Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Hejer Elmahmoudi"'
Autor:
Hejer Elmahmoudi, Chourouk JBALI, Sawsen BESBES, Rabeb BARRED, Rayhane BELAKHAL, Emna GOUIDER, Hajer ELMAHMOUDI
Publikováno v:
Journal of Taibah University Medical Sciences, Vol 18, Iss 6, Pp S4- (2023)
Externí odkaz:
https://doaj.org/article/49db487e00a944f8b546c7d1003d6d66
Publikováno v:
Journal of Taibah University Medical Sciences, Vol 18, Iss 6, Pp S9- (2023)
Externí odkaz:
https://doaj.org/article/60f63d371a2a470e9543281806605c17
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
https://doi.org/10.1097/mbc.0000000000001142
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
https://doi.org/10.1097/mbc.0000000000001139
Autor:
Kaouther Zahra, Emna Gouider, Meriem Achour, Balkis Meddeb, Hend Ben Neji, Nejla Belhedi, Hejer Elmahmoudi
Publikováno v:
Journal of Hematology
Background: The Glanzmann’s thrombasthenia (GT) is a rare autosomal-recessive bleeding disorder with uncommon neonatal revelation. It is due to abnormalities of quantitative and/or qualitative α IIb β 3 integrin. This cell adhesion receptor is es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4ceb8e69290b058bcd92732f11b57f6
http://europepmc.org/articles/PMC7155826
http://europepmc.org/articles/PMC7155826
Autor:
Meriem Achour, Kaouther Zahra, W. Saied, L. Jouini, Hejer Elmahmoudi, B. Meddeb, Emna Gouider
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 23(1)
Introduction Low dose prophylaxis could be recommended in countries with limited resources. Aim We report our single centre experience in children with haemophilia. Patients Fifty-five children were included in our study with a weekly median dose of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d8fbf7653e355ae3ca5a9f9542c8dbc
https://pubmed.ncbi.nlm.nih.gov/27943510
https://pubmed.ncbi.nlm.nih.gov/27943510
Autor:
M. Zorgan, Kaouther Zahra, Balkis Meddeb, Fatma Ben-lakhal, A. Chalbi, W. Borji, Emna Gouider, Hejer Elmahmoudi
Publikováno v:
Haemophilia. 18:e400-e403
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9101df6f6b8a46c3a6214d4ab6a4123f
https://doi.org/10.1111/j.1365-2516.2012.02930.x
https://doi.org/10.1111/j.1365-2516.2012.02930.x
Autor:
Rim Sassi, Emna Gouider, Hejer Elmahmoudi Abdallah, Houssein Khodjet-El-Khil, Balkis Meddeb, Adel Hamza, Raouf Hafsia, Nejla Stambouli, Asma Jlizi, Amel Benammar Elgaaied, Nejla Belhedi, Mohamed Ben Amor
Publikováno v:
Blood Cells, Molecules, and Diseases. 44:120-123
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::200664fb621515a45eeccbd37921bdcb
https://doi.org/10.1016/j.bcmd.2009.11.004
https://doi.org/10.1016/j.bcmd.2009.11.004
Autor:
Kaouther Zahra, Amel Ben Ammar Elggaaied, Balkis Meddeb, Hejer Elmahmoudi, Christine Vinciguerra, Emna Gouider, Asma Jlizi, Houssein Khodjet-El-Khil, Edvard Wigren, Dorothé Pellechia
Publikováno v:
Diagnostic Pathology
Diagnostic Pathology, Vol 7, Iss 1, p 93 (2012)
Diagnostic Pathology, Vol 7, Iss 1, p 93 (2012)
Introduction Hemophilia A is an X linked recessive hemorrhagic disorder caused by mutations in the F8 gene that lead to qualitative and/or quantitative deficiencies of coagulation factor VIII (FVIII). Molecular diagnosis of hemophilia A is challengin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeee28e7047aabd34baca95943d9c301
https://doi.org/10.1186/1746-1596-7-93
https://doi.org/10.1186/1746-1596-7-93
Autor:
Amel Elgaaied Ben Ammar, Wijden Elborji, Emna Gouider, Asma Jlizi, Kaouther Zahra, Rim Sassi, Balkis Meddeb, Moez Zorgan, Hejer Elmahmoudi, Fatma Ben-lakhal
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 92 (2012)
Diagnostic Pathology
Diagnostic Pathology
Inherited factor VII (FVII) deficiency is a rare disorder characterized by a bleeding phenotype varying from mild to severe. To date, more than 200 mutations have been described along the F7 gene encoding for FVII. The aim of this study was the ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edec4d60759709377da378fd57a3b728
http://www.diagnosticpathology.org/content/7/1/92
http://www.diagnosticpathology.org/content/7/1/92