Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Dorra Chaouachi"'
Publikováno v:
HemaSphere, Vol 7, p e140481b (2023)
Externí odkaz:
https://doaj.org/article/48e977a306de442cbc8246c5ead1b7f2
Publikováno v:
HemaSphere, Vol 7, p e92036d6 (2023)
Externí odkaz:
https://doaj.org/article/6f74de287ae24274a9291267a533a4ad
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:
Leila Chaouch, Miniar Kalai, Manel Ben Jbara, Arij Ben Chaabene, Imen Darragi, Dorra Chaouachi, Fethi Mallouli, Raouf Hafsia, Abderraouf Ghanem, Salem Abbes
Publikováno v:
Biomedical Papers, Vol 159, Iss 1, Pp 145-149 (2015)
Aims: The skeletal manifestations of sickle cell disease are the result of changes in bone and bone marrow caused by chronic tissue hypoxia that is exacerbated by episodic occlusion of the microcirculation by the abnormal sickle cells. Furthermore, t
Externí odkaz:
https://doaj.org/article/ff6c76f4151f4f91bc425bf5c7cf1453
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bd428a9142785beb5e665e2ea4d0f34
https://doi.org/10.1177/00045632221134688
https://doi.org/10.1177/00045632221134688
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
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30b3c518fb926b1127e15a7e77018cf9
https://pubmed.ncbi.nlm.nih.gov/33667330
https://pubmed.ncbi.nlm.nih.gov/33667330
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::769c10554cefba4125ce987f0db23a5b
https://pubmed.ncbi.nlm.nih.gov/33374024
https://pubmed.ncbi.nlm.nih.gov/33374024