 | | Hypertension & Genetics |
|  | | Where are the genes for hypertension? |
|
 | | Methods for detecting genes for hypertension |
|  | | Is hypertension ‘just’ the skewed end of the normal BP distribution? |
|
 | | Principal pathways and disorders altering sodium reabsorption in the nephron |
|  | | Principal pathways and disorders altering sodium reabsorption in the nephron |
|
 | | Principal pathways and disorders altering sodium reabsorption in the nephron |
|  | | Principal pathways and disorders altering sodium reabsorption in the nephron |
|
 | | Liddle’s syndrome: how genetic truncation causes gain of function |
|  | | Apparent Mineralocorticoid Excess |
|
 | | Low K+, low renin, low aldosterone = ? liquorice |
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|  | | Novel mutations for Gordon’s syndrome identified by whole exome sequencing |
|
 | | From monogenic to complex: the numbers game |
|  | | From monogenic to complex: the numbers game |
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|  | | ‘Manhattan plot’ showing genetic complexity of hypertension |
|
 | | Relative Risk from GWAS loci |
|  | | Relative Risk from GWAS loci |
|
 | | Breadth of loci of genetic association |
|  | | Breadth of loci of genetic association |
|
 | | Somatic mutations of the adrenal: the commonest cause of hypertension |
|  | | Microarray, qPCR and KCNJ5 sequencing shows different profiles for zona glomerulosa (ZG) and fasciculata (ZF) tumors |
|
 | | Conn’s Adenoma |
|  | | Conn’s Adenoma |
|
 | | Are KCNJ5 mutations common and does their finding influence clinical management? |
|  | | KCNJ5 genotype:phenotype I |
|
 | | KCNJ5 genotype:phenotype II |
|  | | KCNJ5 genotype:phenotype II |
|
 | | KCNJ5 genotype:phenotype II |
|  | | Early diagnosis of APA by 11C-metomidate PET CT |
|
 | | Early diagnosis of APA by PET CT |
|  | | Early diagnosis of APA by PET CT |
|
 | | Summary |
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02. Brown [Compatibiliteitsmodus] (PDF 3,8MB)
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