Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hadef Skouri"'
Autor:
Houda Ajmi, Sameh Mabrouk, Saida Hassayoun, Haifa Regaieg, Minyar Tfifha, Chemli Jalel, Hadef Skouri, Noura Zouari, Saoussan Abroug
Publikováno v:
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-4 (2017)
Abstract Background Autoimmune hemolytic anemia is rare in children. First-line therapies for this disease consist of corticosteroids and intravenously administered immunoglobulin that are effective in most patients. However, a small proportion of ca
Externí odkaz:
https://doaj.org/article/ec4692080df84e71b63b6c68d36b3391
Autor:
Minyar Tfifha, S. Hassayoun, H. Ajmi, Hadef Skouri, N. Zouari, Chemli Jalel, Sameh Mabrouk, Haifa Regaieg, S. Abroug
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-4 (2017)
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-4 (2017)
Background Autoimmune hemolytic anemia is rare in children. First-line therapies for this disease consist of corticosteroids and intravenously administered immunoglobulin that are effective in most patients. However, a small proportion of cases (5 to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af83538ca7ffd0110fdc0dd66870174d
https://pubmed.ncbi.nlm.nih.gov/29132419
https://pubmed.ncbi.nlm.nih.gov/29132419
Publikováno v:
Journal of Clinical Laboratory Analysis. 26:167-173
Specific genetic conditions are known to be associated with high risk of venous thromboembolism. This genetic basis varies widely between ethnic groups. We investigated the distribution of four inherited polymorphisms in 113 unselected Tunisian blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd61574a31c20eac4369f28134e452d7
https://doi.org/10.1002/jcla.21506
https://doi.org/10.1002/jcla.21506
Autor:
Samira, Hadhri, Mohamed Ben, Rejab, Hajer, Guedria, Lamia, Ifa, Noureddine, Chatti, Hadef, Skouri
Publikováno v:
Journal of clinical laboratory analysis. 26(3)
Specific genetic conditions are known to be associated with high risk of venous thromboembolism. This genetic basis varies widely between ethnic groups. We investigated the distribution of four inherited polymorphisms in 113 unselected Tunisian blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b45ee6892b97f9b949f02483ec85431e
https://pubmed.ncbi.nlm.nih.gov/22628232
https://pubmed.ncbi.nlm.nih.gov/22628232
Autor:
Imen Kraiem, Henda El Euch, Saoussen Abroug, Abdelaziz Harbi, Hadef Skouri, Jalel Gargouri, Raoudha Gandouz
Publikováno v:
American journal of hematology. 81(5)
Heparin, which is used at high doses in hemodialysis patients, may induce antibodies favoring thromboembolic complications. We prospectively investigated the prevalence of heparin-induced platelet-reactive antibodies in a cohort of 38 pediatric hemod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edd493415f6be82a6aae563da98bc71a
https://pubmed.ncbi.nlm.nih.gov/16628723
https://pubmed.ncbi.nlm.nih.gov/16628723
Autor:
Halima, el Omri, Imen, Kraiem, Habib, Amara, Yosra, Ben Youssef, Hadef, Skouri, Souad, Ennabli
Publikováno v:
La Tunisie medicale. 80(5)
Primary renal non Hodgkin lymphoma is rare and unusual because the renal parenchyma does not have lymphatics. We report a case of bilateral primary lymphoblastic T lymphoma presenting with renal insufficiency in a 14 year old girl. We discuss clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4773c59f64fd993818e6c530477392db
https://pubmed.ncbi.nlm.nih.gov/12534038
https://pubmed.ncbi.nlm.nih.gov/12534038
Autor:
Hadef Skouri, Raoudha Gandouz, Saoussen Abroug, Imen Kraiem, Henda Euch, Jalel Gargouri, Abdelaziz Harbi
Publikováno v:
American Journal of Hematology; May2006, Vol. 81 Issue 5, p328-334, 7p