Publications by authors named "Faten Kallel"

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Atypical acquired hemophilia linked with primary biliary cholangitis: a unique case presentation.
Fatma Megdiche, Nour Siala, Faten Kallel, Imen Krichen, Hend Hachicha, Naourez Kallel, Choumous Kallel

Future Sci OA· December 2025

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Primary Cutaneous NK/T-Cell Lymphoma With Aberrant CD20 Expression Responsive to SMILE Chemotherapy.
Malek Cherif, Ikram Gassara, Nour Siala, Rim Chaabouni, Khadija Sellami, Faten Kallel

J Cutan Pathol· November 2025

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Characterization of novel mutations in the TEL-patch domain of the telomeric factor TPP1 associated with telomere biology disorders.
Alexis Bertrand, Ibrahima Ba, Laëtitia Kermasson, Vithura Pirabakaran, Noémie Chable, Faten Kallel

Hum Mol Genet· March 2024

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Biclonal Gammopathies in South Tunisia: Clinical and Biological Characteristics.
Ameni Jerbi, Hend Hachicha, Aida Charfi, Faten Kallel, Sawsan Feki

Lab Med· September 2023

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Complexity of diagnosing and treating langerhans cell sarcoma: A case report.
Maha Charfi, Maissa Lajnaf, Faten Kallel, Ines Saguem, Olfa Kassar

Tunis Med· July 2023

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Non-Hodgkin's lymphoma developed during imatinib mesylate treatment of chronic myeloid leukemia.
Olfa Kassar, Aicha Ben Kahla, Asma Koubaa, Faten Kallel, Imen Ben Amor

J Oncol Pharm Pract· June 2023

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Hemophilia in the south of Tunisia.
Olfa Kassar, Maha Charfi, Fatma Megdiche, Yosra Fakhfakh, Faten Kallel

Blood Coagul Fibrinolysis· October 2022

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Aplastic anemia secondary to tyrosine kinase inhibitor therapy in a patient with chronic myeloid leukemia.
Olfa Kassar, Rahma Mallek, Fatma Ben Said, Faten Kallel, Kamilia Ksouda

J Oncol Pharm Pract· March 2022

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Prospective observational study of palliative care in hematological malignancies: Report of one year of practice.
Faten Kallel, Sonda Masmoudi, Olfa Kassar, Rahma Mallek, Moez Medhaffar

Transfus Clin Biol· February 2022

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Hypersensitivity pneumonitis related to imatinib mesylate therapy in a patient with chronic myeloid leukemia.
Faten Kallel, Olfa Kassar, Imen Maaloul, Maha Charfi, Kamilia Ksouda

J Oncol Pharm Pract· October 2021

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Homozygous pArg610del Mutation Unusually Associated With Severe Delay of Growth in 2 Acid Sphingomyelinase Deficiency-affected Sibs.
Manel Naifar, Faten Kallel, Faten HadjKacem, Hela Boudabous, Rim Kallel

J Pediatr Hematol Oncol· August 2020

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[Gaucher disease type 1 in late onset].
Sondes Mseddi, Faten Kallel, Ines Jedidi, Faten Ben Rhouma, Olfa Kassar, Choumous Kallel

Tunis Med· October 2012

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Adult Gaucher disease in southern Tunisia: report of three cases.
Faten Ben Rhouma, Faten Kallel, Rym Kefi, Wafa Cherif, Majdi Nagara

Diagn Pathol· January 2012

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Haematological and cytogenetic responses after only 7 days of Lenalidomide in a patient with myelodysplastic syndrome and chromosome 5q deletion.
Sondes Hadiji Mseddi, Faten Kallel, Olfa Kassar, Moez Elloumi, Ines Jedidi

Leuk Res· September 2011

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