no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
ACE DD genotype associated with the female Chronic Kidney Disease patients of Tamilnadu population
|
Nagamani, Selvaraman |
|
2015 |
16 |
1 |
p. 29-33 5 p. |
article |
2 |
Ankaferd Blood Stopper induces apoptosis and regulates PAR1 and EPCR expression in human leukemia cells
|
Mumcuoglu, Mine |
|
2015 |
16 |
1 |
p. 19-27 9 p. |
article |
3 |
Apelin rs2235306 polymorphism is not related to metabolic syndrome in Egyptian women
|
Mehanna, Eman T. |
|
2015 |
16 |
1 |
p. 35-40 6 p. |
article |
4 |
Association between consanguinity and survival of marriages
|
Saadat, Mostafa |
|
2015 |
16 |
1 |
p. 67-70 4 p. |
article |
5 |
Association of β-fibrinogen promoter gene polymorphism (−148C/T), hyperfibrinogenemia and ischemic stroke in young adult patients
|
Imran, Imran |
|
2015 |
16 |
1 |
p. 11-17 7 p. |
article |
6 |
Cancer: Some genetic considerations
|
Salem, Mohammad Saad Zaghloul |
|
2015 |
16 |
1 |
p. 1-10 10 p. |
article |
7 |
Cytokeratin 18 as a non invasive marker in diagnosis of NASH and its usefulness in correlation with disease severity in Egyptian patients
|
Maher, Mohsen M. |
|
2015 |
16 |
1 |
p. 41-46 6 p. |
article |
8 |
Editorial Board
|
|
|
2015 |
16 |
1 |
p. iii-iv nvt p. |
article |
9 |
Effect of a new physical therapy concept on dynamic balance in children with spastic diplegic cerebral palsy
|
Emara, Hatem Abdel Mohsen Abdel Hamid |
|
2015 |
16 |
1 |
p. 77-83 7 p. |
article |
10 |
Effect of hand-arm bimanual intensive therapy on fine-motor performance in children with hemiplegic cerebral palsy
|
Abd El Wahab, Manal |
|
2015 |
16 |
1 |
p. 55-59 5 p. |
article |
11 |
Fetal gender determination through Y-STR analysis of maternal plasma during the third trimester of pregnancy
|
Aal-Hamdan, Hanaa M.H. |
|
2015 |
16 |
1 |
p. 47-53 7 p. |
article |
12 |
Frequency distribution of ABO and Rh (D) blood group alleles in Silte Zone, Ethiopia
|
Tesfaye, Kassahun |
|
2015 |
16 |
1 |
p. 71-76 6 p. |
article |
13 |
Hardy–Weinberg disequilibrium and association study of insertion/deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients
|
Hassanin, Omayma M. |
|
2015 |
16 |
1 |
p. 85-86 2 p. |
article |
14 |
Primary ciliary dyskinesia: Kartagener syndrome in a family with a novel DNAH5 gene mutation and variable phenotypes
|
Marafie, Makia J. |
|
2015 |
16 |
1 |
p. 95-99 5 p. |
article |
15 |
Some aspects of genetics and pharmacogenetics understanding by pharmacy students in Ukraine
|
Filiptsova, O.V. |
|
2015 |
16 |
1 |
p. 61-66 6 p. |
article |
16 |
Subclinical hypothyroidism in children with Down syndrome: To treat or not to treat???
|
El Kholy, Mohamed |
|
2015 |
16 |
1 |
p. 87-88 2 p. |
article |
17 |
Trichorhinophalangeal syndrome II, expanding the clinical spectrum
|
Shawky, Rabah M. |
|
2015 |
16 |
1 |
p. 89-94 6 p. |
article |