Congenital syndromes of pain and painlessness
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| Other Authors: | |
|---|---|
| Format: | Electronic Video |
| Language: | English |
| Published: |
London :
Henry Stewart Talks,
2014.
|
| Series: | Henry Stewart talks. Biomedical & life sciences collection. Molecular genetics of human disease.
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| Subjects: | |
| Online Access: | https://hstalks.com/bs/2893/ Series |
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| 028 | 5 | 0 | |a 3660 |b Henry Stewart Talks |
| 035 | |a (UkLoHST)2893 | ||
| 040 | |a UkLoHST |b eng |c UkLoHST | ||
| 100 | 1 | |a Woods, Geoff, |u (University of Cambridge, UK) |4 spk |9 103163 | |
| 245 | 1 | 0 | |a Congenital syndromes of pain and painlessness |h [electronic resource] / |c Geoff Woods. |
| 260 | |a London : |b Henry Stewart Talks, |c 2014. | ||
| 300 | |a 1 online resource (1 streaming video file (57 min.) : |b color, sound). | ||
| 490 | 1 | |a Molecular genetics of human disease, |x 2056-452X | |
| 500 | |a Animated audio-visual presentation with synchronized narration. | ||
| 500 | |a Title from title frames. | ||
| 505 | 0 | |a Contents: What is pain? -- How much pain is someone suffering? -- What is the use of pain? -- Pain pathways -- Types of pain (Nociceptive, Inflammatory, Neuropathic, mixed) -- Primary erythromelalgia -- Mutations in SCN9A cause erythromelalgia -- Voltage-gated ion channels -- Paroxysmal extreme pain disorder (familial rectal pain) -- Mutations in SCN9A cause PEPD -- Congenital insensitivity to pain -- SCN9A gene map -- Electrical activity of wild type versus mutant constructs -- Low-copy number vector = pcDNA3JC -- Exon 6 splice variants -- Neuropathies HSANs -- Rita Levi Montalcini -- TRKA signalling -- Hereditary autonomic and sensory neuropathy type 4 (HSAN4) -- HSAN5 -- NGFB -- Familial dysautonomia -- Treatment of pain -- Mendelian disorders of pain. | |
| 506 | |a Access restricted to subscribers. | ||
| 538 | |a Mode of access: World Wide Web. | ||
| 650 | 0 | |a Congenital insensitivity to pain. |9 103164 | |
| 650 | 0 | |a Genetic disorders. |9 103165 | |
| 650 | 0 | |a Pain. |9 103166 | |
| 650 | 2 | |a Dysautonomia, Familial. |9 103167 | |
| 650 | 2 | |a Erythromelalgia. |9 103168 | |
| 650 | 2 | |a Hereditary Sensory and Autonomic Neuropathies. |9 103169 | |
| 650 | 2 | |a Pain Insensitivity, Congenital. |9 103170 | |
| 650 | 2 | |a Pain. |9 103171 | |
| 650 | 2 | |a Paroxysmal Extreme Pain Disorder. |9 103172 | |
| 830 | 0 | |a Henry Stewart talks. |p Biomedical & life sciences collection. |p Molecular genetics of human disease. |9 103173 | |
| 856 | 4 | 0 | |u https://hstalks.com/bs/2893/ |
| 856 | 4 | 2 | |u https://hstalks.com/bs/p/810/ |3 Series |
| 999 | |c 215019 |d 215018 | ||
Understanding pain an exploring the perception of pain /