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                             17 results found
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
                             17 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands