Results 131 to 140 of about 3,559,277 (297)
Testing and Proving, Hand-in-Hand
, 2010 The motivating ideal of my lifetime’s scientific research has been that of program correctness, achieved with the aid of mathematical proof. As suggested by Turing, Floyd, and others, the proofs would be based on the decoration of a program with assertions, that would be proved true if ever they were evaluated at the point where they were written in ...
openaire +3 more sources
Beyond p‐values: Assessing clinical significance in acupuncture research
Advanced Chinese Medicine, EarlyView.Abstract In acupuncture randomized controlled trials (RCTs), the proper interpretation of results requires a thorough understanding of key statistical concepts such as p‐value, effect size, and the minimal clinically important difference (MCID). This paper explores the relationships among these metrics and their implications for assessing the clinical ...
Changzhen Gong
wiley +1 more source
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Annals of Clinical and Translational Neurology, EarlyView.Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao +34 more
wiley +1 more source
Macrophage-Derived Extracellular Vesicles: A Novel Therapeutic Alternative for Diabetic Wound
International Journal of NanomedicineShaoyan Shi, Xuehai Ou, Qian Wang, Li Zhang Department of Hand Surgery, Honghui Hospital, Xi’an Jiaotong University, Xi’an Honghui Hospital North District, Xi’an, Shaanxi, 710000, People’s Republic of ChinaCorrespondence: Li Zhang, Department of Hand ...
Shi S, Ou X, Wang Q, Zhang L
doaj
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra +17 more
wiley +1 more source
Opioid Prescribing Patterns and Characteristics of Hand Injury Presentations to the Emergency Department of a Surgical Referral Centre in Western Sydney. [PDF]
Emerg Med AustralasStocca M, Nguyen K, Chandru P.
europepmc +1 more source
Precision‐Optimised Post‐Stroke Prognoses
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background Current medicine cannot confidently predict who will recover from post‐stroke impairments. Researchers have sought to bridge this gap by treating the post‐stroke prognostic problem as a machine learning problem, reporting prediction error metrics across samples of patients whose outcomes are known.
Thomas M. H. Hope +4 more
wiley +1 more source