Characterisation of the Paenarthrobacter nicotinovorans ATCC 49919 genome and identification of several strains harbouring a highly syntenic nic-genes cluster
El-Sabeh, Amada, Mlesnita, Andreea-Mihaela, Munteanu, Iustin-Tiberius, Honceriu, Iasmina, Kallabi, Fakhri, Boiangiu, Razvan-Stefan, Mihasan, Marius
Published in BMC genomics (11.09.2023)
Published in BMC genomics (11.09.2023)
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Neurological Characteristics of Allgrove Syndrome: A Case Series
Salah, Dhoha Ben, Elleuch, Mouna, Trimeche, Oumeyma, Zargni, Asma, Kallabi, Fakhri, Sakka, Salma, Mnif, Fatma, Rekik, Nabila, Charfi, Nadia, Kamoun, Hassen, Feki, Mouna Mnif, Kacem, Faten Hadj, Abid, Mohamed
Published in Annals of child neurology (01.04.2024)
Published in Annals of child neurology (01.04.2024)
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Splicing defects in ABCD1 gene leading to both exon skipping and partial intron retention in X-linked adrenoleukodystrophy Tunisian patient
Kallabi, Fakhri, Hadj Salem, Ikhlass, Ben Chehida, Amel, Ben Salah, Ghada, Ben Turkia, Hadhami, Tebib, Neji, Keskes, Leila, Kamoun, Hassen
Published in Neuroscience research (01.08.2015)
Published in Neuroscience research (01.08.2015)
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Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian population
Ben Rhouma, Bochra, Kley, Manuel, Kallabi, Fakhri, Kacem, Faten Hadj, Kammoun, Thouraya, Safi, Wajdi, Keskes, Leila, Mnif, Mouna, Odermatt, Alex, Belguith, Neila
Published in The Journal of steroid biochemistry and molecular biology (01.03.2023)
Published in The Journal of steroid biochemistry and molecular biology (01.03.2023)
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Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low‐GGT intrahepatic cholestasis: Genetic diagnosis and genotype–phenotype correlation assessment
Khabou, Boudour, Kallabi, Fakhri, Abdelaziz, Rim Ben, Maaloul, Ines, Aloulou, Hajer, Chehida, Amel ben, Kammoun, Thouraya, Barbu, Veronique, Boudawara, Tahya Sellami, Fakhfakh, Faiza, Khemakhem, Bassem, Sahnoun, Olfa Siala
Published in Annals of human genetics (01.05.2024)
Published in Annals of human genetics (01.05.2024)
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A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with sever nephropathy
Tabebi, Mouna, Mkaouar-Rebai, Emna, Mnif, Mouna, Kallabi, Fakhri, Ben Mahmoud, Afif, Ben Saad, Wafa, Charfi, Nadia, Keskes-Ammar, Leila, Kamoun, Hassen, Abid, Mohamed, Fakhfakh, Faiza
Published in Biochemical and biophysical research communications (10.04.2015)
Published in Biochemical and biophysical research communications (10.04.2015)
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Novel cases of Tunisian patients with mutations in the gene encoding 17β-hydroxysteroid dehydrogenase type 3 and a founder effect
Ben Rhouma, Bochra, Kallabi, Fakhri, Mahfoudh, Nadia, Ben Mahmoud, Afif, Engeli, Roger T., Kamoun, Hassen, Keskes, Leila, Odermatt, Alex, Belguith, Neila
Published in The Journal of steroid biochemistry and molecular biology (01.01.2017)
Published in The Journal of steroid biochemistry and molecular biology (01.01.2017)
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Molecular Analysis of Libyan Families with Allgrove Syndrome: Geographic Expansion of the Ancestral Mutation c.1331+1G>A in North Africa
Kallabi, Fakhri, Ben Rebeh, Imen, Felhi, Rahma, Sellami, Dorra, Masmoudi, Saber, Keskes, Leila, Kamoun, Hassen
Published in Hormone research in paediatrics (01.01.2016)
Published in Hormone research in paediatrics (01.01.2016)
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Journal Article
Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241 T > G mutation
Tabebi, Mouna, Charfi, Nadia, Kallabi, Fakhri, Alila-Fersi, Olfa, Mahmoud, Afif Ben, Tlili, Abdelaziz, Keskes-Ammar, Leila, Kamoun, Hassen, Abid, Mohamed, Mnif, Mouna, Fakhfakh, Faiza
Published in Journal of diabetes and its complications (01.01.2017)
Published in Journal of diabetes and its complications (01.01.2017)
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Splicing Defects in the AAAS Gene Leading to both Exon Skipping and Partial Intron Retention in a Tunisian Patient with Allgrove Syndrome
Kallabi, Fakhri, Ben Rhouma, Bochra, Baklouti, Siwar, Ghorbel, Rania, Felhi, Rahma, Keskes, Leila, Kamoun, Hassen
Published in Hormone research in paediatrics (2016)
Published in Hormone research in paediatrics (2016)
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Journal Article
Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation
Kallabi, Fakhri, Ellouz, Emna, Tabebi, Mouna, Ben Salah, Ghada, Kaabechi, Naziha, Keskes, Leila, Triki, Chahnez, Kamoun, Hassen
Published in Clinica chimica acta (30.01.2016)
Published in Clinica chimica acta (30.01.2016)
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Polymorphisms of glutathione S-transferases M1, T1, P1 and A1 genes in the Tunisian population: An intra and interethnic comparative approach
Ben Salah, Ghada, Kallabi, Fakhri, Maatoug, Sirine, Mkaouar-Rebai, Emna, Fourati, Amine, Fakhfakh, Faiza, Ayadi, Hamadi, Kamoun, Hassen
Published in Gene (01.05.2012)
Published in Gene (01.05.2012)
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Journal Article
Novel cases of Tunisian patients with mutations in the gene encoding 17ß-hydroxysteroid dehydrogenase type 3 and a founder effect
Rhouma, Bochra Ben, Kallabi, Fakhri, Mahfoudh, Nadia, Mahmoud, Afif Ben, Engeli, Roger T, Kamoun, Hassen, Keskes, Leila, Odermatt, Alex, Belguith, Neila
Published in The Journal of steroid biochemistry and molecular biology (01.01.2017)
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Published in The Journal of steroid biochemistry and molecular biology (01.01.2017)
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Cytocompatibility, gene-expression profiling, apoptotic, mechanical and (29)Si, (31)P solid-state nuclear magnetic resonance studies following treatment with a bioglass-chitosan composite
Samira, Jebahi, Hassane, Oudadesse, Mongi, Saoudi, Fakhri, Kallabi, Pellen, Pascal, Treq, Rebai, Abdelfatteh, Elfeki, Hassib, Keskes
Published in Biotechnology letters (01.12.2014)
Published in Biotechnology letters (01.12.2014)
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Journal Article
Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome
Kallabi, Fakhri, Belghuith, Neila, Aloulou, Hajer, Kammoun, Thouraya, Ghorbel, Soufiane, Hajji, Mouna, Gallas, Syrine, Chemli, Jaleleddine, Chabchoub, Imen, Azzouz, Hatem, Ben Chehida, Amel, Sfaihi, Lamia, Makni, Saloua, Amouri, Ali, Keskes, Leila, Tebib, Neji, Ben Becher, Saayda, Hachicha, Monjia, Kamoun, Hassen
Published in Archives of medical research (01.02.2016)
Published in Archives of medical research (01.02.2016)
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Journal Article
Cytocompatibility, gene-expression profiling, apoptotic, mechanical and super(29)Si, super(31)P solid-state nuclear magnetic resonance studies following treatment with a bioglass-chitosan composite
Samira, Jebahi, Hassane, Oudadesse, Mongi, Saoudi, Fakhri, Kallabi, Pellen, Pascal, Treq, Rebai, Abdelfatteh, Elfeki, Hassib, Keskes
Published in Biotechnology letters (01.12.2014)
Published in Biotechnology letters (01.12.2014)
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Journal Article
Cytocompatibility, gene-expression profiling, apoptotic, mechanical and ^sup 29^Si, ^sup 31^P solid-state nuclear magnetic resonance studies following treatment with a bioglass-chitosan composite
Samira, Jebahi, Hassane, Oudadesse, Mongi, Saoudi, Fakhri, Kallabi, Pellen, Pascal, Treq, Rebai, Abdelfatteh, Elfeki, Hassib, Keskes
Published in Biotechnology letters (01.12.2014)
Published in Biotechnology letters (01.12.2014)
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Journal Article
A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with sever nephropathy
Tabebi, Mouna, Mkaouar-Rebai, Emna, Mnif, Mouna, Kallabi, Fakhri, Ben Mahmoud, Afif, Ben Saad, Wafa, Charfi, Nadia, Keskes-Ammar, Leila, Kamoun, Hassen, Abid, Mohamed, Fakhfakh, Faiza
Published in Biochemical and biophysical research communications (2015)
Published in Biochemical and biophysical research communications (2015)
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Journal Article
Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation
Tabebi, Mouna, Charfi, Nadia, Kallabi, Fakhri, Alila-Fersi, Olfa, Ben Mahmoud, Afif, Tlili, Abdelaziz, Keskes-Ammar, Leila, Kamoun, Hassen, Abid, Mohamed, Mnif, Mouna, Fakhfakh, Faiza
Published in Journal of diabetes and its complications (01.01.2017)
Published in Journal of diabetes and its complications (01.01.2017)
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