Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Hatem A Aman"'
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0249284 (2021)
Mental illness is prevalent among hemodialysis (HD) patients. Given that the dopaminergic and serotonergic pathways are involved in the etiology of psychiatric disease, this study evaluated the genetic association of dopamine D4 receptor (DRD4) and s
Externí odkaz:
https://doaj.org/article/ae91b68aa7ab42f39f63ef9e4088517a
Publikováno v:
PLoS ONE, Vol 15, Iss 6, p e0235001 (2020)
Effective adoption of genetics in clinical practice requires the support of and interaction between the different partners of healthcare system; healthcare professionals (HCPs) and patients. The study aimed to assess and compare the knowledge, factor
Externí odkaz:
https://doaj.org/article/9d2771d5c8b4459c8c6e05340cbd9aa4
Autor:
Laith N. AL-Eitan, Mansour A. Alghamdi, Ayah Y Almasri, Nasr Alrabadi, Hatem A Aman, Rame Khasawneh, Adan H Alnaamneh
Publikováno v:
International Journal of Medical Sciences. 18:826-834
Cardiovascular diseases are among the leading causes of death worldwide. Many of those diseases require treatment with warfarin, an anticoagulant that has a large high inter and intra-variability in the required doses. The aim of this study is to fin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0eec1bdfbd69bb0d8192e424ec4b4c8
https://doi.org/10.7150/ijms.51546
https://doi.org/10.7150/ijms.51546
Autor:
Hatem A Aman, Ayah Y Almasri, Laith N. AL-Eitan, Mansour A. Alghamdi, Barakat Z Elsaqa, Rame Khasawneh
Publikováno v:
Pharmacogenomics and Personalized Medicine. 13:619-632
Background Cardiovascular disease is one of the most common causes of morbidity and mortality worldwide. Several cardiovascular diseases require therapy with warfarin, an anticoagulant with large interindividual variability resulting in dosing diffic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2776c2b9921a1b197d76741766dcac7e
https://doi.org/10.2147/pgpm.s274246
https://doi.org/10.2147/pgpm.s274246
Publikováno v:
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 13:1825-1834
Objective To investigate the genotypic and allelic association of Src homology 2 B adapter protein 1 (SH2B1) gene polymorphisms with type 2 diabetes mellitus (T2DM) in Jordanian patients. Patients and Methods Three hundred patients were screened, but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d624ed87cf6dbd75bc7816a9570b323e
https://doi.org/10.2147/dmso.s245843
https://doi.org/10.2147/dmso.s245843
Autor:
Rami Alkhatib, Laith N. AL-Eitan, Hanan A Aljamal, Mansour A. Alghamdi, Rame Khasawneh, Ahmad Al-Assi, Hatem A Aman, Ayah Y Almasri
Publikováno v:
International Journal of General Medicine.
Mansour A Alghamdi,1,2 Laith AL-Eitan,3 Rami Alkhatib,3 Ahmad Al-Assi,4 Ayah Almasri,3 Hanan Aljamal,3 Hatem Aman,3 Rame Khasawneh5 1Department of Anatomy, College of Medicine, King Khalid University, Abha, 61421, Saudi Arabia; 2Genomics and Personal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aee9b4a137df613c013ffea2f74fd212
https://www.dovepress.com/variants-in-cdhr3-cacnac1-and-lta-genes-predisposing-sensitivity-and-r-peer-reviewed-article-IJGM
https://www.dovepress.com/variants-in-cdhr3-cacnac1-and-lta-genes-predisposing-sensitivity-and-r-peer-reviewed-article-IJGM
Publikováno v:
Archives of oral biology. 121
The aim of this study is to genotype thirteen Single Nucleotide Polymorphisms (SNPs) within the paired box gene 9 (PAX9) in 36 Jordanian Arab families with peg-shaped teeth, and also to investigate the association between the PAX9 gene and peg-shaped
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e9bdcf39d5f10f457ba09d0370f2161
https://pubmed.ncbi.nlm.nih.gov/33197803
https://pubmed.ncbi.nlm.nih.gov/33197803
Autor:
Laith N, Al-Eitan, Ayah Y, Almasri, Adan H, Alnaamneh, Hatem A, Aman, Nasr N, Alrabadi, Rame H, Khasawneh, Mansour A, Alghamdi
Publikováno v:
International Journal of Medical Sciences
Cardiovascular diseases are among the leading causes of death worldwide. Many of those diseases require treatment with warfarin, an anticoagulant that has a large high inter and intra-variability in the required doses. The aim of this study is to fin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::502ec838ba48e2bc7ef0fc970c764c02
https://pubmed.ncbi.nlm.nih.gov/33437219
https://pubmed.ncbi.nlm.nih.gov/33437219
Autor:
Laith N, Al-Eitan, Barakat Z, Elsaqa, Ayah Y, Almasri, Hatem A, Aman, Rame H, Khasawneh, Mansour A, Alghamdi
Publikováno v:
Pharmacogenomics and Personalized Medicine
Background Cardiovascular disease is one of the most common causes of morbidity and mortality worldwide. Several cardiovascular diseases require therapy with warfarin, an anticoagulant with large interindividual variability resulting in dosing diffic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::336d15b483619e75691bdfdaa8da35b1
https://pubmed.ncbi.nlm.nih.gov/33235484
https://pubmed.ncbi.nlm.nih.gov/33235484
Publikováno v:
Asian Pacific Journal of Cancer Prevention : APJCP
Objective In Jordan, breast cancer (BC) affects a substantial proportion of Jordanian women, highlighting the need for studies to be carried out regarding the genetic component of the disease. The aim of the present study was to investigate the inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc0b74c555395f6c4e3912c70ebc76ae
https://pubmed.ncbi.nlm.nih.gov/33112566
https://pubmed.ncbi.nlm.nih.gov/33112566