Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Houyem, Ouragini"'
Publikováno v:
HemaSphere, Vol 7, p e140481b (2023)
Externí odkaz:
https://doaj.org/article/48e977a306de442cbc8246c5ead1b7f2
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:
Houyem Ouragini, Sonia Nouira, Emna Bouatrous, Monia Ouederni, Salem Abbes, Samia Menif, Monia Ben Khaled
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:e1055-e1058
Several causes are known to be at the origin of neonatal cyanosis among them methemoglobinemia is by inheritance of an hemoglobin (Hb) M variant. This is a rare condition never been reported in Tunisia so far. Here, we report a Tunisian newborn with
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:
Naima Saidani, Emna Bouatrous, Houyem Ouragini, Amira Ayachi, Imen Kraiem, Imen Boudrigua, Ons Laabidi, Samia Menif, Dorra Chaouachi, Sana Zitouni, Salem Abbes, Mechaal Mourali
Publikováno v:
American journal of perinatology. 39(11)
This study was aimed to establish local reference values for hematological indices and hemoglobin (Hb) fractions in umbilical cord blood (UCB) for the northern population of Tunisia.Our study included full-term newborns by vaginal deliveries. Hematol
Publikováno v:
Acta cardiologica. 75(7)
Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare disease presenting with syncopal events and sudden cardiac death at a young age in the absence of structural heart disease. Two major genes have been shown to be respo
Autor:
Imen Darragi, Salem Abbes, Imen Boudrigua, Miniar Kalai, Houyem Ouragini, Mouna Ben Sassi, Raouf Hafsia, Leila Chaouch, Imen Moumni, Dorra Chaouachi
Publikováno v:
Acta Haematologica Polonica. 47:242-247
Background and aim Sickle cell anemia (SCA) is characterized by variable patterns of clinical expression. Polymorphisms linked to different genes have been associated with specific complications of the disease. Herein, we focused on the study of the
Autor:
Slim Ben Ammar, Neji Tebib, Farah Ouechtati, Khaled Lasram, Marie Françoise Ben Dridi, Faten Talmoudi, Rym Kefi, Houyem Ouragini, Nizar Ben Halim, Insaf Rejeb, Olfa Messaoud, Asma Walha, Yosra Bouyacoub, Sonia Abdelhak, Mourad Mokni, Ahlem Amouri, Habib Messai, Sana Hsouna, Majdi Nagara, Ahlem Sabrine Ben Brick, Wafa Cherif, Leila El Matri, Faten Ben Rhouma, I. Chouchene, Mariem Ben Rekaya
Publikováno v:
American Journal of Human Biology. 28:171-180
Objectives Consanguinity is common in Tunisia. However, little information exists on its impact on recessive disorders. In this study, we evaluate the impact of consanguineous marriages on the occurrence of some specific autosomal recessive disorders
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
Autor:
Imen Moumni, Dorra Chaouachi, Imen Darragi, Marwa Dridi, Fethi Mellouli, Miniar Kalai, Salem Abbes, Mohamed Bejaoui, Leila Chaouch, Imen Boudrigua, Houyem Ouragini
Publikováno v:
Hematology (Amsterdam, Netherlands). 22(3)
Mediators of adhesion become a potential new target for pharmacological therapy to struggle the complications of sickle cell disease (SCD). Several mechanisms for increased adherence have been postulated and the well-studied are CD36 and VLA4 which e