A nine-month-old-boy with Atypical Hemophagocytic Lymphohistiocytosis

por Ouederni, Monia, Ben Khaled, Monia, Rekaya, Samia, Ben Fraj, Ilhem, Mellouli, Fethi, Bejaoui, Mohamed
Publicado 2017

Growth and Endocrine Function in Tunisian Thalassemia Major Patients

por Dhouib, Naouel Guirat, Ben Khaled, Monia, Ouederni, Monia, Besbes, Habib, Kouki, Ridha, Mellouli, Fethi, Bejaoui, Mohamed
Publicado 2018

Successful treatment of fusarium solani ecthyma gangrenosum in a patient affected by leukocyte adhesion deficiency type 1 with granulocytes transfusions

por Mellouli, Fethi, Ksouri, Habib, Barbouche, Ridha, Maamer, Mongi, Hamed, Leila Ben, Hmida, Slama, Hassen, Assia Ben, Béjaoui, Mohamed
Publicado 2010

PB2543: CIRCULATING MICROVESICLES AS POTENTIAL CELLULAR BIOMARKERS FOR THROMBOTIC RISKS IN BETA THALASSEMIA

por Chebbi, Mariem, Khalfaoui, Khouloud, Saidani, Sihem, Safra, Ines, Barmate, Mbarka, Chaouechi, Dorra, Benkhaled, Monia, Ouederni, Monia, Mellouli, Fethi, Menif, Samia, Moumni, Imen
Publicado 2023

Haplotype Map of Sickle Cell Anemia in Tunisia

por Moumni, Imen, Ben Mustapha, Maha, Sassi, Sarra, Zorai, Amine, Ben Mansour, Ikbel, Douzi, Kais, Chouachi, Dorra, Mellouli, Fethi, Bejaoui, Mohamed, Abbes, Salem
Publicado 2014

Cutaneous Manifestations of Primary Immunodeficiency Diseases in Tunisian Children

por Dhouib, Naouel Guirat, Ben Khaled, Monia, Ouederni, Monia, Ben-Mustapha, Imen, Kouki, Ridha, Besbes, Habib, Barbouche, Mohamed Ridha, Mellouli, Fethi, Bejaoui, Mohamed
Publicado 2018

Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome)

por Guirat-Dhouib, Naouel, Baccar, Yemen, Mustapha, Imène Ben, ouederni, Monia, Chouaibi, Sameh, El Fekih, Nadia, Barbouche, Mohamed Ridha, Fezaa, Bassima, Kouki, Ridha, Hmida, Slama, Mellouli, Fethi, Bejaoui, Mohamed
Publicado 2012

FANCA Gene Mutations in North African Fanconi Anemia Patients

por Ben Haj Ali, Abir, Messaoud, Olfa, Elouej, Sahar, Talmoudi, Faten, Ayed, Wiem, Mellouli, Fethi, Ouederni, Monia, Hadiji, Sondes, De Sandre-Giovannoli, Annachiara, Delague, Valérie, Lévy, Nicolas, Bogliolo, Massimo, Surrallés, Jordi, Abdelhak, Sonia, Amouri, Ahlem
Publicado 2021

Containment of Local COVID-19 Outbreak Among Hematopoietic Stem Cell Transplant Recipients and Healthcare Workers in a Pediatric Stem Cell Unit

por Ouederni, Monia, Rekaya, Samia, Bouabdallah, Oussema, Ben Fradj, Ilhem, Kouki, Ridha, Chebbi, Yosr, Ammar, Sahar Ben, Lamouchi, Takwa, Lachiheb, Asma, Zekri, Nessrine, Laajili, Siwar, Zaiter, Ikram, Hamzaoui, Agnes, Bejaoui, Mohamed, Mellouli, Fethi, Achour, Wafa, Ben Khaled, Monia
Publicado 2021

Diagnostic challenge in a series of eleven patients with hyper IgE syndromes

por Yaakoubi, Roukaya, Mekki, Najla, Ben-Mustapha, Imen, Ben-Khemis, Leila, Bouaziz, Asma, Ben Fraj, Ilhem, Ammar, Jamel, Hamzaoui, Agnès, Turki, Hamida, Boussofara, Lobna, Denguezli, Mohamed, Haddad, Samir, Ouederni, Monia, Bejaoui, Mohamed, Chan, Koon Wing, Lau, Yu Lung, Mellouli, Fethi, Barbouche, Mohamed-Ridha, Ben-Ali, Meriem
Publicado 2023

High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis

por Amouri, Ahlem, Talmoudi, Faten, Messaoud, Olfa, d'Enghien, Catherine D, Rekaya, Mariem B, Allegui, Ines, Azaiez, Héla, Kefi, Rym, Abdelhak, Ahlem, Meseddi, Sondes H, Torjemane, Lamia, Ouederni, Monia, Mellouli, Fethi, Abid, Héla B, Aissaoui, Lamia, Bejaoui, Mohamed, Othmen, Tarek B, Lyonnet, Dominique S, Soulier, Jean, Hachicha, Mongia, Dellagi, Koussay, Abdelhak, Sonia, Fanconi, Tunisian
Publicado 2014