Zobrazeno 1 - 10 of 117 pro vyhledávání: '"Emna GOUIDER"'
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Akademický článek
Von Willebrand Disease laboratory diagnosis in a low middle income country
Autor: O.N.S. GHALI, Hajer Mahmoudi, Fatma Ben Lakhal, Sarra Fekih Salem, Anis Fadhlaoui, Emna Gouider, Wijdene Elborgi
Publikováno v: Journal of Taibah University Medical Sciences, Vol 18, Iss 6, Pp S5- (2023)
Externí odkaz: https://doaj.org/article/2dae993095854f7e92c7edaf2ca46968
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4
Akademický článek
Activated Partial Thromboplastin Time Clot Waveform Analysis In Hemophilia A
Autor: Maha Said, Amani Jabri, Ons Ghali, Fatma Ben Lakhal, Sarra Fekih Salem, Emna Gouider, Wijdene El Borgi
Publikováno v: Journal of Taibah University Medical Sciences, Vol 18, Iss 6, Pp S14- (2023)
Externí odkaz: https://doaj.org/article/5bb3fcff1b4946d6af02cf53f82e9eb4
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Molecular heterogeneity of factor XI deficiency in Tunisia
Autor: Maroua, Gharbi, Hejer, Elmahmoudi, Wejden, ElBorgi, Cherifa, Ouardani, Meriem, Achour, Emna, Gouider
Publikováno v: Blood Coagulation & Fibrinolysis. 33:310-314
Factor XI (FXI) deficiency is a rare inherited bleeding disorder that is highly prevalent in Ashkenazi Jewish ancestry but sporadically observed in most ethnic groups. It is heterogeneous both in clinical presentation and in genetic causality. Althou
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3275574aee50f67ce55280a72050d0b
https://doi.org/10.1097/mbc.0000000000001142
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6
Clinical phenotype and F7 gene genotype in 40 Tunisian patients with congenital factor VII deficiency
Autor: Cherifa, Ouardani, Hejer, Elmahmoudi, Wejden, ELborgi, Maroua, Gharbi, Achour, Meriem, Emna, Gouider
Publikováno v: Blood Coagulation & Fibrinolysis. 33:280-284
Congenital factor VII (FVII) deficiency is an autosomal recessive bleeding disorder characterized by a weak phenotypic and genotypic correlation. This study aimed to determine the genetic alterations of 40 Tunisian patients and to evaluate their rela
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae6d6e9dc5d9ba117eb0febab416d539
https://doi.org/10.1097/mbc.0000000000001139
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7
Low dose prophylaxis and antifibrinolytics: Options to consider with proven benefits for persons with haemophilia
Autor: Manuel Carcao, Emna Gouider, Runhui Wu
Publikováno v: Haemophilia. 28:26-34
Prophylaxis has become standard of care for persons with severe phenotype haemophilia (PWsH). However, 'standard prophylaxis' with either factor or non-factor therapies (emicizumab) is prohibitively expensive for much of the world. We sought to evalu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ae9f21ed15fdcfb2f3cfc80d2146634
https://doi.org/10.1111/hae.14552
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9
Factor XI deficiency: About 20 cases and literature review
Autor: Yosra, Dhaha, Wijdène, El Borgi, Hajer, Elmahmoudi, Mariem, Achour, Sarra, Fekih Salem, Fatma, Ben Lakhal, Balkis, Meddeb, Emna, Gouider
Publikováno v: La Tunisie medicale. 100(1)
Factor XI deficiency is a rare coagulation disorder with variable bleeding manifestations.To evaluate the correlation between the degree of factorXI deficiency and the clinical expression of the disease.Retrospective study, spanning 10 years from Jan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9b3ded08d57d4a706e7126f94dc352d8
https://pubmed.ncbi.nlm.nih.gov/35822334
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