Medical Functioning and Circadian Dysrhythmia
نویسندگان
چکیده
منابع مشابه
Sleep, circadian dysrhythmia, obesity and diabetes
Synchrony of biological processes with environmental cues developed over millennia to match growth, reproduction and senescence. This entails a complex interplay of genetic, metabolic, chemical, light, hormonal and hedonistic factors across life forms. Sleep is one of the most prominent rhythms where such a match is established. Over the past 100 years or so, it has been possible to disturb the...
متن کاملCircadian rhythm. Dysrhythmia in the suprachiasmatic nucleus inhibits memory processing.
Chronic circadian dysfunction impairs declarative memory in humans but has little effect in common rodent models of arrhythmia caused by clock gene knockouts or surgical ablation of the suprachiasmatic nucleus (SCN). An important problem overlooked in these translational models is that human dysrhythmia occurs while SCN circuitry is genetically and neurologically intact. Siberian hamsters (Phod...
متن کاملDysrhythmia and oral surgery.
Two hundred and three male patients undergoing oral surgery were monitored for abnormalities of cardiac rhythm. Eight per cent of a smaller number of patients (seventy-six) developed ectopic rhythms during induction of anaesthesia and in half of all patients nodal rhythm was seen. Twenty-three per cent developed ectopic rhythms in response to surgery. In three per cent of patients these were of...
متن کاملThalamocortical dysrhythmia and chronic pain
The paper byWalton et al. [13] in this issue of Pain brings a new perspective to the problem of central pain, in this case complex regional pain syndrome without peripheral nerve injury (CRPSI). It is a perspective that may have escaped the notice of many pain scientists and sensory physiologists. Walton et al. [13] using magnetoencephalography (MEG) compared brain activity in sufferers from ty...
متن کاملAlternating Hemiplegia and Cardiac Dysrhythmia
Investigators at the National Hospital for Neurology and Neurosurgery, Queen Square, London, and multiple centers in the UK, Europe, US, Melbourne, Australia, and Canada, analyzed ECG recordings of 52 patients with alternating hemiplegia from 9 countries; all had whole-exome, whole-genome, or direct Sanger sequencing of ATP1A3; 47 had a confirmed missense mutation in ATP1A3.
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ژورنال
عنوان ژورنال: Military Medicine
سال: 1987
ISSN: 0026-4075,1930-613X
DOI: 10.1093/milmed/152.6.308