Works by Mellouli, Fethi

Results: 29

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

Generalized allergy due to zinc in insulin treated with zinc-free insulin.

Published in:

Acta Diabetologica, 2012, v. 49, n. 3, p. 239, doi. 10.1007/s00592-010-0230-4

By:

Ben Ammar, Ines;
Ksouri, Habib;
Trabelsi, Nabil;
Mellouli, Fethi;
Ben Mami, Faïka;
Dakhli, Saber;
Achour, Ahmed

Publication type:

Article

Autoimmune Polyglandular Syndrome Type II After Bone Marrow Transplant: Real Transfer or Acceleration of a Programmed Disease?

Published in:

Experimental & Clinical Transplantation, 2012, v. 10, n. 1, p. 76, doi. 10.6002/ect.2011.0062

By:

Mellouli, Fethi;
Ksouri, Habib;
Lakhal, Amel;
Torjmen, Lamia;
Ladeb, Saloua;
Othman, Tarek Ben;
Hmida, Slama;
Béjaoui, Mohamed

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

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

Revisiting beta thalassemia intermedia: past, present, and future prospects.

Published in:

Hematology, 2017, v. 22, n. 10, p. 607, doi. 10.1080/10245332.2017.1333246

By:

Ben Salah, Naouel;
Bou-Fakhredin, Rayan;
Mellouli, Fethi;
Taher, Ali T.

Publication type:

Article

The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients.

Published in:

Hematology, 2017, v. 22, n. 3, p. 178, doi. 10.1080/10245332.2016.1253253

By:

Kalai, Miniar;
Dridi, Marwa;
Chaouch, Leila;
Moumni, Imen;
Ouragini, Houyem;
Darragi, Imen;
Boudrigua, Imen;
Chaouachi, Dorra;
Mellouli, Fethi;
Bejaoui, Mohamed;
Abbes, Salem

Publication type:

Article

Phenotypic and molecular genetic analysis of Pyruvate Kinase deficiency in a Tunisian family.

Published in:

Egyptian Journal of Medical Human Genetics, 2016, v. 17, n. 3, p. 265, doi. 10.1016/j.ejmhg.2015.09.001

By:

Mouna, Jaouani;
Nadia, Hamdi;
Leila, Chaouch;
Miniar, Kalai;
Fethi, Mellouli;
Imen, Darragi;
Imen, Boudriga;
Dorra, Chaouachi;
Mohamed, Bejaoui;
Salem, Abbes

Publication type:

Article

Primary immunodeficiencies in highly consanguineous North African populations.

Published in:

Annals of the New York Academy of Sciences, 2011, v. 1238, n. 1, p. 42, doi. 10.1111/j.1749-6632.2011.06260.x

By:

Barbouche, Mohamed‐Ridha;
Galal, Nermeen;
Ben‐Mustapha, Imen;
Jeddane, Leïla;
Mellouli, Fethi;
Ailal, Fatima;
Bejaoui, Mohamed;
Boutros, Jeanette;
Marsafy, Aisha;
Bousfiha, Ahmed Aziz

Publication type:

Article

Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.

Published in:

Immunogenetics, 2016, v. 68, n. 1, p. 19, doi. 10.1007/s00251-015-0878-6

By:

Ouadani, Hanen;
Ben-Mustapha, Imen;
Ben-ali, Meriem;
Ben-khemis, Leila;
Larguèche, Beya;
Boussoffara, Raoudha;
Maalej, Sonia;
Fetni, Ilhem;
Hassayoun, Saida;
Mahfoudh, Abdelmajid;
Mellouli, Fethi;
Yalaoui, Sadok;
Masmoudi, Hatem;
Bejaoui, Mohamed;
Barbouche, Mohamed-Ridha

Publication type:

Article

Contribution to the Description of the β-Thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity.

Published in:

Hemoglobin, 2004, v. 28, n. 3, p. 189, doi. 10.1081/HEM-120040305

By:

Chouk, Imen;
Daoud, Béchir Ben;
Mellouli, Fethi;
Bejaoui, Mohamed;
Gérard, Nathalie;
Dellagi, Koussay;
Abbes, Salem

Publication type:

Article

Restriction mapping of β<sup>S</sup> locus among tunisian sickle-cell patients.

Published in:

American Journal of Human Biology, 2011, v. 23, n. 6, p. 815, doi. 10.1002/ajhb.21224

By:

Imen, Moumni;
Ikbel, Ben Mansour Mosbehi;
Leila, Chaouch;
Fethi, Mellouli;
Amine, Zorai;
Mohamed, Bejaoui;
Salem, Abbes

Publication type:

Article

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

Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families.

Published in:

Journal of Clinical Immunology, 2020, v. 40, n. 1, p. 96, doi. 10.1007/s10875-019-00706-4

By:

Ben-Ali, Meriem;
Kechout, Nadia;
Mekki, Najla;
Yang, Jing;
Chan, Koon Wing;
Barakat, Abdelhamid;
Aadam, Zahra;
Gamara, Jouda;
Gargouri, Lamia;
Largueche, Beya;
BelHadj-Hmida, Nabil;
Nedri, Amel;
Ameur, Houcine Ben;
Mellouli, Fethi;
Boukari, Rachida;
Bejaoui, Mohamed;
Bousfiha, Aziz;
Ben-Mustapha, Imen;
Lau, Yu-Lung;
Barbouche, Mohamed-Ridha

Publication type:

Article

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

Clinical, Immunological and Genetic Findings of a Large Tunisian Series of Major Histocompatibility Complex Class II Deficiency Patients.

Published in:

Journal of Clinical Immunology, 2013, v. 33, n. 4, p. 865, doi. 10.1007/s10875-013-9863-8

By:

Ben-Mustapha, Imen;
Ben-Farhat, Khaoula;
Guirat-Dhouib, Naouel;
Dhemaied, Emna;
Larguèche, Beya;
Ben-Ali, Meriem;
Chemli, Jalel;
Bouguila, Jihène;
Ben-Mansour, Lamia;
Mellouli, Fethi;
Khemiri, Monia;
Béjaoui, Mohamed;
Barbouche, Mohamed-Ridha

Publication type:

Article

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

Published in:

BMC Dermatology, 2010, v. 10, p. 10, doi. 10.1186/1471-5945-10-10

By:

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

Publication type:

Article

Kaposi's sarcoma in a child with Wiskott-Aldrich syndrome.

Published in:

2006

By:

Picard, Capucine;
Mellouli, Fethi;
Duprez, Renan;
Chédeville, Gaëlle;
Neven, Bénédicte;
Fraitag, Sylvie;
Delaunay, Jean;
Le Deist, Françoise;
Fischer, Alain;
Blanche, Stéphane;
Bodemer, Christine;
Gessain, Antoine;
Casanova, Jean-Laurent;
Bejaoui, Mohamed;
Chédeville, Gaëlle;
Neven, Bénédicte;
Le Deist, Françoise;
Blanche, Stéphane

Publication type:

journal article

Effectiveness of fixed 50% nitrous oxide oxygen mixture and EMLA cream for insertion of central venous catheters in children.

Published in:

Pediatric Blood & Cancer, 2004, v. 43, n. 7, p. 777, doi. 10.1002/pbc.20186

By:

Abdelkefi, Abderrahman;
Abdennebi, Yosr Ben;
Mellouli, Fethi;
Othman, Tarek Ben;
Torjman, Lamia;
Ladeb, Saloua;
Aouf, Sami;
Béjaoui, Mohamed;
Abdeladhim, Abdeladhim Ben

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

Possible transfer of vitiligo by allogeneic bone marrow transplantation: A case report.

Published in:

Pediatric Transplantation, 2009, v. 13, n. 8, p. 1058, doi. 10.1111/j.1399-3046.2008.01093.x

By:

Mellouli, Fethi;
Ksouri, Habib;
Dhouib, Nawel;
Torjmen, Lamia;
Abdelkefi, Abderrahman;
Ladeb, Saloua;
Othman, Tarek Ben;
Hmida, Slama;
Hassen, Assia Ben;
Béjaoui, Mohamed

Publication type:

Article

Transmission of type 1 diabetes by bone marrow transplantation: A case report.

Published in:

Pediatric Transplantation, 2009, v. 13, n. 1, p. 119, doi. 10.1111/j.1399-3046.2007.00889.x

By:

Mellouli, Fethi;
Ksouri, Habib;
Torjmen, Lamia;
Abdelkefi, Abderrahman;
Ladeb, Saloua;
Othman, Tarek Ben;
Hassen, Assia Ben;
Béjaoui, Mohamed

Publication type:

Article

Bone marrow transplantation without conditioning regimen in Omenn syndrome: A case report.

Published in:

Pediatric Transplantation, 2007, v. 11, n. 8, p. 922, doi. 10.1111/j.1399-3046.2007.00787.x

By:

Mellouli, Fethi;
Torjmen, Lamia;
Ksouri, Habib;
Abdelkefi, Abdelrahmen;
Ladab, Saloua;
Barbouche, Ridha;
Othman, Tarek Ben;
Hassen, Assia Ben;
Bejaoui, Mohamed

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