Results 331 to 340 of about 362,451 (418)

Motor pathway evaluation by transcranial magnetic stimulation in Swedish horses with acquired equine polyneuropathy

open access: yesEquine Veterinary Journal, EarlyView.
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

open access: bronze, 1991
N. M. Gibbs   +3 more
openalex   +1 more source

Dysphagia in an equine referral hospital, 182 cases

open access: yesEquine Veterinary Journal, EarlyView.
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

Chronic idiopathic myopathy in Icelandic horses: A case series

open access: yesEquine Veterinary Journal, EarlyView.
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

Botulinum toxin paralysis of the orbicularis muscle [PDF]

open access: yes, 1993
Evinger, C.   +2 more
core  

Effects of HMG CoA reductase (HMGCR) deficiency on skeletal muscle development

open access: yesThe FEBS Journal, EarlyView.
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

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