Works by Ouederni, Monia

Results: 21

Sideroblastic anemia in children: challenges in diagnosis and management in three cases.

Published in:

Annals of Hematology, 2025, v. 104, n. 4, p. 2537, doi. 10.1007/s00277-025-06266-5

By:

Rekaya, Samia;
Ben Fraj, Ilhem;
Hamdi, Rym;
Ben Taieb, Aicha;
Merdassi, Amani;
Jouini, Hamida;
Zarrouk, Hajer;
Zaiter, Ikram;
Kouki, Ridha;
Bejaoui, Mohamed;
Mellouli, Fethi;
Ben Khaled, Monia;
Ouederni, Monia

Publication type:

Article

Feminizing Adrenocortical Adenoma in a 5 Year-old Girl.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2009, v. 22, n. 1, p. 79, doi. 10.1515/JPEM.2009.22.1.79

By:

Bouyahia, Olfa;
Gharsallah, Lamia;
Ouederni, Monia;
Boukthir, Samir;
Mrad, Sonia Mazigh;
Gharbi, Azza Sammoud El

Publication type:

Article

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

Published in:

Frontiers in Immunology, 2023, v. 13, p. 01, doi. 10.3389/fimmu.2022.1057679

By:

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

Publication type:

Article

Incidence and risk factors for osteonecrosis of the femoral head in five hundred and ten sickle cell disease paediatric patients.

Published in:

International Orthopaedics, 2023, v. 47, n. 12, p. 2941, doi. 10.1007/s00264-023-05886-8

By:

Ouederni, Monia;
Rouag, Hatem;
Ben Fraj, Ilhem;
Rekaya, Samia;
Kouki, Ridha;
Lamouchi, Takwa;
Zaiter, Ikram;
Mellouli, Fethi;
Bejaoui, Mohamed;
Ben Khaled, Monia

Publication type:

Article

Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency.

Published in:

Clinical Infectious Diseases, 2014, v. 58, n. 2, p. 204, doi. 10.1093/cid/cit722

By:

Ouederni, Monia;
Sanal, Ozden;
Ikincioğullari, Aydan;
Tezcan, Ilhan;
Dogu, Figen;
Sologuren, Ithaisa;
Pedraza-Sánchez, Sigifredo;
Keser, Melike;
Tanir, Gonul;
Nieuwhof, Chris;
Colino, Elena;
Kumararatne, Dinakantha;
Levy, Jacov;
Kutukculer, Necil;
Aytekin, Caner;
Herrera-Ramos, Estefanía;
Bhatti, Micah;
Karaca, Neslihan;
Barbouche, Ridha;
Broides, Arnon

Publication type:

Article

Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study.

Published in:

Scandinavian Journal of Immunology, 2019, v. 89, n. 6, p. N.PAG, doi. 10.1111/sji.12763

By:

Janssen, Lisanne M. A.;
Hout, Roeland W. N. M.;
de Vries, Esther;
Pignata, Claudio;
Cirillo, Emilia;
Arkwright, Peter D.;
Lougaris, Vassilos;
Buckland, Matthew;
Garcia‐Prat, Marina;
d'Hebron, Vall;
Soler‐Palacin, Pere;
Ouederni, Monia;
Kralickova, Pavlina;
Abolhassani, Hassan;
Hammerstrom, Lennart;
Aghamohamamdi, Asghar;
Santos‐Pérez, Juan L.;
Sobh, Ali;
van de Werff ten Bosch, Jutte;
Henriet, Stefanie

Publication type:

Article

Hypertransaminasemia revealing a clinically silent muscular dystrophy in a child with sickle cell disease.

Published in:

2018

By:

Guirat Dhouib, Naouel;
Khaled, Monia Ben;
Ouederni, Monia;
Besbes, Habib;
Mellouli, Fethi;
Bejaoui, Mohamed

Publication type:

Case Study

Myocardial and liver iron overload, assessed using T2* magnetic resonance imaging with an excel spreadsheet for post processing in Tunisian thalassemia major patients.

Published in:

2017

By:

Ouederni, Monia;
Ben Khaled, Monia;
Mellouli, Fethi;
Mnif, Nejla;
Bejaoui, Mohamed;
Ben Fraj, Elhem;
Dhouib, Nawel;
Yakoub, Ismehen;
Abbes, Selem;
Yakoub, Ismehen Ben

Publication type:

journal article

Consanguineous unions and endogamy in families of beta-thalassaemia patients from two Mediterranean populations: Tunisia and Italy.

Published in:

Annals of Human Biology, 2019, v. 46, n. 7/8, p. 610, doi. 10.1080/03014460.2019.1695936

By:

Weslati, Ramla;
Ouederni, Monia;
Ruffo, Giovanbattista;
Khaled, Monia Ben;
Kouki, Ridha;
Di Girgenti, Caterine;
Borsellino, Zelia;
Sammartano, Irene;
El Gazzah, Mohamed;
El- Bok, Safia;
Bejaoui, Mohamed

Publication type:

Article

Full Genome Characterization of Respiratory Syncytial Virus Causing a Fatal Infection in an Immunocompromised Patient in Tunisia.

Published in:

2022

By:

Curini, Valentina;
Marcacci, Maurilia;
Abid, Salma;
Ouederni, Monia;
ElMoussi, Awatef;
Charaa, Latifa;
Achour, Wafa;
Ouhichi, Ramzi;
Maazaoui, Latifa;
Di Pasquale, Adriano;
ElGhord, Hakim;
Gzara, Ahlem;
Ripani, Alessandro;
Di Giallonardo, Francesca;
Cammà, Cesare;
Lorusso, Alessio;
Boubaker, Ilhem Boutiba-Ben

Publication type:

Case Study

FANCA Gene Mutations in North African Fanconi Anemia Patients.

Published in:

Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.610050

By:

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

Publication type:

Article

Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies.

Published in:

Clinical Pediatrics, 2022, v. 61, n. 9, p. 629, doi. 10.1177/00099228221096329

By:

Mellouli, Fethi;
Ksouri, Habib;
Lajhouri, Maïssa;
Ben Khaled, Monia;
Rekaya, Samia;
Ben Fraj, Elhem;
Ouederni, Monia;
Barbouche, Mohamed Ridha;
Bejaoui, Mohamed

Publication type:

Article

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

Published in:

2021

By:

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

Publication type:

Letter

Successful Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide in a Severe Combined Immune Deficiency Patient: a First Report.

Published in:

2016

By:

Ouederni, Monia;
Mellouli, Fethi;
Khaled, Monia;
Kaabi, Houda;
Picard, Capucine;
Bejaoui, Mohamed

Publication type:

Letter

Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012).

Published in:

Journal of Clinical Immunology, 2015, v. 35, n. 8, p. 745, doi. 10.1007/s10875-015-0206-9

By:

Mellouli, Fethi;
Mustapha, Imen;
Khaled, Monia;
Besbes, Habib;
Ouederni, Monia;
Mekki, Najla;
Ali, Meriem;
Larguèche, Beya;
Hachicha, Mongia;
Sfar, Tahar;
Gueddiche, Neji;
Barsaoui, Siheme;
Sammoud, Azza;
Boussetta, Khadija;
Becher, Saida;
Meherzi, Ahmed;
Guandoura, Najoua;
Boughammoura, Lamia;
Harbi, Abdelaziz;
Amri, Fethi

Publication type:

Article

SARS-CoV-2 excretion and genetic evolution in nasopharyngeal and stool samples from primary immunodeficiency and immunocompetent pediatric patients.

Published in:

Virology Journal, 2025, v. 22, n. 1, p. 1, doi. 10.1186/s12985-025-02628-7

By:

Khemiri, Haifa;
Ben Fraj, Ilhem;
Lorusso, Alessio;
Mekki, Najla;
Mangone, Iolanda;
Gdoura, Mariem;
Di Pasqual, Adriano;
Cammà, Cesare;
Di Lollo, Valeria;
Cherni, Asma;
Touzi, Henda;
Sadraoui, Amel;
Meddeb, Zina;
Hogga, Nahed;
Ben Mustapha, Imen;
Barbouche, Mohamed-Ridha;
Ouederni, Monia;
Triki, Henda;
Haddad-Boubaker, Sondes

Publication type:

Article

Reversion of neurovirulent mutations, recombination and high intra‐host diversity in vaccine‐derived poliovirus excreted by patients with primary immune deficiency.

Published in:

Journal of Medical Virology, 2024, v. 96, n. 9, p. 1, doi. 10.1002/jmv.29918

By:

Ben Salem, Imene;
Khemiri, Haifa;
Drechsel, Oliver;
Arbi, Marwa;
Böttcher, Sindy;
Mekki, Najla;
Ben Fraj, Ilhem;
Souiai, Oussama;
Yahyaoui, Mahrez;
Ben Farhat, Essia;
Meddeb, Zina;
Touzi, Henda;
Ben Mustapha, Imene;
BenKahla, Alia;
Ouederni, Monia;
Barbouche, Mohamed‐R.;
Diedrich, Sabine;
Triki, Henda;
Haddad‐Boubaker, Sondes

Publication type:

Article

Clinical features and predictors of osteoarticular manifestations in common variable immunodeficiency.

Published in:

Clinical Rheumatology, 2023, v. 42, n. 11, p. 3123, doi. 10.1007/s10067-023-06722-5

By:

Ben Khaled, Monia;
Merdassi, Amani;
Rekaya, Samia;
Fraj, Ilhem Ben;
Lamouchi, Takwa;
Zaiter, Ikram;
Kouki, Ridha;
Bejaoui, Mohamed;
Mellouli, Fethi;
Ouederni, Monia

Publication type:

Article

Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.

Published in:

Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2021, v. 55, n. 1, p. 117, doi. 10.33594/000000333

By:

Trabelsi, Nawel;
Bouguerra, Ghada;
Haddad, Faten;
Ouederni, Monia;
Darragi, Imen;
Boudrigua, Imen;
Chaouachi, Dorra;
Barmat, Mbarka;
Fouzai, Chaker;
Bejaoui, Mohamed;
Menif, Samia;
Kraiem, Imen;
Abbes, Salem

Publication type:

Article

Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family.

Published in:

Annals of Clinical Biochemistry, 2023, v. 60, n. 2, p. 81, doi. 10.1177/00045632221134688

By:

Kalai, Miniar;
Moumni, Imen;
Ouragini, Houyem;
Ben Fraj, Ilhem;
Mellouli, Fethi;
Ouederni, Monia;
Chaouachi, Dorra;
Boudriga, Imen;
Menif, Samia

Publication type:

Article

A membranous nephropathy in a 5 year-old boy: and if that's not all? A nephrology quiz.

Published in:

Journal of Nephrology (JNonline), 2024, v. 37, n. 3, p. 821, doi. 10.1007/s40620-023-01821-7

By:

Boussetta, Abir;
Jellouli, Manel;
Hajji, Meriem;
Rekaya, Samia;
Ouederni, Monia;
Abderrahim, Ezzeddine;
Gargah, Tahar

Publication type:

Article