nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Absence of coronary artery calcium does not exclude coronary artery disease in FH patients
|
Israni, A. |
|
|
43 |
S |
p. S7 |
artikel |
2 |
APOE gene testing in FH referrals – the story so far
|
Duff-Farrier, C. |
|
|
43 |
S |
p. S2 |
artikel |
3 |
Corneal confocal microscopy detects Small nerve fibre damage in patients with heterozygous familial hypercholesterolemia which ameliorated after treatment with PCSK9 inhibitor therapy
|
Ferdousi, Maryam |
|
|
43 |
S |
p. S2-S3 |
artikel |
4 |
Does socioeconomic status have an effect on the treatment and outcomes of individuals with familial hypercholesterolaemia (FH)? : a cohort study of individuals with FH in UK primary care
|
Iyen, B. |
|
|
43 |
S |
p. S4 |
artikel |
5 |
Frequency of Lipoprotein (a) Single Nucleotide Polymorphisms in patients undergoing Familial Hypercholesterolaemia genetic testing
|
Reay, D. |
|
|
43 |
S |
p. S3 |
artikel |
6 |
Genomic testing in patients with suspected Familial Chylomicronaemia Syndrome (FCS) and evaluation of the FCS clinical scoring tool
|
Evans, J.C. |
|
|
43 |
S |
p. S3 |
artikel |
7 |
Identification of FH-causing variants in patients with clinical familial hypercholesterolaemia recruited into the 100,000 genome project: preliminary analysis
|
Rimbert, A. |
|
|
43 |
S |
p. S4 |
artikel |
8 |
Identifying familial hypercholesterolemia (FH) in Hampshire general medical practices: a systematic approach – Interim Results
|
Haigh, J. |
|
|
43 |
S |
p. S4-S5 |
artikel |
9 |
Inpatient management of severe hypertriglyceridaemia at a tertiary centre
|
Yang, W. |
|
|
43 |
S |
p. S9 |
artikel |
10 |
LIPOPROTEIN (a) LEVELS IN MONOGENIC VERSUS POLYGENIC HYPERCHOLESTEROLEMIA
|
Jain, A. |
|
|
43 |
S |
p. S7-S8 |
artikel |
11 |
Prospective evaluation of the FAMCAT tool to identify Familial Hypercholesterolaemia (FH) in primary care
|
Kirubakaran, Arushan |
|
|
43 |
S |
p. S8 |
artikel |
12 |
Reduction in cardiovascular disease morbidity of men and women with familial hypercholesterolaemia (FH) associated with availability of high intensity statins: A cohort study using data from the UK Simon Broome Register linked with secondary care records
|
Iyen, B. |
|
|
43 |
S |
p. S5 |
artikel |
13 |
Severe dyslipidaemia associated with dual heterozygosity for 2 genes causing hyperalpHalipoproteinaemia
|
Kim, Eun Ji |
|
|
43 |
S |
p. S8 |
artikel |
14 |
Small nerve fibre damage in patients with severe hypertriglyceridaemia
|
D’Onofrio, Luca |
|
|
43 |
S |
p. S3-S4 |
artikel |
15 |
The diagnostic yield for FH proband genetic testing is lower in postmenopausal women when fixed LDL-C decision thresholds are used
|
Luvai, A. |
|
|
43 |
S |
p. S8-S9 |
artikel |
16 |
The West Midland Familial Hypercholesterolaemia (FH) screening programme: Evaluating the utility of the 12 SNP polygenic risk score (PRS) across ethnic groupings
|
George, E. |
|
|
43 |
S |
p. S5-S6 |
artikel |
17 |
Title Page
|
|
|
|
43 |
S |
p. 1 |
artikel |