Results 151 to 160 of about 13,089 (293)

Hypoxic training in thoroughbred horses

open access: yes, 2017
The aim of this study was to examine the effects of six weeks of normobaric hypoxic training when the fraction of oxygen in the inspired air (FiO2) was reduced from 0.21 to 0.15, simulating the partial pressure of oxygen at an altitude of approximately ...
Zhou, Shi   +5 more
core  

A study on the measurement of the reference range of the whole blood viscosity in Thoroughbred horses

open access: yes
This study aimed to measure the whole blood viscosity (WBV) in racehorses using a new viscometer and establish reference values, as well as to investigate the correlation between the WBV and the haematological parameters and serum chemistry.
J Lee   +6 more
core   +1 more source

Review of Congenital Myasthenic Syndrome Caused by Pathogenic Variants in GFPT1

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Glutamine:fructose‐6‐phosphate transaminase 1 (GFPT1) catalyzes the first and rate‐limiting step of the hexosamine biosynthetic pathway (HBP) to generate UDP‐GlcNAc. GFPT1 exon 9 is specifically spliced in in striated muscles, which makes a long isoform of GFPT1 (GFPT1‐L).
Kinji Ohno   +5 more
wiley   +1 more source

Auction Sale of Thoroughbred Stock

open access: yes
A piece of newspaper featuring an article for the sale of thoroughbred Jersey stock from Albert D.

core   +1 more source

Repeatability and test-retest reliability of thermal and pressure pain threshold testing in healthy thoroughbred horses. [PDF]

open access: yesFront Vet Sci
Khatib JL   +6 more
europepmc   +1 more source

Presynaptic Congenital Myasthenic Syndromes

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Presynaptic congenital myasthenic syndromes (CMS) encompass a large number of rare neurologic disorders caused by impaired release of acetylcholine (ACh) from motor nerve terminals. There are two main groups of presynaptic CMS: one in which the amount of ACh in synaptic vesicles (SV) is diminished and another in which the mechanism of synaptic
Ricardo A. Maselli
wiley   +1 more source

A Case of Distal Hereditary Motor Neuronopathy‐7 With Two Novel VWA1 Variants in Compound Heterozygosity

open access: yesNeurology and Clinical Neuroscience, EarlyView.
ABSTRACT Distal hereditary motor neuronopathy‐7 (HMNR7) is an autosomal recessive VWA1‐related disorder characterized predominantly by distal motor involvement. A 41‐year‐old man with a history of childhood orthopedic surgery for foot deformities exhibited progressive distal weakness and muscle atrophy with lower limb predominance. Electrophysiological
Toshiyuki Kakumoto   +4 more
wiley   +1 more source

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