Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Samira Aggoune"'
Autor:
Azzeddine Tahiat, Reda Belbouab, Abdelghani Yagoubi, Saliha Hakem, Faiza Fernini, Malika Keddari, Hayet Belhadj, Souad Touri, Samira Aggoune, Jennifer Stoddard, Julie Niemela, Farida Zerifi, Souhila Melzi, Rawda Aboura, Amina Saad-Djaballah, Yacine Ferhani, Abdalbasset Ketfi, Hassen Messaoudi, Tahar Bencharif Madani, Zouleikha Benhacine, Abdelhak Dehimi, Kamelia Okka, Fairouz Amroune, Meriem Fellahi, Chafa Bendahmane, Radia Khoulani, Asma Oukil, Asma Soufane, Imene Bourelaf, Chahynez Boubidi, Nadia Boukhenfouf, Mohamed Amine Ifri, Noureddine Khelafi, Houda Boudiaf, Tahar Khelifi Touhami, Fethi Meçabih, Malika Boucelma, Amara Zelaci, Ourida Gacem, Mohamed Samir Ladj, Azzedine Mekki, Nadia Bensaadi, Malika Benhalima, Zoulikha Zeroual, Belkacem Bioud, Mustapha Benameur, Rachid Bouhdjila, Zahir Bouzerar, Ouardia Ibsaine, Hachemi Maouche, Leila Kedji, Leila Smati, Rachida Boukari, Claude Lambert, Sergio D. Rosenzweig, Luigi D. Notarangelo, Kamel Djenouhat
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
PurposeIn this study, we retrospectively reviewed the use of flow cytometry (FCM) in the diagnosis of inborn errors of immunity (IEIs) at a single center in Algeria. Sharing insights into our practical experience, we present FCM based diagnostic appr
Externí odkaz:
https://doaj.org/article/0373dc062c034461aab9cf65179e134c
Publikováno v:
European Medical Journal Hematology, Pp 53-57 (2022)
Von Willebrand disease (VWD) is a bleeding disorder, resulting from a quantitative or qualitative defect in von Willebrand factor (VWF). A regulatory role for VWF in angiogenesis was postulated upon the clinical observation that qualitative or quanti
Externí odkaz:
https://doaj.org/article/d8b4c4f536664829a6e4745285ee1aaa
Autor:
Brahim Belaid, Lydia Lamara Mahammed, Ouardia Drali, Aida Mohand Oussaid, Nabila Souad Touri, Souhila Melzi, Abdelhak Dehimi, Lylia Meriem Berkani, Fatma Merah, Zineb Larab, Ines Allam, Ouarda Khemici, Sonya Yasmine Kirane, Mounia Boutaba, Reda Belbouab, Hadjira Bekkakcha, Assia Guedouar, Abdelhakim Chelali, Brahim Baamara, Djamila Noui, Hadda Baaziz, Radia Rezak, Sidi Mohamed Azzouz, Malika Aichaoui, Assia Moktefi, Redha Mohamed Benhatchi, Meriem Oussalah, Naila Benaissa, Amel Laredj, Assia Bouchetara, Abdelkader Adria, Brahim Habireche, Noureddine Tounsi, Fella Dahmoun, Rabah Touati, Hamza Boucenna, Fadila Bouferoua, Lynda Sekfali, Nadjet Bouhafs, Rawda Aboura, Sakina Kherra, Yacine Inouri, Saadeddine Dib, Nawel Medouri, Noureddine Khelfaoui, Aicha Redjedal, Amara Zelaci, Samah Yahiaoui, Sihem Medjadj, Tahar Khelifi Touhami, Ahmed Kadi, Fouzia Amireche, Imane Frada, Shahrazed Houasnia, Karima Benarab, Chahynez Boubidi, Yacine Ferhani, Hayet Benalioua, Samia Sokhal, Nadia Benamar, Samira Aggoune, Karima Hadji, Asma Bellouti, Hakim Rahmoune, Nada Boutrid, kamelia Okka, Assia Ammour, Houssem Saadoune, Malika Amroun, Hayet Belhadj, Amina Ghanem, Hanane Abbaz, Sana Boudrioua, Besma Zebiche, Assia Ayad, Zahra Hamadache, Nassima Ouaras, Nassima Achour, Nadira Bouchair, Houda Boudiaf, Dahila Bekkat-Berkani, Hachemi Maouche, Zahir Bouzrar, Lynda Aissat, Ouardia Ibsaine, Belkacem Bioud, Leila Kedji, Djazia Dahlouk, Manoubia Bensmina, Abdelkarim Radoui, Mimouna Bessahraoui, Nadia Bensaadi, Azzeddine Mekki, Zoulikha Zeroual, Koon-Wing Chan, Daniel Leung, Amar Tebaibia, Soraya Ayoub, Dalila Mekideche, Merzak Gharnaout, Jean Laurent Casanova, Anne Puel, Yu Lung Lau, Nacira Cherif, Samir Ladj, Leila Smati, Rachida Boukari, Nafissa Benhalla, Reda Djidjik
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundInborn errors of immunity (IEI) predispose patients to various infectious and non-infectious complications. Thanks to the development and expanding use of flow cytometry and increased awareness, the diagnostic rate of IEI has markedly incre
Externí odkaz:
https://doaj.org/article/bf13ba829e374da89147bcc53c874c74
Autor:
Azzeddine Tahiat, Abdelghani Yagoubi, Mohamed Samir Ladj, Reda Belbouab, Samira Aggoune, Laziz Atek, Djamila Bouziane, Souhila Melzi, Chahinez Boubidi, Warda Drali, Chafa Bendahmane, Hamza Iguerguesdaoune, Sihem Taguemount, Asma Soufane, Asma Oukil, Abdalbasset Ketfi, Hassen Messaoudi, Nadia Boukhenfouf, Mohamed Amine Ifri, Tahar Bencharif Madani, Hayet Belhadj, Keltoum Nafissa Benhala, Mokhtar Khiari, Nacera Cherif, Leila Smati, Zakia Arada, Zoulikha Zeroual, Zair Bouzerar, Ouardia Ibsaine, Hachemi Maouche, Rachida Boukari, Kamel Djenouhat
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
ObjectivesTo evaluate the diagnostic and predictive contribution of autoantibodies screening in patients with primary immunodeficiencies (PIDs).MethodsIn the present study, PID patients and healthy controls have been screened for 54 different autoant
Externí odkaz:
https://doaj.org/article/a8b4819826794e1c87e5e2c073de0750
Autor:
Despina Moshous, Jean Donadieu, Samir Benmamar, Hachemi Maouche, Capucine Picard, Feriel Mekimene, Geneviève de Saint Basile, Guy Leverger, Linda Chikhi, Samira Aggoune
Publikováno v:
GMJ Medicine. :95-98
Autor:
Zoulikha Zeroual, Ouardia Ibsaine, Nadia Boukhenfouf, Chafa Bendahmane, Rachida Boukari, Djamila Bouziane, Hassen Messaoudi, Leila Smati, Reda Belbouab, Hamza Iguerguesdaoune, Mokhtar Khiari, Mohamed Samir Ladj, Kamel Djenouhat, Hachemi Maouche, Zakia Arada, Asma Soufane, Abdelghani Yagoubi, Hayet Belhadj, Abdalbasset Ketfi, Zair Bouzerar, Laziz Atek, Sihem Taguemount, Chahinez Boubidi, Azzeddine Tahiat, Samira Aggoune, Warda Drali, Asma Oukil, Souhila Melzi, Nacera Cherif, Mohamed Amine Ifri, Tahar Bencharif Madani, Keltoum Nafissa Benhala
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology, Vol 12 (2021)
ObjectivesTo evaluate the diagnostic and predictive contribution of autoantibodies screening in patients with primary immunodeficiencies (PIDs).MethodsIn the present study, PID patients and healthy controls have been screened for 54 different autoant
Autor:
Samira Aggoune
Publikováno v:
Journal of Medical Science And clinical Research.
Autor:
Houda Hamdi-Rozé, Martine Ropert, Gilles Pelletier, Véronique David, Samira Aggoune, Yves Deugnier, Dominique Simon, Zeineb Ben Ali, Edouard Bardou-Jacquet, Lénaïck Détivaud
Publikováno v:
Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, 2019, 74, pp.30-33. ⟨10.1016/j.bcmd.2018.10.006⟩
Blood Cells, Molecules and Diseases, Elsevier, 2019, 74, pp.30-33. ⟨10.1016/j.bcmd.2018.10.006⟩
Blood Cells, Molecules and Diseases, 2019, 74, pp.30-33. ⟨10.1016/j.bcmd.2018.10.006⟩
Blood Cells, Molecules and Diseases, Elsevier, 2019, 74, pp.30-33. ⟨10.1016/j.bcmd.2018.10.006⟩
International audience; Juvenile hemochromatosis is a rare autosomal recessive disease due to variants in the Hemojuvelin (HJV) gene. Although biological features mimic HFE hemochromatosis, clinical presentation is worst with massive iron overload di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e56349c7715ab480276481cf2961f452
https://univ-rennes.hal.science/hal-01950953
https://univ-rennes.hal.science/hal-01950953