Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Imen Boudriga"'
Autor:
Ghada Bouguerra, Khaoula Talbi, Nawel Trabelsi, Dorra Chaouachi, Imen Boudriga, Salem Abbès, Samia Menif
Publikováno v:
Cellular Physiology and Biochemistry, Vol 55, Iss 6, Pp 761-772 (2021)
Externí odkaz:
https://doaj.org/article/4d4de2fd699147ba90815c868eb7ed21
Autor:
Miniar Kalai, Imen Moumni, Houyem Ouragini, Ilhem Ben Fraj, Fethi Mellouli, Monia Ouederni, Dorra Chaouachi, Imen Boudriga, Samia Menif
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 60:81-85
Background Deletions in the β-globin cluster are uncommon and cause thalassemia (thal) with hereditary persistence of fetal hemoglobin. They constitute a heterogenous group of disorders characterized by absent or reduced synthesis of adult hemoglobi
Autor:
Mouna, Jaouani, Nadia, Hamdi, Leila, Chaouch, Miniar, Kalai, Fethi, Mellouli, Imen, Darragi, Imen, Boudriga, Dorra, Chaouachi, Mohamed, Bejaoui, Salem, Abbes
Publikováno v:
In Egyptian Journal of Medical Human Genetics July 2016 17(3):265-270
Publikováno v:
American journal of perinatology.
Objective In this study, we report a Tunisian newborn boy referred for neonatal hemolytic anemia with yellowish skin and enlarged spleen due to coinheritance of hemoglobin O (HbO) Arab and β-thalassemia. Study Design Hematological parameters were co
Autor:
Raouf Hafsia, Meriem Oueslati, Salem Abbes, Nawel Trabelsi, Wijdene Elborgi, Dorra Chaouachi, Imen Boudriga, Faten Haddad, Imen Darragi, Leila Chaouch, Houyem Ouragini
Publikováno v:
Hemoglobin. 41(2)
We report here the clinical, hematological and molecular data in a 50-year-old patient with β-thalassemia intermedia (β-TI) caused by a homozygous β+ mutation on the β-globin gene polyadenylation (polyA) signal (AATAAA>AAAAAA). β Haplotype analy