Results 201 to 210 of about 2,560,284 (292)

Nurse's Compliance with Pain Assessment Documentation at Aceh General Hospital

, 2021
Eri Melfiza, Hilman Sharif, Elly Wardani
openalex   +1 more source

Interleukin‐6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini, Emanuela Martinuzzi, Sandra Dhifallah, Abderhmane Slioui, Angela Puma, Luisa Villa, Michele Cavalli, Andra Ezaru, Jérémy Garcia, Manuela Gambella, Federico Torre, Luca Jacopo Pavan, Nicolas Glaichenhaus, Sabrina Sacconi   +13 more
wiley   +1 more source

Documentation of Advance Care Planning in Early Phase Cancer Clinical Trials: An Australian Single-Centre Experience. [PDF]

Cancers (Basel)
Huang N, Descallar J, Vo S, Lee SS, Wilkinson K, Roohullah A, Cooper A, Bray V, Chua W, Ní Chróinín D, Pal A.   +10 more
europepmc   +1 more source

Patterns in Chaplain Documentation of Assessments and Interventions, a Descriptive Study

, 2015
Kevin Eugene Adams
openalex   +2 more sources

Identification of Prediabetes Discussions in Unstructured Clinical Documentation: Validation of a Natural Language Processing Algorithm (Preprint)

, 2021
Jessica L. Schwartz, Eva Tseng, Nisa M. Maruthur, Masoud Rouhizadeh   +3 more
openalex   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas, Pablo Iruzubieta, Alberto Damborenea, Laura Pérez‐Fernández, Inmaculada Azorín, Juan Carlos Jiménez García, Ana Töpf, Pilar Martí, Lorena Fores‐Toribio, María Manterola, Rosana Blanco‐Mañez, Oihane Pikatza‐Menoio, Sonia Alonso‐Martín, Volker Straub, Aitziber L. Cortajarena, Adolfo López de Munain, David De Sancho, Lorea Blázquez, Juan J. Vilchez   +18 more
wiley   +1 more source

Negligence in data recording during institutional birth: exploring health workers' perspectives on the barriers and enablers of data documentation practices. [PDF]

Arch Public Health
Taye BK, Gezie LD, Atnafu A, Mengiste SA, Kaasbøll J, Gullslett MK, Tilahun B.   +6 more
europepmc   +1 more source

The specification of documentation for anti-dumping investigation in metallurgy using ABC costing method

, 2014
Kamila Janovská, Andrea Samolejová, Zuzana Stefanovová   +2 more
openalex   +1 more source

Quantitative Assessment of Upper Limb Ataxia Using a Virtual Reality‐Based Evaluation System

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cerebellar ataxia impairs coordination and balance, reducing quality of life. Conventional clinical scales, including the Scale for the Assessment and Rating of Ataxia (SARA) and the International Cooperative Ataxia Rating Scale (ICARS), are widely used to assess ataxia but are limited by subjectivity and inter‐rater variability ...
Masayuki Sato, Takayuki Abe, Sho Aoki, Setsuki Tsukagoshi, Yasushi Yuminaka, Yoshio Ikeda   +5 more
wiley   +1 more source

Adequacy of Operative Notes for Orthopaedic Procedures: A Quality Improvement Project. [PDF]

Cureus
Jan AA, Imtiaz H, Ahmed T, Alkhatib O, Rahim AK, Kouklidis G.   +5 more
europepmc   +1 more source