| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormal maternal biomarkers of homocysteine and methionine metabolism and the risk of congenital heart defects
|
Shawky, Rabah M.
|
|
2018
|
19 |
1 |
p. 7-12
|
artikel
|
| 2 |
An association between apo-A4 gene polymorphism (Thr347Ser and Gln360His) and coronary artery disease in northern India
|
Kumar, Pramod
|
|
2018
|
19 |
1 |
p. 23-29
|
artikel
|
| 3 |
Association assessment of Interleukine-10 gene polymorphism and its expression status with susceptibility to coronary artery disease in Iran
|
Zahra Mousavi, Seyedeh
|
|
2018
|
19 |
1 |
p. 31-35
|
artikel
|
| 4 |
Association between Interleukin-18 promoter polymorphisms and risk of ischemic stroke: A case-control study
|
Bakr, Noha M.
|
|
2018
|
19 |
1 |
p. 13-18
|
artikel
|
| 5 |
Association of genetic polymorphisms of PON1 and CETP with the presence of metabolic syndrome; the effects of genotypes on their serum activity and concentrations
|
Dizaji, Behdokht Fathi
|
|
2018
|
19 |
1 |
p. 43-48
|
artikel
|
| 6 |
Cardiomyopathy in Vici syndrome
|
Elsayed, Solaf M.
|
|
2018
|
19 |
1 |
p. 49-50
|
artikel
|
| 7 |
Common variant of 5,10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian population
|
Attar, Marzieh
|
|
2018
|
19 |
1 |
p. 1-5
|
artikel
|
| 8 |
Prevalence of congenital heart defects among 54 Egyptian children with Maple syrup urine disease
|
Kotby, Alyaa A.
|
|
2018
|
19 |
1 |
p. 37-41
|
artikel
|
| 9 |
Progress in genetics of coronary artery disease
|
Gamal, Radwa
|
|
2018
|
19 |
1 |
p. 51-52
|
artikel
|
| 10 |
The relation of thrombomodulin G33A and C1418T gene polymorphisms to the risk of acute myocardial infarction in Egyptians
|
Alkhiary, Wael
|
|
2018
|
19 |
1 |
p. 19-22
|
artikel
|
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