Results 261 to 270 of about 6,083,333 (340)

The Impact of Tilburg Frailty on Poststroke Fatigue in First‐Ever Stroke Patients: A Cross‐Sectional Study With Unified Measurement Tools and Improved Statistics

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Poststroke fatigue (PSF) and frailty share substantial overlap in their manifestations, yet previous research has yielded conflicting results due to the use of heterogeneous frailty assessment tools. Objective To evaluate the independent impact of frailty on PSF using a unified measurement system (Tilburg Frailty Indicator, TFI ...
Chuan‐Bang Chen, Xiao‐Xue Wang, Shao‐Rui Bao, Sui‐Li Lin, Mei‐Chun Shu, Xi‐Xi Ye, Wen‐Jie Cong   +6 more
wiley   +1 more source

Integration of pharmacists into primary care teams for high-risk Medicare patients. [PDF]

Proc (Bayl Univ Med Cent)
Winter FD.
europepmc   +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

Correction to Supporting Information for Han et al., CASKIN2 mediates PTPσ-orchestrated transsynaptic mechanisms at excitatory synapses. [PDF]

Proc Natl Acad Sci U S A
europepmc   +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

Bridging the Gap: Identifying and Overcoming Barriers to CAR-T Access Through Streamlined and Standardized Pathways. [PDF]

Mayo Clin Proc Innov Qual Outcomes
Uttam Chandani K, Khera N.
europepmc   +1 more source

Blucher Material Science Proceedings

openalex   +2 more sources

2014 SICPRE Proceedings: Meeting Proceedings.

Plastic and reconstructive surgery. Global open, 2015
openaire   +1 more source

ON THE ISSUE OF LEGISLATIVE ENSHRINEMENT OF THE POSSIBILITY OF USING EVIDENCE IN ELECTRONIC FORM AS A PROMISING DIRECTION FOR DIGITALIZATION OF PROCEEDINGS IN CASES OF ADMINISTRATIVE OFFENSES

A. V. Karpushkin
openalex   +1 more source

Correction for He et al., GATA2 facilitates steroid receptor coactivator recruitment to the androgen receptor complex. [PDF]

Proc Natl Acad Sci U S A
europepmc   +1 more source