Published: 2019-01-14




Helicobacter pylori Western cagA genotype in Egyptian patients with upper gastrointestinal disease

Manal Diab, Mohamed Shemis, Doaa Gamal, Ahmed El-Shenawy, Maged El-Ghannam, Effat El-Sherbini, Mohamed Saber

297-300



Angiotensin-converting enzyme (ACE) I/D and bradykinin B2 receptor T/C genes polymorphism in patients with ACE inhibitors-related cough

Mohammad Saifur Rohman, Jonny Karunia Fajar, Bagus Hery Kuncahyo, Lowry Yunita, Erdo Puncak Sidarta, Putu Nina Belinda Saka, Teuku Heriansyah, Nashi Widodo

307-313


Study of DNA methyl transferase 3A mutation in acute myeloid leukemic patients

Ghada M. Elsayed, Abd Elgawad A. Fahmi, Nevine F. Shafik, Reham A.A. Elshimy, Heba K. Abd Elhakeem, Sara A. Attea

315-319





FLT3 receptor/CD135 expression by flow cytometry in acute myeloid leukemia: Relation to FLT3 gene mutations and mRNA transcripts

Mohamed Amin Mekawy, Deena Samir Eissa, Mohamed Tarif Hamza, Gehan Mostafa Hamed, Mariam Karam Youssef

345-351


Evaluation of health-related quality of life and muscular strength in children with beta thalassemia major

Dina K. Ismail, Mona H. El-Tagui, Zeinab A. Hussein, Mohamed A. Eid, Sobhy M. Aly

353-357


Study of congenital malformations in infants and children in Menoufia governorate, Egypt

Soheir S. AbouEl-Ella, Maha A. Tawfik, Wafaa Moustafa M. Abo El-Fotoh, Mai A. Elbadawi

359-365



Renalase gene polymorphisms (rs2576178 and rs10887800) in Egyptian hypertensive end stage renal disease patients

Noha S. Kandil, Rania Mohamed El Sharkawy, Lubna Mohamed Ibrahim Desouky, Lamia Said Kandil, I.M. Masoud, Noha Gaber Amin

379-383



Metadherin mRNA expression in hepatocellular carcinoma

Nevein M. Al-sheikh, Sally M. El-Hefnway, Ahmed M. Abuamer, Ashraf G. Dala

391-397





Detection of antimicrobial resistance genes of Helicobacter pylori strains to clarithromycin, metronidazole, amoxicillin and tetracycline among Egyptian patients

Manal Diab, Ahmed El-Shenawy, Maged El-Ghannam, Dalia Salem, Moustafa Abdelnasser, Mohamed Shaheen, Mahmoud Abdel-Hady, Effat El-Sherbini, Mohamed Saber

417-423


Genetic study of the NOTCH3 gene in CADASIL patients

Seyedeh Parisa Chavoshi Tarzjani, Seyed Abolhassan Shahzadeh Fazeli, Mohammad Hossein Sanati, Zahra Mirzayee

425-427


Cantu syndrome in an Egyptian child

Rabah M. Shawky, Radwa Gamal

429-432


Asymptomatic hemochromatosis case with HFE c.1007-47G>A, c.340+4T>C heterozygous mutations and alpha globin -3.7 kb deletion

Vesile Deniz Çelik, Betul Orhan Kiliç, Yasemin Ardıçoğlu Akışin, Fatma Ajlan Tükün, Nejat Akar

433-435



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eISSN: 1110-8630