Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Faten Haddad"'
Autor:
Nawel Trabelsi, Ghada Bouguerra, Faten Haddad, Monia Ouederni, Imen Darragi, Imen Boudrigua, Dorra Chaouachi, Mbarka Barmat, Chaker Fouzai, Mohamed Bejaoui, Samia Menif, Imen Kraiem, Salem Abbes
Publikováno v:
Cellular Physiology and Biochemistry, Vol 55, Iss 1, Pp 117-129 (2021)
Externí odkaz:
https://doaj.org/article/dfaaabcdd6f94502879de79c424c2da2
Autor:
Mohamed Bejaoui, Samia Menif, Mbarka Barmat, Salem Abbes, Imen Boudrigua, Imen Darragi, Imen Kraiem, Nawel Trabelsi, Dorra Chaouachi, Monia Ouederni, Faten Haddad, Ghada Bouguerra, Chaker Fouzai
Publikováno v:
Cellular Physiology and Biochemistry, Vol 55, Iss 1, Pp 117-129 (2021)
Background/Aims: Hereditary Spherocytosis (HS) is the most common erythrocyte membrane disorder causing hemolytic anemia. The wide heterogeneity of both clinical and laboratory manifestations of HS contributes to difficulties associated with the diag
Publikováno v:
La Tunisie medicale. 97(12)
To evaluate the contribution of parecoxib to the protocol of multimodal analgesia for simple vesicular lithiasis by laparoscopy.A prospective, randomized, double-blind study was carried out at Habib Thameur Hospital (Tunis). We included 60 patients,
Publikováno v:
La Tunisie medicale. 97(11)
Health care-associated infections are a real public health problem. Contaminated medical equipments such as stethoscopes are often an overlooked vector. In our study, we were interested in proving our doctors stethoscopes contamination and in studyin
Autor:
Nawel Trabelsi, Aminetou Abba, Mohamed Lemine Ould Salem, Sidi M. Ghaber, Faten Haddad, Salem Abbes, Imen Darragi
Publikováno v:
Hemoglobin. 42:7-10
Unstable hemoglobins (Hbs) are a group of Hb disorders that could be the origin of chronic hemolytic anemia. Most of these disorders are caused by point mutations taking place in the globin genes and affecting the stability of the Hb molecule. They a
Autor:
Emna Barkaoui, Imen Boudrigua, Faten Haddad, Nawel Trabelsi, Samia Menif, Salem Abbes, Dorra Chaouachi, Imen Darragi, Leila Chaouch, Mouna Jaouani
Publikováno v:
European Journal of Medical Genetics. 64:104139
Introduction Unconjugated hyperbilirubinemia (UCB) is a feature of Gilbert's syndrome (GS) and Crigler-Najjar's syndrome (CNS), which are two hereditary defects in bilirubin metabolism. Both syndromes are linked to mutations in the UGT1A1 gene, which
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
Publikováno v:
Intensive Care Medicine Experimental
Autor:
Mariem Ben Romdhane, Asma Ben Souissi, Abir Riahi, Faten Haddad, Mhamed S. Mebazaa, S. Kamoun, Maroua Sboui
Publikováno v:
Anesthésie & Réanimation. 1:A232-A233
Introduction L’hypovolemie est frequente en perioperatoire, notamment en urgence, et passe souvent inapercue. Un monitorage peroperatoire de la volemie peut etre utile afin d’optimiser le remplissage et le debit cardiaque. Le doppler œsophagien