Results 331 to 340 of about 362,451 (418)
Abstract Background Acquired equine polyneuropathy in Nordic horses (AEP) is the most prevalent equine polyneuropathy in Norway, Sweden, and Finland and is characterised by pelvic limb knuckling due to metatarsophalangeal extension dysfunction.
Anna May+6 more
wiley +1 more source
The Onset and Duration of Neuromuscular Blockade Using Combinations of Atracurium and Vecuronium
N. M. Gibbs+3 more
openalex +1 more source
Dysphagia in an equine referral hospital, 182 cases
Abstract Background Dysphagia describes a clinical sign of pathologies of the oral cavity, pharynx, and oesophagus that carries potentially serious consequences for horses. Given the diversity of differential diagnoses that may cause dysphagia, an understanding of the prevalence of dysphagia in hospitalised patients, the distribution of aetiologies and
Kevin M. Connolly, Krista Estell
wiley +1 more source
The effect of glycopyrrolate vs. atropine in combination with neostigmine on cardiovascular system for reversal of residual neuromuscular blockade in the elderly: a randomized controlled trial. [PDF]
Wang Y, Ren L, Li Y, Zhou Y, Yang J.
europepmc +1 more source
Chronic idiopathic myopathy in Icelandic horses: A case series
Abstract Background Exertional myopathies are recognised as a cause of poor performance in equines. In Icelandic horses presenting reduced performance and/or multi‐limb lameness, no specific myopathy has been identified. Objectives To characterise the clinical presentation and histopathological findings in muscle biopsy samples from Icelandic horses ...
Sanni Hansen+6 more
wiley +1 more source
Quantitative Analysis of the Effect of Neuromuscular Blockade on Motor-Evoked Potentials in Patients Undergoing Brain Tumor Removal Surgery: A Prospective, Single-Arm, Open-Label Observational Study. [PDF]
Chae D+8 more
europepmc +1 more source
Effects of HMG CoA reductase (HMGCR) deficiency on skeletal muscle development
Three skeletal muscle diseases are linked to HMGCR, a key enzyme in cholesterol synthesis. These diseases include a muscular dystrophy associated with pathogenic variants in the HMGCR gene, statin‐associated myopathy, and autoimmune anti‐HMGCR myopathy.
Mekala Gunasekaran+20 more
wiley +1 more source