Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Monia Ben Khaled"'
Autor:
Chloé Arfeuille, Yoann Vial, Margaux Cadenet, Aurélie Caye-Eude, Odile Fenneteau, Quentin Neven, Adeline A Bonnard, Simone Pizzi, Giovanna Carpentieri, Yline Capri, Katia Girardi, Lucia Pedace, Marina Macchiaiolo, Kamel Boudhar, Monia ben Khaled, Wadih Abou Chahla, Anne Lutun, Mony Fahd, Séverine Drunat, Elisabetta Flex, Jean-Hugues Dalle, Marion Strullu, Franco Locatelli, Marco Tartaglia, Hélène Cavé
Publikováno v:
Haematologica, Vol 999, Iss 1 (2023)
Juvenile myelomonocytic leukemia (JMML) is a rare, generally aggressive myeloproliferative neoplasm affecting young children. It is characterized by granulomonocytic expansion, with monocytosis infiltrating peripheral tissues. JMML is initiated by mu
Externí odkaz:
https://doaj.org/article/65e8c5154d52490e9ade2007b367450e
Autor:
Afef Rais, Najla Mekki, Faten Fedhila, Mohammed Faraj Alosaimi, Monia Ben Khaled, Amal Zameli, Nourhen Agrebi, Maryam Kallel Sellami, Raif Geha, Imen Ben-Mustapha, Mohamed-Ridha Barbouche
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
ALPS and IPEX are two well-characterized inborn errors of immunity with immune dysregulation, considered as two master models of monogenic auto-immune diseases. Thus, with autoimmunity as their primary clinical manifestation, these two entities may s
Externí odkaz:
https://doaj.org/article/664e8934cd7247bc83644a65edaf2965
Autor:
Ramla Weslati, Monia Ouederni, Giovanbattista Ruffo, Monia Ben Khaled, Ridha Kouki, Caterine Di Girgenti, Zelia Borsellino, Irene Sammartano, Mohamed El Gazzah, Safia El- Bok, Mohamed Bejaoui
Publikováno v:
Annals of Human Biology, Vol 46, Iss 7-8, Pp 610-615 (2019)
Background: Consanguinity increases the incidence of recessive diseases such as beta-thalassaemia major (βTM), one of the most prevalent lethal inherited diseases in the world. Aim: This study aims to identify the frequency of endogamy and consangui
Externí odkaz:
https://doaj.org/article/82e3f339ac2a4e67b2778ba40b6fbd67
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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94827b44f2ed0eba6ef9ddcaa96848e2
https://doi.org/10.1177/00099228221096329
https://doi.org/10.1177/00099228221096329
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d56c878738109eae1e0ef55ecc6db8f
https://doi.org/10.1007/s10875-021-01094-4
https://doi.org/10.1007/s10875-021-01094-4
Autor:
Houyem Ouragini, Sonia Nouira, Emna Bouatrous, Monia Ouederni, Salem Abbes, Samia Menif, Monia Ben Khaled
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:e1055-e1058
Several causes are known to be at the origin of neonatal cyanosis among them methemoglobinemia is by inheritance of an hemoglobin (Hb) M variant. This is a rare condition never been reported in Tunisia so far. Here, we report a Tunisian newborn with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::986b0846d5d4ac9463664d9aa7922296
https://doi.org/10.1097/mph.0000000000002096
https://doi.org/10.1097/mph.0000000000002096
Autor:
Mohamed Bejaoui, Ramla Weslati, Monia Ben Khaled, Ridha Kouki, Monia Ouederni, Giovanbattista Ruffo, Safia El-Bok, Caterine Di Girgenti, Zelia Borsellino, Mohamed El Gazzah, Irene Sammartano
Publikováno v:
Annals of human biology. 46(7-8)
Background: Consanguinity increases the incidence of recessive diseases such as beta-thalassaemia major (βTM), one of the most prevalent lethal inherited diseases in the world.Aim: This study aims ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ee9a39f78b9a4386a132e7f08c5eb0f
https://pubmed.ncbi.nlm.nih.gov/31793346
https://pubmed.ncbi.nlm.nih.gov/31793346
Autor:
Monia Ben Khaled, Ilhem Ben Fraj, N. Dhouib, Ridha Kouki, Mohamed Bejaoui, Fethi Mellouli, Samia Rekaya, Monia Ouederni, Yosra Mankai
Publikováno v:
Blood cells, moleculesdiseases. 80
This study was aimed to identify the predictors of splenic sequestration crisis (SSC) among pediatric patients with sickle cell disease (SCD). This prognosis study was carried out in the pediatric immuno-hematology unit, over 20 years (1998 to 2017),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::234e3e53bc9bb7220a16fc2918d73753
https://pubmed.ncbi.nlm.nih.gov/31670184
https://pubmed.ncbi.nlm.nih.gov/31670184