Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Mahmoud Mohamed, Elgari"'
Publikováno v:
Cukurova Medical Journal, Vol 42, Iss 4, Pp 735-740 (2017)
Amaç: Bu çalışmada doğum şeklinin yenidoğan kordon kanı hematolojik parametreler üzerindeki etkisini değerlendirilmesi amaçlanmıştır.Gereç ve Yöntem: Bu kesitsel karşılaştırmalı çalışma, Temmuz 2014'ten Ekim 2015'e kadar Sudan
Externí odkaz:
https://doaj.org/article/ceb6cdd45c064cf3b18993098575a4b6
Autor:
Abdel Rahim Mahmoud Muddathir, Elharam Ibrahim Abdallah, Omar Falah Khabour, Ream Elzain Abdelgader, Mahmoud Mohamed Elgari
Publikováno v:
Biomolecules & Biomedicine, Vol 19, Iss 4 (2019)
The glutathione S-transferase (GST) genes encode enzymes that mediate the detoxification of xenobiotics by catalyzing the conjugation of glutathione (GSH) to xenobiotic substrates. The aim of the current study is to investigate the association betwee
Externí odkaz:
https://doaj.org/article/be430c85f3354432b2d551c239b770e2
Autor:
Nadir Ahmed Ibrahim, Fathelrahman M Hassan Gameel, Mahmoud Mohamed Elgari, Sana Eltahir Abdalla
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 9, Pp GC07-GC10 (2018)
Introduction: Thrombophilia is a multi-factorial hypercoagulability disorder. The predisposing factors may be inherited, acquired or both. Factor V Leiden prothrombin 20210G>A mutations are the most common inherited factors. Aim: This study was aimed
Externí odkaz:
https://doaj.org/article/855f9d79067f4e0f8861b5870b60a8f2
Publikováno v:
Vascular Health and Risk Management
Nadir Ahmed Ibrahim,1,2 Fathelrahman M Hassan,3 Mahmoud Mohamed Elgari,2 Sana Eltahir Abdalla4 1Department of Hematology and Immunohematology, College of Medical Laboratory Science, Sudan University of Science and Technology, Khartoum, Sudan; 2Depart
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34498186841639b9ff8bb5fceb3fe8d1
http://europepmc.org/articles/PMC6108343
http://europepmc.org/articles/PMC6108343
Autor:
Mahmoud Mohamed Elgari, Abdel Rahim Mahmoud Muddathir, Nadir Ahmed Ibrahim, Ibrahim M Ibrahim, Faris Mergheni Eltoom
Publikováno v:
Open Life Sciences, Vol 12, Iss 1, Pp 162-166 (2017)
Thrombophilia may be anticipated by single or combined hereditary defects in encoding genes factor V, Prothrombin, and MTHFR. The aim of this study was to determine the prevalence and associated risks of V Leiden (G1691A), Prothrombin (G20210A), and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6d8f8761a64e700f97b65f347b41f75
https://doaj.org/article/3c352395c7cc4c43afbcebf8ea29eec3
https://doaj.org/article/3c352395c7cc4c43afbcebf8ea29eec3
Autor:
Mahmoud Mohamed Elgari, Omar F. Khabour, Elharam Ibrahim Abdallah, Abdel Rahim Mahmoud Muddathir, Ream Elzain Abdelgader
Publikováno v:
Bosnian Journal of Basic Medical Sciences (2019)
The glutathione S-transferase (GST) genes encode enzymes that mediate the detoxification of xenobiotics by catalyzing the conjugation of glutathione (GSH) to xenobiotic substrates. The aim of the current study is to investigate the association betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8770a01ea1feb7be19539467294a2ac4
https://europepmc.org/articles/PMC6868479/
https://europepmc.org/articles/PMC6868479/
Autor:
Mahmoud Mohamed, Elgari, Omar F, Khabour, Hanim Abd Elmahmoud Hassan, Elhag, Abdel Rahim Mahmoud, Muddathir
Publikováno v:
Pakistan journal of pharmaceutical sciences. 32(2 (Supplementary))
Anemia is very common among end stage patients with chronic renal failure (CRF). In this investigation, hematological parameters were examined in patients with end stage chronic renal failure from Khartoum, Sudan. A total of 70 patients and additiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0af64dca99d359093cb67569847e1f4
https://pubmed.ncbi.nlm.nih.gov/31103969
https://pubmed.ncbi.nlm.nih.gov/31103969
Autor:
Fathelrahman M Hassan Gameel, Nadir Ahmed Ibrahim, Mahmoud Mohamed Elgari, Sana Eltahir Abdalla
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 9, Pp GC07-GC10 (2018)
Introduction: Thrombophilia is a multi-factorial hypercoagulability disorder. The predisposing factors may be inherited, acquired or both. Factor V Leiden prothrombin 20210G>A mutations are the most common inherited factors. Aim: This study was aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc5e9f580bcfa5a6d27ea6b65c56062d
Publikováno v:
Egyptian Academic Journal of Biological Sciences. C, Physiology and Molecular Biology. 5:107-112
Objective: to evaluate the clinical and diagnostic significant of lp (a) levels and other lipid and apolipoprotein profiles in diabetic patients compared with different categorization of diabetic patients. Method: Case control study determined the le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b5603ca711fe1251163df687ea6ba14
https://doi.org/10.21608/eajbsc.2013.16116
https://doi.org/10.21608/eajbsc.2013.16116
Autor:
Mahmoud Mohamed Elgari
Publikováno v:
Egyptian Academic Journal of Biological Sciences. C, Physiology and Molecular Biology. 5:1-5
Background: Various hemostatic abnormalities can occur in patients with liver disease, the severity of these abnormalities is dependent on the degree of hepatic dysfunction. Liver disease can cause both quantitative and qualitative abnormalities in c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9d902fdba39fd0bdc8965c5ac0553e1
https://doi.org/10.21608/eajbsc.2013.16102
https://doi.org/10.21608/eajbsc.2013.16102