Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nawel Trabelsi"'
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:
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
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:
Nawel Trabelsi
Hereditary spherocytosis (HS) is an inherited disorder characterized by intrinsic defects in the red cell membrane proteins. The molecular abnormality is heterogeneous and may affect several membrane proteins including spectrin, ankyrin, band 3 and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9d1891b6d6d1e54cff77b8df768c012
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