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Issue Title
Vol 9, No 1 (2008) Indicators of Apoptosis in Duchenne Muscular Dystrophy Patients Abstract   PDF
E Abdel-Salam, L Mansour, I Abdel-Meguid, S Korraa
Vol 17, No 2 (2016) Inducible protective processes in animal systems XIV: Cytogenetic adaptive response induced by EMS or MMS in bone marrow cells of diabetic mouse Abstract   PDF
BB Dada Khalandar, V Vasudev
Vol 14, No 3 (2013) Insight into Nek2A activity regulation and its pharmacological prospects Abstract   PDF
A Kumar, V Rajendran, R Sethumadhavan, R Purohit
Vol 15, No 3 (2014) Insulin resistance in obese pre-pubertal children: Relation to body composition Abstract   PDF
H Elsedfy, N H Amr, O Hussein, M El Kholy
Vol 16, No 2 (2015) Integrated effect of treadmill training combined with dynamic ankle foot orthosis on balance in children with hemiplegic cerebral palsy Abstract   PDF
AEAA Sherief, AAA Gazya, MAA El Gafaar
Vol 15, No 1 (2014) Interleukin 10 gene promoter polymorphism and risk of diffuse large B cell lymphoma (DLBCL) Abstract   PDF
RM Talaat, AM Abdel-Aziz, EA El-Maadawy, N Abdel-Bary
Vol 13, No 2 (2012) Interleukin 6 (IL6) as a predictor outcome in patients with compensated cirrhosis and symptomatic gall stones after cholecystectomy Abstract   PDF
E Ragab, A Hegazy, M Morshed, S El-Awadi, W Khafagi, A Moatamed
Vol 17, No 1 (2016) α-4 subunit of nicotinic acetylcholine receptor polymorphisms exhibit no association with smoking behavior among Malay Males in Kelantan, Malaysia Abstract   PDF
A.B. Ruzilawati, N.I. Abd Rozak, A.B. Norsuhaily, A. Imran
Vol 18, No 1 (2017) Kabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child Abstract   PDF
Rabah M. Shawky, Radwa Gamal, Nayera Mostafa
Vol 14, No 1 (2013) Lack of association between TRAF1/C5 rs10818488 polymorphism and rheumatoid arthritis in Iranian population Abstract   PDF
E Samadian, A Bidmeshkipour, R Gharaei, E Soleymani-Nejadian, A Shirkavand
Vol 15, No 1 (2014) Lack of association of CTLA-4 +49 A/G polymorphism with predisposition to type 1 diabetes in a cohort of Egyptian families Abstract   PDF
AM Kamel, MF Mira, GI Mossallam, GTA Ebid, ER Radwan, NH Aly Eldin, M Mamdouh, M Amin, N Badawy, H Bazaraa, A Ibrahim, N Salah
Vol 14, No 4 (2013) Language impairment in attention deficit hyperactivity disorder in preschool children Abstract   PDF
SR El Sady, AAS Nabeih, EMA Mostafa, AA Sadek
Vol 11, No 1 (2010) L–Carnitine ameliorates the iron mediated DNA degradation in peripheral leukocytes of β-thalassemic children Abstract   PDF
SM Ragab, RG Mahfouz
Vol 19, No 4 (2018) Left ventricle myocardial performance in Down Syndrome children with clinically and anatomically normal hearts: Relationship to oxidative stress Abstract   PDF
Omneya Ibrahim Youssef, Soha Youssef Raouf
Vol 15, No 2 (2014) Leptin, insulin like growth factor-1 and thyroid profile in a studied sample of Egyptian children with Down syndrome Abstract   PDF
HH El Gebali, EA Zaky, SH Agwa, EZ Mohamed
Vol 16, No 2 (2015) Letter to the Editor Abstract   PDF
M Saadat
Vol 16, No 4 (2015) Letter to the Editor Abstract   PDF
Nazurah Alwi, Dzalani Harun, JH Leonard
Vol 19, No 2 (2018) Letter to the Editor: Are we missing fucosidosis? Abstract   PDF
Solaf Elsayed
Vol 14, No 2 (2013) Letter to the editor: Controversial report on sickle cell trait in Manipur, India Abstract   PDF
Maishnam Rustam Singh
Vol 15, No 4 (2014) Letter to the Editor:Hardy–Weinberg equilibrium and association study of insertion/deletion polymorphism of ACE gene and Alzheimer’s disease in Egyptian patients Abstract   PDF
M Saadat
Vol 16, No 4 (2015) Lipoprotein lipase gene variants: Association with acute myocardial infarction and lipid profiles Abstract   PDF
Mahyar Bahrami, Hamzah Barati, Mohammad M Jahani, Ahmad Fatemi, Zohre Sharifi, Akram Eydi, Sadegh Alipoor, Taghi Golmohammadi
Vol 18, No 3 (2017) Long noncoding RNA metastasis-associated lung adenocarcinoma transcript 1 (MALAT1): A molecular predictor of poor survival in glioblastoma multiforme in Egyptian patients Abstract   PDF
Manal S. Fawzy, Eman A. Toraih, Hoda Y. Abdallah
Vol 12, No 2 (2011) Low bone density management via capacitively coupled electrical fields and low intensity pulsed ultrasound in hemiparetic cerebral palsy Abstract   PDF
KA Olama
Vol 9, No 1 (2008) Low Incidence of Androgen Receptor Mutation Among Egyptian Children with Androgen Resistance Abstract   PDF
M Essawi, H Nasr, I Mazen, K Gaafar, K Amr, M Hafez, Y Gad
Vol 16, No 3 (2015) Lower HOMA-β values are detected among individuals with variant of E23K polymorphism of potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11) gene Abstract   PDF
R Sunita, AH Sadewa, A Farmawati
Vol 17, No 1 (2016) Magnesium supplementation in children with attention deficit hyperactivity disorder Abstract   PDF
Farida El Baza, Heba Ahmed AlShahawi, Sally Zahra, Rana Ahmed AbdelHakim
Vol 18, No 2 (2017) Magnesium, zinc and copper estimation in children with attention deficit hyperactivity disorder (ADHD) Abstract   PDF
Farida Elbaz, Sally Zahra, Hussien Hanafy
Vol 14, No 1 (2013) Markers of neural degeneration and regeneration in Down syndrome patients Abstract   PDF
IE Abdel-Meguid, E Abdel-Salam, DMA Latif, S Korraa, A Ismaiel
Vol 15, No 1 (2014) Maternal MTHFR C677T genotype and septal defects in offspring with Down syndrome: A pilot study Abstract   PDF
GM Elsayed, SM Elsayed, SS Ezz-Elarab
Vol 10, No 2 (2009) Maternal risk factors in young Egyptian mothers of Down syndrome Abstract   PDF
RM Shawky, E Elsobky, SM Elsayed, H Kamal, Y Eðin, N Akar
Vol 17, No 4 (2016) Meier–Gorlin syndrome: An additional Egyptian patient with gastroesophageal reflux, hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly Abstract   PDF
Rabah M. Shawky, Radwa Gamal
Vol 16, No 4 (2015) Metabolic abnormalities in young Egyptian women with polycystic ovary syndrome and their relation to ADIPOQ gene variants and body fat phenotype Abstract   PDF
Moushira Zaki, Shams Kholoussi, Somaia Ismail, Haiam Abdel Raouf, Iman Helwa, Naglaa Hassan, Eman Youness, Nadia A Mohamed, Sanaa Kamal, Walaa Yousef, Mohamed Shaker, Wafaa Ezzat, Yasser A Elhosary, Omnia M Saleh, Mona El Gammal, Hala T El-Bassyouni, Samira Ismail, Mamdouh Bibars, Osama Azmy
Vol 18, No 3 (2017) Metabolic derangements in IUGR neonates detected at birth using UPLC-MS Abstract   PDF
M.A. Abd El-Wahed, O.G. El-Farghali, H.S.A. ElAbd, E.D. El-Desouky, S.M. Hassan
Vol 19, No 4 (2018) Metadherin mRNA expression in hepatocellular carcinoma Abstract   PDF
Nevein M. Al-sheikh, Sally M. El-Hefnway, Ahmed M. Abuamer, Ashraf G. Dala
Vol 17, No 2 (2016) Methionine synthase A2756G and reduced folate carrier1 A80G gene polymorphisms as maternal risk factors for Down syndrome in Egypt Abstract   PDF
Maha Moustafa, Elham Gaber, Gamal Abo El Fath
Vol 13, No 2 (2012) Methylenetetrahydrofolate reductase gene polymorphism in type 1 diabetes mellitus: Relationship to microvascular complications Abstract   PDF
MA AboElAsrar, AA Hamed, N Akar, Y Egin, MMM Saied
Vol 13, No 2 (2012) Micro RNA: New aspect in pathobiology of preeclampsia? Abstract   PDF
H Harapan, M Andalas, D Mudhakir, NC Pedroza, SV Laddha, JR Anand
Vol 18, No 4 (2017) Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II Abstract   PDF
Rabah M. Shawky, Radwa Gamal, Shaimaa Abdelsattar Mohammad
Vol 18, No 2 (2017) MicroRNA-146a expression as a potential biomarker for rheumatoid arthritis in Egypt Abstract   PDF
Heba Mohamed Abdelkader Elsayed, Walaa Shawky Khater, Ayman Asaad Ibrahim, Maha Salah El-din Hamdy, Nashwa Aly Morshedy
Vol 11, No 2 (2010) Mitochondrial alterations in children with chronic liver disease Abstract   PDF
RM Shawky, TY Abdel-Gaffar, MA El-Etriby, MS ElMoneiri, NG Elhefnawy, R Elsherif, SM Nour El-Din
Vol 18, No 1 (2017) Mitochondrial control region and GSTP1 polymorphism associated with familial urinary bladder cancer in Karbi-Anglong tribe of Assam, Northeast India Abstract   PDF
Souvik Ghatak, Ravi Prakash Yadav, Hanumath Singh Rathore, Keheibamding Thou, Felix Jakha, K. Toska Sumi, Zothan Sanga, Nachimuthu Senthil Kumar
Vol 13, No 3 (2012) Mitochondrial DNA depletion syndrome presenting with ataxia and external ophthalmoplegia: Case report Abstract   PDF
L Selim, D Mehaney, F Hassan, R Sabry, R Zeyada, S Hassan, IG Eldin, E Bertini
Vol 14, No 3 (2013) Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes in a Japanese child: Clinical, radiological and molecular genetic analysis Abstract   PDF
L Selim, D Mehaney
Vol 12, No 2 (2011) Models to explore the molecular function and regulation of AIRE Abstract   PDF
T Lovewell, R Tazi-Ahnini
Vol 13, No 1 (2012) Modulation of back geometry in children with spastic diplegic cerebral palsy via hippotherapy training Abstract   PDF
GH El-Meniawy, NS Thabet
Vol 13, No 1 (2012) Molecular analysis of MECP2 gene in Egyptian patients with Rett syndrome Abstract   PDF
MS Zaki, WE Sharaf El-Din, GM Hamdy, IH Kamal, AK Abdel Aleem
Vol 17, No 2 (2016) Molecular characterization of X chromosome fragility in idiopathic mental retardation Abstract   PDF
Heba Alla Hosny Omar, Tarek M. Kamal, Heba Salah Abd-Alkhalek, Ghada H. El Nady, MSZ Salem
Vol 12, No 2 (2011) Molecular detection of circulating thyroid specific transcripts (TSHR/Tg-mRNAs) in thyroid cancer patients: Their diagnostic significance Abstract   PDF
SH Teama, SHA Agwa, A Fawzy, MM Sayed, WA Ibrahim, YM Eid
Vol 8, No 2 (2007) Molecular epidemiology of antibiotic-associated diarrhoea due to Clostridium difficile and clostridium perfringens in Ain Shams University Hospitals Abstract   PDF
MA Shaheen, SM Zaki, AA El-Sayed, NM Sayed, AA Abdel Aziz, SA Hamza
Vol 15, No 1 (2014) Molecular fingerprinting of the Egyptian medicinal plant Cocculus pendulus Abstract   PDF
AF Shadia, MES Fareida, AB Sengab, MS Naglaa, AM Osman, SED El-Shaimaa
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ISSN: 1110-8630
AJOL African Journals Online