Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Fethi Mellouli"'
Autor:
Mariem Chebbi, Khouloud Khalfaoui, Sihem Saidani, Ines Safra, Mbarka Barmate, Dorra Chaouechi, Monia Benkhaled, Monia Ouederni, Fethi Mellouli, Samia Menif, Imen Moumni
Publikováno v:
HemaSphere, Vol 7, p e0427349 (2023)
Externí odkaz:
https://doaj.org/article/6063017cd2164706a56ace3703ba4724
Autor:
Roukaya Yaakoubi, Najla Mekki, Imen Ben-Mustapha, Leila Ben-Khemis, Asma Bouaziz, Ilhem Ben Fraj, Jamel Ammar, Agnès Hamzaoui, Hamida Turki, Lobna Boussofara, Mohamed Denguezli, Samir Haddad, Monia Ouederni, Mohamed Bejaoui, Koon Wing Chan, Yu Lung Lau, Fethi Mellouli, Mohamed-Ridha Barbouche, Meriem Ben-Ali
Publikováno v:
Frontiers in Immunology, Vol 13 (2023)
Hyper IgE syndromes (HIES) is a heterogeneous group of Inborn Errors of Immunity characterized by eczema, recurrent skin and lung infections associated with eosinophilia and elevated IgE levels. Autosomal dominant HIES caused by loss of function muta
Externí odkaz:
https://doaj.org/article/83b09f03da244315b6f98c74026a3c85
Autor:
Abir Ben Haj Ali, Olfa Messaoud, Sahar Elouej, Faten Talmoudi, Wiem Ayed, Fethi Mellouli, Monia Ouederni, Sondes Hadiji, Annachiara De Sandre-Giovannoli, Valérie Delague, Nicolas Lévy, Massimo Bogliolo, Jordi Surrallés, Sonia Abdelhak, Ahlem Amouri
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Populations in North Africa (NA) are characterized by a high rate of consanguinity. Consequently, the proportion of founder mutations might be higher than expected and could be a major cause for the high prevalence of recessive genetic disorders like
Externí odkaz:
https://doaj.org/article/bb022a4210ca418a9084d7233c286fe8
Autor:
Naouel GUIRAT, Monia Ben Khaled, Monia Ouederni, Imen Ben-Mustapha, Ridha Kouki, Habib Besbes, Mohamed Ridha Barbouche, Fethi Mellouli, mohamed bejaoui
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 10, Pp e2018065-e2018065 (2018)
Abstract. Skin manifestations are frequent among patients with primary immunodeficiency diseases (PIDs). Their prevalence varies according to the type of immunodeficiency. This review provides the reader with an up-to-date summary of the common derma
Externí odkaz:
https://doaj.org/article/e6032afdbe4349cda64018dd454978af
Autor:
Monia Ouederni, MONIA BEN KHALED, Samia Rekaya, Ilhem Ben Fraj, Fethi Mellouli, Mohamed Bejaoui
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 9, Iss 1, Pp e2017057-e2017057 (2017)
Hemophagocytic lymphohistiocytosis is a life-threatening hyperinflammation caused by uncontrolled proliferation of activated lymphocytes and histiocytes. Often, Hemophagocytic lymphohistiocytosis is an acquired syndrome. We report a case of a 9 month
Externí odkaz:
https://doaj.org/article/dd7cfcb6b74841f982a35d6fb5fcc85f
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
Autor:
Fethi Mellouli, Habib Ksouri, Maïssa Lajhouri, Monia Ben Khaled, Samia Rekaya, Elhem Ben Fraj, Monia Ouederni, Mohamed Ridha Barbouche, Mohamed Bejaoui
Publikováno v:
Clinical Pediatrics. 61:629-644
Chronic granulomatous disease (CGD) is an inherited autosomal recessive or X-Linked primitive immunodeficiency (PID), due to a defective nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex impairing anti-infectious and anti-inflammato
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:
Ikram Zaiter, Agnes Hamzaoui, Sahar Ben Ammar, Yosr Chebbi, Ilhem Ben Fradj, Wafa Achour, Nessrine Zekri, Oussema Bouabdallah, Fethi Mellouli, Asma Lachiheb, Takwa Lamouchi, Monia Ouederni, Ridha Kouki, Mohamed Bejaoui, Siwar Laajili, Monia Ben Khaled, Samia Rekaya
Publikováno v:
Journal of Clinical Immunology
Autor:
Yu-Lung Lau, Najla Mekki, Lamia Gargouri, Imen Ben-Mustapha, Rachida Boukari, Abdelhamid Barakat, Mohamed Bejaoui, Zahra Aadam, Jouda Gamara, Koon Wing Chan, Nabil BelHadj-Hmida, Aziz Bousfiha, Beya Larguèche, Houcine Ben Ameur, Jing Yang, Fethi Mellouli, Amel Nedri, Nadia Kechout, Mohamed-Ridha Barbouche, Meriem Ben-Ali
Publikováno v:
Journal of Clinical Immunology. 40:96-104
Autosomal recessive agammaglobulinemia (ARA) is a primary immunodeficiency characterized by absent peripheral B cells, severe hypogammaglobulinemia, and absent BTK gene mutations. In ARA, mutations occur in genes encoding the pre-B cell receptor (pre