PROMOTING ACCESS TO AFRICAN RESEARCH

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Issue Title
 
Vol 13, No 2 (2012) Case Report - Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome Abstract   PDF
RM Shawky, NS Elsayed, NS Seifeldin
 
Vol 13, No 3 (2012) Case Report - Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with lissencephaly and brain cyst Abstract   PDF
RA Abolila, RM Alsawan, MT Alrefaie
 
Vol 13, No 2 (2012) Case Report - Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome) in an Egyptian child with premature loss of teeth, and café au lait skin patches Abstract   PDF
RM Shawky, HS Abd-Elkhalek, S Gad, NS Seifeldin
 
Vol 13, No 3 (2012) Case Report - Serious life threatening upper airway obstruction in congenital generalized myofibromatosis Abstract   PDF
RA Abolila, RM Alsawan, HA Masud
 
Vol 16, No 3 (2015) CASE REPORT Moebius syndrome with macular hyperpigmentation, skeletal anomalies, and hypoplasia of pectoralis major muscle in an Egyptian child Abstract   PDF
RM Shawky, R Gamal, SA Mohammad
 
Vol 19, No 3 (2018) Case Report: A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia Abstract   PDF
Didem Torun Özkan, Nejat Akar
 
Vol 15, No 1 (2014) Case Report: Allgrove syndrome: an Egyptian family with two affected siblings Abstract   PDF
OH Gebril
 
Vol 15, No 2 (2014) Case Report: Bilateral absence of fifth ray in feet, cleft palate, malformed ears, and corneal opacity in a patient with Miller syndrome Abstract   PDF
RM Shawky, N Amr, H Salah, S Gad
 
Vol 15, No 1 (2014) Case Report: Bilateral iris, choroid, optic nerve colobomas and retinal detachment in an Egyptian patient with mild Baraitser–Winter syndrome Abstract   PDF
RM Shawky, HSAE Elabd, R Gamal
 
Vol 15, No 1 (2014) Case Report: Intrafamilial variability in Simpson–Golabi–Behmel syndrome with bilateral posterior ear lobule creases Abstract   PDF
RM Shawky, HS Abd-Elkhalek, S Gad
 
Vol 15, No 4 (2014) Case Report: Meier-Gorlin syndrome: Report of an additional patient with congenital heart disease Abstract   PDF
R M Shawky, H S Abd-Elkhalek Elabd, R Gamal, S A Mohammad, S Gad
 
Vol 13, No 1 (2012) Case Report: Multiple pterygium syndrome with marked pterygia of the fingers and MRI changes in the spine Abstract   PDF
RM Shawky, S Elsayed, N Gaboon
 
Vol 15, No 4 (2014) Case Report: Oral–Facial–Digital Syndrome type VI with self mutilations Abstract   PDF
R M Shawky, H S Abd-Elkhalek Elabd, S Gad, R Gamal, S A Mohammad
 
Vol 16, No 1 (2015) Case Report: Primary ciliary dyskinesia: Kartagener syndrome in a family with a novel DNAH5 gene mutation and variable phenotypes Abstract   PDF
MJ Marafie, IS Al Suliman, AM Redha, AM Alshati
 
Vol 15, No 2 (2014) Case Report: Senior-Loken syndrome: A novel NPHP5 gene mutation in a family from Kuwait Abstract   PDF
MJ Marafie, F Al-Mulla
 
Vol 16, No 1 (2015) Case Report: Trichorhinophalangeal syndrome II, expanding the clinical spectrum Abstract   PDF
RM Shawky, HSA Elkhalek, AES Elghawaby, SA Mohammad, NS Seifeldin
 
Vol 13, No 1 (2012) Case Report: Trigonocephaly and Dandy walker variant in an Egyptian child – Probable mild Opitz trigonocephaly C syndrome Abstract   PDF
RM Shawky, HS Abd-Elkhalek
 
Vol 14, No 2 (2013) Case Report

Hypothyroidism could be the only manifestation of mitochondrial T8993C mutation in Leigh syndrome
Abstract   PDF
Hoda Tomoum, Solaf M Elsayed, Elizabeth Berry-Kravis
 
Vol 10, No 2 (2009) Caveolin 3 gene and mitochondrial tRNA methionin gene in Duchenne muscular dystrophy Abstract   PDF
IE Abdel-Meguid, SS Korraa, E Abdel-Salam
 
Vol 17, No 3 (2016) Challenges identified in the management of patients with inherited metabolic disorders – A five year experience from Pakistan Abstract   PDF
Bushra Afroze, Laila Lakhani, Farah Naz, Sana Somani, Zabedah Md. Yunus, Nick Brown
 
Vol 17, No 3 (2016) Challenges in diagnosis and counseling of a family with two recessive neurometabolic disorders Abstract   PDF
Heba S Abd-Elkhalek, Radwa Gamal, Osama K Zaki, Solaf M Elsayed
 
Vol 15, No 4 (2014) Chemopreventive effect of Annona muricata on DMBA-induced cell proliferation in the breast tissues of female albino mice Abstract   PDF
J B Minari
 
Vol 9, No 2 (2008) Cholestasis in neonates and infants Abstract   PDF
A Elfaramawy
 
Vol 17, No 4 (2016) Christ-Siemens-Touraine syndrome with cleft palate, absent nipples, gallstones and mild mental retardation in an Egyptian child Abstract   PDF
Rabah M. Shawky, Radwa Gamal
 
Vol 17, No 1 (2016) Chromosomal abnormalities and autism Abstract   PDF
Farida El-Baz, Mohamed Saad Zaghloul, Ezzat El Sobky, Reham M Elhossiny, Heba Salah, Neveen Ezy Abdelaziz
 
Vol 12, No 1 (2011) Chromosomal study in newborn infants with congenital anomalies in Assiut University hospital: Cross-sectional study Abstract   PDF
YA Mohammed, RM Shawky, AS Soliman, MM Ahmed
 
Vol 13, No 3 (2012) Chromosome 22 microdeletion in children with syndromic congenital heart disease by fluorescent in situ hybridization (FISH) Abstract   PDF
SSA El-Ella, F El Gendy, MAM Tawfik, E El Sobky, A Khattab, M El-mekkawy
 
Vol 17, No 1 (2016) Circulating cell free DNA as a predictor of systemic lupus erythematosus severity and monitoring of therapy Abstract   PDF
Olfat M. Hendy, Tawfik Abdel Motalib, Mona A. El Shafie, Fatma A. Khalaf, Sobhy E. Kotb, Aziza Khalil, Salwa R. Ali
 
Vol 11, No 2 (2010) Circulating MCP-1 level and 2518 gene polymorphism as a marker of nephropathy development in Egyptian patients Abstract   PDF
AM Hassan, H Nagy, WS Mohamed
 
Vol 18, No 2 (2017) Circulating MiRNA-21 and programed cell death (PDCD) 4 gene expression in hepatocellular carcinoma (HCC) in Egyptian patients Abstract   PDF
Gamalat El Gedawy, Manar Obada, Ayman Kelani, Hala El-Said, Naglaa M. Ghanayem
 
Vol 18, No 3 (2017) Clinical and genetic assessment of pediatric patients with Gaucher’s disease in Upper Egypt Abstract   PDF
Tahia H. Saleem, Mohammed H. Hassan, Ahmed El-Abd Ahmed, Ayat A. Sayed, Nahed A. Mohamed, Khalid I. Elsayh, Abdallah M.A.A. El-Ebidi, Norhan B.B. Mohammed
 
Vol 14, No 1 (2013) Clinical and molecular findings in eight Egyptian patients with suspected mitochondrial disorders and optic atrophy Abstract   PDF
GMM Al-Ettribi, LK Effat, HT El-Bassyouni, MS Zaki, G Shanab, AM Karim
 
Vol 14, No 1 (2013) Clinical and molecular findings in eight Egyptian patients with suspected mitochondrial disorders and optic atrophy Abstract   PDF
GMM Al-Ettribi, LK Effat, HT El-Bassyouni, MS Zaki, G Shanab, AM Karim
 
Vol 10, No 1 (2009) Clinical, anthropometric, radiological and molecular characteristics of Egyptian achondroplasia patients Abstract   PDF
MS Aglan, AK Abdel-Aleem, A IS EL-Katoury, MH Hafez, SN Saleem, GA Otaify, SA Temtamy
 
Vol 14, No 2 (2013) Clinical characteristics and analysis of HFE gene variants (C282Y and H63D) in Jordanian Arab patients with age-related macular degeneration Abstract   PDF
Asem Alkhateeb, Shadi Al-khatib, Ahmed Elbetieha, Tasnim Al-Rashaideh
 
Vol 18, No 1 (2017) Clinical profile of cyanotic congenital heart disease in neonatal intensive care unit at Sohag University Hospital, Upper Egypt Abstract   PDF
Ashraf Abou-Taleb, Marwa A. Abdelhamid, Mohamed A.M. Bahkeet
 
Vol 19, No 2 (2018) Clinical Utility of promoter methylation of the tumor suppressor genes DKK3, and RASSF1A in breast cancer patients Abstract   PDF
Marwa H. Saied, Aya Samy Rady, Galal Mustafa Abo El Naga, Ola A. Sharaki
 
Vol 12, No 1 (2011) Clinico-epidemiologic characteristics of spinal muscular atrophy among Egyptians Abstract   PDF
RM Shawky, NS El-Sayed
 
Vol 11, No 2 (2010) Clinico-epidemiologic features of oculocutaneous albinism in northeast section of Cairo – Egypt Abstract   PDF
AF Mohamed, NS El-Sayed, NS Seifeldin
 
Vol 14, No 3 (2013) Clinicolaboratory profile of phenylketonuria (PKU) in Sohag University Hospital-Upper Egypt Abstract   PDF
AA Sadek, AM Emam, MY Alhaggagy
 
Vol 12, No 1 (2011) Colchicine resistant FMF is not always true resistance Abstract   PDF
TYA Ghaffar, SM Elsayed
 
Vol 12, No 1 (2011) Colchicine resistant FMF is not always true resistance Abstract   PDF
TYA Ghaffar, SM Elsayed
 
Vol 13, No 2 (2012) Combined effects of myofeedback and isokinetic training on hand function in spastic hemiplegic children Abstract   PDF
KA Olama, FA Hegazy, NS Thabt
 
Vol 11, No 1 (2010) Common MEFV mutations in Egyptian patients with familial Mediterranean fever Abstract   PDF
M El Sayed, N Elazizi, AM Ibrahim, T Zaher, M Hashem
 
Vol 19, No 1 (2018) Common variant of 5,10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian population Abstract   PDF
Marzieh Attar, Seyedpayam Shirangi, Farnoosh Shateri, Majid Shahbazi
 
Vol 16, No 2 (2015) Comparative frequency and allelic distribution of ABO and Rh (D) blood groups of major tribal communities of southern Bangladesh with general population and their determinants Abstract   PDF
G Dewan
 
Vol 14, No 3 (2013) Comparative study: Parameters of gait in Down syndrome versus matched obese and healthy children Abstract   PDF
SA Elshemy
 
Vol 11, No 2 (2010) Comparing effects of interleukin-2 and interleukin-4 on the expression of MHC class II, CD80 and CD86 on polymorphonuclear neutrophils Abstract   PDF
BKA-H Abdel-Salam
 
Vol 14, No 4 (2013) Comparison of broad range 16S rDNA PCR to conventional blood culture for diagnosis of sepsis in the newborn Abstract   PDF
NI Draz, SE Taha, NM Abou Shady, YS Abdel Ghany
 
Vol 18, No 4 (2017) Comparison of multiplex reverse transcription-PCR-enzyme hybridization assay with immunofluorescence techniques for the detection of four viral respiratory pathogens in pediatric community acquired pneumonia Abstract   PDF
Mervat Gamal Eldin Mansour, Sherin Albendary
 
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ISSN: 1110-8630
AJOL African Journals Online