Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sabrine Haloui"'
Autor:
Latifa Jouini, Sabrine Haloui, Amina Bibi, Chaima Abdelhafidh Sahli, Rym Daboubi, Nourelhouda Toumi, Taieb Messsaoud, Naouel Laouini, Hajer Siala, Faida Ouali, Sondes Hadj Fredj, Meriam Becher
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 55:1193-1201
Background:Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the commonest enzymopathy worldwide. The incidence depends essentially on the methods used for the assessment. In this respect, we attempted in this study to set cut-off values of G6PD
Autor:
Sihem Barsaoui, Nour El Houda Toumi, Semia Cherif, Rim Othmani, Rim Daboubi, Faida Ouali, Monia Khemiri, Sondess Hadj Fredj, Sabrine Haloui, Taieb Messaoud, Naouel Laouini, Latifa Jouini, K. Kazdaghli, Chaima Abdelhafidh Sahli, Mariem Becher, Hajer Siala, Faten Tinsa, Amina Bibi
Publikováno v:
Annales de biologie clinique. 74(2)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymopathy. More than 200 mutations in the G6PD gene have been described. In Tunisia, the A-African and the B-Mediterranean mutations predominate the mutational spectrum. The pur
Autor:
Faida Ouali, Hajer Siala, S. Hadj Fredj, S. Amdouni, N. Ben Romdhane, T. Messsaoud, Fattoum S, R. Othmani, Sabrine Haloui, Nour El Houda Toumi, Naouel Laouini, Amina Bibi, Chaima Abdelhafidh Sahli, K. Kazdaghli, H. Ammar, Latifa Jouini
Publikováno v:
Molecular Biology Reports. 40:851-856
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect. In this study, we aimed to perform a molecular investigation of G6PD deficiency in Tunisia and to associate clinical manifestations and the degree of deficien