerebrospinal fluid was obtained from PREDICT‐HD and
Daniel Chelsky, Cara Joyce, H. Jeremy Bockholt, Paul A. Rudnick, William H. Adams, Fiona McAllister, Justin W. Smock, Michael A. Newton, Jane S. Paulsen   +8 more
wiley   +1 more source

Integrating Artificial Intelligence, Electronic Health Records, and Wearables for Predictive, Patient-Centered Decision Support in Healthcare. [PDF]

Healthcare (Basel)
Fernandes Prabhu D, Gurupur V, Stone A, Trader E.   +3 more
europepmc   +1 more source

Effectiveness and Safety of Nusinersen and Risdiplam in Spinal Muscular Atrophy: A Systematic Review

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring comprehensive medical and supportive care.
Amin Mehrabian, Peter Auguste, Amy Grove, Anna Brown, Janette Parr, Mubarak Patel, Furqan Butt, Jeremiah Donoghue, Mehdi Yousefi, Jo Parsons   +9 more
wiley   +1 more source

Comorbidity analysis and clustering of endometriosis patients using electronic health records. [PDF]

Cell Rep Med
Khan U, Oskotsky TT, Yilmaz BD, Roger J, Gjoni K, Irwin JC, Opoku-Anane J, Elhadad N, Giudice LC, Sirota M.   +9 more
europepmc   +1 more source

Evaluation of the Efficacy and Safety of Satralizumab in a Pregnant NMOSD Patient With AQP4/MOG‐IgG Dual Seropositive: A Case Report

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Neuromyelitis Optica Spectrum Disorder (NMOSD) is a chronic autoimmune neuroinflammatory disease, typically characterized by antibodies against aquaporin 4 (AQP4‐IgG) or myelin oligodendrocyte glycoprotein (MOG‐IgG). Simultaneous seropositivity for both antibodies in a single patient is exceedingly rare.
Yeting Luo, Shuhua Xie, Xianghong Liu
wiley   +1 more source