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David Burke

Researcher at Royal Prince Alfred Hospital

Publications -  408
Citations -  26730

David Burke is an academic researcher from Royal Prince Alfred Hospital. The author has contributed to research in topics: Reflex & Muscle spindle. The author has an hindex of 89, co-authored 395 publications receiving 24952 citations. Previous affiliations of David Burke include Elsevier & Ege University.

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Book ChapterDOI

The Human Muscle Spindle and its Fusimotor Control

TL;DR: It is now 25 years since Hagbarth and Vallbo (1968) described the technique of microneurography, with the first direct recordings of the activity of muscle afferents in human subjects, to take stock of what has been learnt about fusimotor control of human muscle spindles since then.
Journal ArticleDOI

Segmental motoneuronal dysfunction is a feature of amyotrophic lateral sclerosis.

TL;DR: Changes in the slope ratio (Hθ/Mθ) in ALS suggested that alterations in peripheral motor nerve excitability following UMN damage may affect the recorded H-reflex, and further insight is provided into the pathophysiology of ALS.
Journal ArticleDOI

Larval Environment Alters Amphibian Immune Defenses Differentially across Life Stages and Populations

TL;DR: The work suggests that the susceptibility of amphibians to emerging diseases could be related to variability in the larval environment and calls for research into the relative influence of potentially less benign anthropogenic environmental changes on innate immune defense traits.
Journal ArticleDOI

Component of muscle spindle discharge related to arterial pulse

TL;DR: The arterial pulse can be significant contributor to the variability of muscle spindle discharge and the pulsatile effects seen in the responses of single afferents are unlikely to be eliminated in the summed activity forming the population response.
Journal ArticleDOI

Abnormalities of axonal excitability are not generalized in early multifocal motor neuropathy.

TL;DR: This study provides no evidence for a generalized subclinical abnormality in MMN, at least when disease duration is less than 6 years, and indices of axonal excitability were similar to those in controls.