000 | 01942ngm a2200337 a 4500 | ||
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001 | HST2009_1_2 | ||
003 | UkLoHST | ||
006 | m c | ||
007 | cr|cna|||a|||| | ||
007 | vz|czazum | ||
008 | 080121s2008 enk|||||||||||s|||v|eng d | ||
028 | 5 | 0 |
_a2009 _bHenry Stewart Talks |
035 | _a(UkLoHST)1059 | ||
035 | _a(UkLU-K)000947317 | ||
040 |
_aUkLU-K _beng _cUkLU-K |
||
100 | 1 |
_aHumphries, Steve E. _4spk |
|
245 | 1 | 0 |
_aFamilial hyperchlolesterolaemia _h[electronic resource] : _ba monogenic cause of early CHD / _cSteve Humphries. |
260 |
_aLondon : _bHenry Stewart Talks, _c2008. |
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300 |
_a1 online resource (1 streaming video file (50 min.) : _bcolor, sound). |
||
490 | 1 |
_aGenetics of cardiovascular disease : genetic interactions in a multifactorial disease, _x2056-452X |
|
500 | _aAnimated audio-visual presentation with synchronized narration. | ||
500 | _aTitle from title frames. | ||
505 | 0 | _aContents: Clinical diagnostic criteria -- Prevalence in UK -- Effects of statins on cholesterol and CHD risk lowering -- The 3 genes where mutations cause FH (LDLR, APOB, PCSK9) -- Clinical Genetics Diagnostic service for FH and examples in families -- Cascade testing for FH patients using LDL cholesterol levels -- The Overlap problem -- The Simon Broome FH register project and the high risk of early CHD in those with an LDLR and PCSK9 mutation -- The LDLR mutation database -- Ethical issues about genetic testing for FH -- Clinical questions in the management of FH -- FH testing and insurance. | |
506 | _aAccess restricted to subscribers. | ||
538 | _aMode of access: World Wide Web. | ||
650 | 2 |
_aCardiovascular Diseases _xgenetics. |
|
650 | 2 |
_aHypercholesterolemia _xgenetics. |
|
830 | 0 |
_aHenry Stewart talks. _pBiomedical & life sciences collection. _pGenetics of cardiovascular disease. |
|
856 | 4 | 0 | _uhttps://hstalks.com/bs/1059/ |
856 | 4 | 2 |
_uhttps://hstalks.com/bs/p/379/ _3Series |
999 |
_c78450 _d78450 |