PROMOTING ACCESS TO AFRICAN RESEARCH

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Issue Title
 
Vol 15, No 1 (2014) Assessment of respiratory involvement in children with mucoplysaccharidosis using pulmonary function tests Abstract   PDF
MM El Falaki, MY Girgis, AA Ali, MA Elmonem, HM Ismail
 
Vol 16, No 3 (2015) Assessment of the efficacy of desmopressin in treatment of Primary Monosymptomatic Nocturnal Enuresis in Egyptian children Abstract   PDF
F ElBaz, S Zahra, M Khairy
 
Vol 18, No 3 (2017) Association analysis of polymorphisms in EGFR, HER2, ESR1 and THRA genes with coronary artery diseases Abstract   PDF
Maha Rebaї, Imen Kallel, Rania Abdelhedi, Najla kharrat, Nouha Abdemoula Bouayed, Leila Abid, Ahmed Rebaї
 
Vol 19, No 1 (2018) Association assessment of Interleukine-10 gene polymorphism and its expression status with susceptibility to coronary artery disease in Iran Abstract   PDF
Seyedeh Zahra Mousavi, Aref Salehi, Eisa Jorjani, Reza Salehi Manzari, Touraj Farazmandfar, Majid Shahbazi
 
Vol 18, No 4 (2017) Association assessment of platelet derived growth factor B gene polymorphism and its expression status with susceptibility to coronary artery disease Abstract   PDF
Shayesteh Rezayani, Touraj Farazmandfar, Majid shahbazi
 
Vol 16, No 1 (2015) Association between consanguinity and survival of marriages Abstract   PDF
M Saadat
 
Vol 19, No 1 (2018) Association between Interleukin-18 promoter polymorphisms and risk of ischemic stroke: A case-control study Abstract   PDF
Noha M. Bakr, Noha A. Hashim, Ashraf Awad, Abdallah-Almamun Sarhan
 
Vol 18, No 1 (2017) Association between interleukin-4 (IL-4), gene polymorphisms (C-589T, T+2979G, and C-33T) and migraine susceptibility in Iranian population: A case–control study Abstract   PDF
Nourollah Ramroodi, Mohammad Reza Javan, Nima Sanadgol, Mehdi Jahantigh, Tooba Nakhzari Khodakheir, Nasrin Ranjbar
 
Vol 17, No 4 (2016) Association between methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism and risk of ischemic stroke in North Indian population: A hospital based case–control study Abstract   PDF
Amit Kumar, Shubham Misra, Anjali Hazarika, Pradeep Kumar, Ram Sagar, Abhishek Pathak, Kamalesh Chakravarty, Kameshwar Prasad
 
Vol 14, No 2 (2013) Association between the polymorphisms of matrix metalloproteinases 9 and 3 genes and risk of myocardial infarction in Egyptian patients Abstract   PDF
Nadia I Sewelam, Eman R Radwan, Ashraf W Andraos, Baher E Ibrahim, Manal M Wilson
 
Vol 16, No 1 (2015) Association of β-fibrinogen promoter gene polymorphism (148C/T), hyperfibrinogenemia and ischemic stroke in young adult patients Abstract   PDF
I Imran, R Lamsudin, P Idjradinata, TH Achmad, A Maskoen, S Wibowo, H Harapan
 
Vol 17, No 1 (2016) Association of 308G/A TNF-α gene polymorphism and spontaneous preterm birth in Acehnese ethnic group, Indonesia: This polymorphism is not associated with preterm birth Abstract   PDF
Mohd Andalas, Mohammad Hakimi, Detty Siti Nurdiati, Indwiani Astuti, Imran Imran, Harapan Harapan
 
Vol 17, No 4 (2016) Association of ADAM33 gene S1 and S2 transmembrane domain polymorphisms in COPD from South-Indian population Abstract   PDF
Kolanupaka Vijaya Laxmi, Kandi Subhakar, Bodiga Vijaya Lakshmi, Ananthapur Venkateshwari, Akka Jyothy
 
Vol 19, No 2 (2018) Association of adiponectin gene (ADIPOQ) polymorphisms with measures of obesity in Nigerian young adults Abstract   PDF
Olusegun E. Ogundele, Khalid O. Adekoya, Abraham A.A. Osinubi, Awoyemi A. Awofala, Bola O. Oboh
 
Vol 16, No 3 (2015) Association of CYP3A4 and CYP3A5 polymorphisms with Iranian breast cancer patients Abstract   PDF
E Badavi, B Safavi, A Jalali, GM Shahriary, J Mohammadi-Asl, J Babaei
 
Vol 19, No 1 (2018) Association of genetic polymorphisms of PON1 and CETP with the presence of metabolic syndrome; the effects of genotypes on their serum activity and concentrations Abstract   PDF
Behdokht Fathi Dizaji, Mahdi Rivandi, Ali Javandoost, Maryam Saberi Karimian, Atena Raei, Amirhossein Sahebkar, Gordon Ferns, Majid Ghayour Mobarhan, Alireza Pasdar
 
Vol 16, No 4 (2015) Association of glutathione-S-transferase P1 (GSTP1)-313 A> G gene polymorphism and susceptibility to endometrial hyperplasia among Egyptian women Abstract   PDF
Afaf Elsaid, Wfaa Al-Kholy, Rana Ramadan, Rami Elshazli
 
Vol 15, No 4 (2014) Association of insertion–deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients Abstract   PDF
O M Hassanin, M Moustafa, T M El Masry
 
Vol 15, No 1 (2014) Association of Interleukin 27 gene polymorphism and risk of Hepatitis B viral infection in Egyptian population Abstract   PDF
YBM Ali, SA El-Masry, BA El-Akhras, SZ El-Shenawy, IH El-Sayed
 
Vol 19, No 3 (2018) Association of interleukin-6 and its -174G/C promoter polymorphism with clinical and laboratory characteristics of non hepatitis C virus rheumatoid arthritis patients Abstract   PDF
Reham Mohamed Raafat Hamed, Soliman Aref Mohamed, Reham Ali Dwedar, Yasmine Samy Elkholy, Fatema Talaat Elgengehy
 
Vol 17, No 4 (2016) Association of MTHFR polymorphisms with nsCL/P in Chinese Uyghur population Abstract   PDF
Xianrong Xu, Huiwen Pan, Lei Yu, Yu Hong
 
Vol 19, No 3 (2018) Association of nonalcoholic fatty liver disease grades with the plasma cell antigen-1 (PC-1) gene polymorphism Abstract   PDF
Ibrahim H. Borai, Yehia Mohamed Shaker, Maha Moustafa Kamal, Wafaa M. Ezzat, Esmat Ashour, Mie Afify, Weaam Gouda, Maha M. Elbrashy
 
Vol 19, No 3 (2018) Association of P2X7 gene common polymorphisms with pulmonary tuberculosis in Lur population of Iran Abstract   PDF
Ali Amiri, Toomaj Sabooteh, Seyyed Amir Yasin Ahmadi, Alireza Azargoon, Farhad Shahsavar
 
Vol 19, No 3 (2018) Association of proinflammatory cytokine IL-20 gene polymorphism with psoriasis in north Indian population Abstract   PDF
Aadil Wani, Bashir Ahmad Ganai, Tahseena Akhtar, Tarun Narang, Rajinder Kaur
 
Vol 14, No 4 (2013) Association of serum fetuin-A and fetuin-A gene polymorphism in relation to mineral and bone disorders in patients with chronic kidney disease Abstract   PDF
DA Maharem, SH Gomaa, MK El Ghandor, EI Mohamed, KA Matrawy, SS Zaytoun, HM Nomeir
 
Vol 13, No 3 (2012) Association of the UCP2 45-bp insertion/deletion polymorphism with diabetes type 2 and obesity in Saudi population Abstract   PDF
EH Jiffri
 
Vol 10, No 2 (2009) Association of the UCP2 –866G/A polymorphism with type 2 diabetes and obesity in Saudi population Abstract   PDF
MT Tayeb
 
Vol 19, No 3 (2018) Association of toll-like receptor 2 polymorphisms with susceptibility to pulmonary tuberculosis in Sudanese Abstract   PDF
H. Zaki, N. Gasmelseed, B. Abdalla, S.P. Yip
 
Vol 19, No 3 (2018) Association of variable number tandem repeats polymorphism in the IL-4 gene with end-stage renal disease in children Abstract   PDF
Eman A. Elghoroury, Fatina I. Fadel, Hebatallah Farouk, Manal F. Elshamaa, Solaf Kamel, Dina Kandil, Eman Mahmoud
 
Vol 19, No 4 (2018) Asymptomatic hemochromatosis case with HFE c.1007-47G>A, c.340+4T>C heterozygous mutations and alpha globin -3.7 kb deletion Abstract   PDF
Vesile Deniz Çelik, Betul Orhan Kiliç, Yasemin Ardıçoğlu Akışin, Fatma Ajlan Tükün, Nejat Akar
 
Vol 17, No 3 (2016) Autosomal recessive ichthyosis with limb reduction defect: A simple association and not CHILD syndrome Abstract   PDF
Rabah M Shawky, Solaf M Elsayed, Heba Amgad
 
Vol 11, No 2 (2010) Baraitser–Winter syndrome: An additional Arab patient Abstract   PDF
MMA Henedy, MJ Marafie, SJ Abulhasan
 
Vol 17, No 1 (2016) Baraitser–Winter syndrome: An additional Egyptian patient with skeletal anomalies, bilateral iris and choroid colobomas, retinal hypoplasia and hypoplastic scrotum Abstract   PDF
Rabah M. Shawky, Radwa Gamal, Shaimaa Abdelsattar Mohammad
 
Vol 13, No 2 (2012) Basic concepts of medical genetics Abstract   PDF
MSZ Salem
 
Vol 15, No 1 (2014) Basic concepts of medical genetics, formal genetics, Part 1 Abstract   PDF
MSZ Salem
 
Vol 14, No 1 (2013) Basic concepts of medical genetics, pathogenetics, Part 2 Abstract   PDF
MSZ Salem
 
Vol 14, No 3 (2013) Basic concepts of medical genetics, Pathogenetics, Part 4: Anti-mutation mechanisms of the human genome and human proteome Abstract   PDF
MSZ Salem
 
Vol 13, No 3 (2012) Basic concepts of medical genetics, pathogenetics: Part 1 Abstract   PDF
MSZ Salem
 
Vol 16, No 2 (2015) Berardinelli–Seip syndrome type 2 – An Egyptian child Abstract   PDF
RM Shawky, R Gamal, NS Seifeldin
 
Vol 16, No 2 (2015) Bicycle ergometer versus treadmill on balance and gait parameters in children with hemophilia Abstract   PDF
RA Mohamed, AEAA Sherief
 
Vol 13, No 3 (2012) Biofilm formation and presence of icaAD gene in clinical isolates of staphylococci Abstract   PDF
RA Nasr, HM AbuShady, HS Hussein
 
Vol 15, No 1 (2014) Biological evolution: Some genetic considerations Abstract   PDF
MSZ Salem
 
Vol 16, No 4 (2015) Blepharophimosis, ptosis, epicanthus inversus syndrome type 2 with red hair, lymphedema of lower limbs and kidney stones in an Egyptian patient Abstract   PDF
Rabah M Shawky, R Gamal, Neveen S Seifeldin
 
Vol 9, No 2 (2008) C syndrome in an Egyptian infant with dilated brain ventricles and heteroto pia Abstract   PDF
RM Shawky, DI Sadik
 
Vol 18, No 1 (2017) C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child Abstract   PDF
Rabah M. Shawky, Radwa Gamal
 
Vol 18, No 2 (2017) Can food addiction replace binge eating assessment in obesity clinics? Abstract   PDF
Alaa Youssef Ahmed, Amany Mohammed Sayed, Asmaa Abdelfattah Alshahat, Eman Amin Abd Elaziz
 
Vol 16, No 4 (2015) Cancer ameliorating potential of Phyllanthus amarus: In vivo and in vitro studies against Aflatoxin B1 toxicity Abstract   PDF
Sultan Ahmad, Sultana Bano, Shafaat Anwar
 
Vol 19, No 4 (2018) Cantu syndrome in an Egyptian child Abstract   PDF
Rabah M. Shawky, Radwa Gamal
 
Vol 17, No 2 (2016) Cardiological assessment of a cohort of Egyptian patients with osteogenesis imperfecta type III Abstract   PDF
Heba Salah A. ElAbd, Mohamed Moghazy
 
Vol 19, No 1 (2018) Cardiomyopathy in Vici syndrome Abstract   PDF
Rabah M. Shawky
 
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ISSN: 1110-8630
AJOL African Journals Online