Publications by authors named "Ahlem Amouri"

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Characteristics and outcome of pediatric mixed-phenotype acute leukemia treated with EORTC 58951 protocol: An observational study in Tunisia.
Ameni Yahia, Marwa Bahri, Yosr Ben Abdennebi, Emna Azza, Fatma Ben Lakhel, Ahlem Amouri

Arch Pediatr· April 2025

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Gene Mutations in North African Fanconi Anemia Patients.
Abir Ben Haj Ali, Olfa Messaoud, Sahar Elouej, Faten Talmoudi, Wiem Ayed, Ahlem Amouri

Front Genet· February 2021

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Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro-oculo-facio-skeletal syndrome.
Abir Ben Haj Ali, Ahlem Amouri, Marwa Sayeb, Saloua Makni, Wajih Hammami

Mol Genet Genomic Med· July 2019

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Chromosomal abnormalities in 163 Tunisian couples with recurrent miscarriages.
Wiem Ayed, Islem Messaoudi, Zouhour Belghith, Wajih Hammami, Imen Chemkhi, Ahlem Amouri

Pan Afr Med J· December 2017

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Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia.
Nizar Ben Halim, Sana Hsouna, Khaled Lasram, Insaf Rejeb, Asma Walha, Ahlem Amouri

Am J Hum Biol· December 2016

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Prevalence of Y chromosome microdeletions in infertile Tunisian men.
Wajih Hammami, Olfa Kilani, Mariem Ben Khelifa, Wiem Ayed, Sonia Abdelhak, Ahlem Amouri

Ann Biol Clin (Paris)· May 2016

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Cytogenetic abnormalities in Tunisian women with premature ovarian failure.
Wiem Ayed, Ahlem Amouri, Wajih Hammami, Olfa Kilani, Zinet Turki

C R Biol· December 2014

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Chromosomal evaluation in a group of Tunisian patients with non-obstructive azoospermia and severe oligozoospermia attending a Tunisian cytogenetic department.
Ahlem Amouri, Wajih Hammami, Olfa Kilani, Abderrezzak Bouzouita, Wiem Ayed

C R Biol· April 2014

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High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.
Ahlem Amouri, Faten Talmoudi, Olfa Messaoud, Catherine D d'Enghien, Mariem B Rekaya

Mol Genet Genomic Med· March 2014

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Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in Tunisia.
Faten Talmoudi, Lobna Kammoun, Nizar Benhalim, Lamia Torjemane, Monia Ouederni, Ahlem Amouri

J Pediatr Hematol Oncol· October 2013

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Consanguinity, endogamy, and genetic disorders in Tunisia.
Nizar Ben Halim, Nissaf Ben Alaya Bouafif, Lilia Romdhane, Rym Kefi Ben Atig, Ibtissem Chouchane, Ahlem Amouri

J Community Genet· April 2013

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Differentiation of Fanconi anemia and aplastic anemia using mitomycin C test in Tunisia.
Faten Talmoudi, Olfa Kilani, Wiem Ayed, Nizar Ben Halim, Fethi Mellouli, Ahlem Amouri

C R Biol· January 2013

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A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype-genotype correlation.
Mariem Ben Rekaya, Olfa Messaoud, Amel Mebazaa, Olfa Riahi, Hela Azaiez, Ahlem Amouri

J Genet· December 2011

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Genetic homogeneity of mutational spectrum of group-A xeroderma pigmentosum in Tunisian patients.
Olfa Messaoud, Mariem Ben Rekaya, Wafa Cherif, Faten Talmoudi, Hammouda Boussen, Ahlem Amouri

Int J Dermatol· May 2010

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Identification of a novel mutation in FOXL2 gene that leads to blepharophimosis ptosis epicanthus inversus and telecanthus syndrome in a Tunisian consanguineous family.
Ibtissem Chouchene, Kaouthar Derouiche, Afif Chaabouni, Lamia Cherif, Ahlem Amouri

Genet Test Mol Biomarkers· February 2010

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Single autologous stem-cell transplantation followed by maintenance therapy with thalidomide is superior to double autologous transplantation in multiple myeloma: results of a multicenter randomized clinical trial.
Abderrahman Abdelkefi, Saloua Ladeb, Lamia Torjman, Tarek Ben Othman, Amel Lakhal, Ahlem Amouri

Blood· February 2008

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Cytogenetics and fluorescence in situ hybridization assessment of sex-chromosome mosaicism in Klinefelter's syndrome.
Nouha Bouayed Abdelmoula, Ahlem Amouri, Marie-France Portnoi, Ali Saad, Tahia Boudawara

Ann Genet· October 2005

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Fanconi anemia: contribution of molecular analyses to the identification of bone marrow graft donors and the study of chimerism in grafted patients.
Chiraz Bouchlaka, Tarek Ben Othman, Lamia Aissaoui, Houda Elloumi, Moez Elloumi, Ahlem Amouri

Genet Test· April 2005

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Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.
Chiraz Bouchlaka, Sonia Abdelhak, Ahlem Amouri, Hela Ben Abid, Sondes Hadiji

J Hum Genet· October 2003

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