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Thouraya Kammoun

Observed names: Kammoun Thouraya, T Kammoun, T. Kammoun
ORCID: 0000-0002-1731-6162
Observed ORCID: 0000-0002-1731-6162
OpenAlex ID: A5090345852
Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome
2016 · Fakhri Kallabi, Neila Belghuith, et al. · Archives of Medical Research · 32
Association of TCR/CD3, PTPN22, CD28 and ZAP70 gene polymorphisms with type 1 diabetes risk in Tunisian population: Family based association study
2014 · Zouidi Ferjeni, D. Bouzid, et al. · Immunology Letters · 28
Association of BANK1 and cytokine gene polymorphisms with type 1 diabetes in Tunisia
2013 · Ferjani Zouidi, Mouna Stayoussef, et al. · Gene · 24
A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNAIle m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss
2010 · Imen Chamkha, Emna Mkaouar-Rebai, et al. · Biochemical and Biophysical Research Communications · 21
Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNATrp in patients with Leigh syndrome
2009 · Emna Mkaouar-Rebai, Imen Chamkha, et al. · Molecular Genetics and Metabolism · 20
Contribution of PTPN22, CD28, CTLA-4 and ZAP-70 variants to the risk of type 1 diabetes in Tunisians
2013 · Ferjeni Zouidi, Mouna Stayoussef, et al. · Gene · 19
Molecular Investigation of Distal Renal Tubular Acidosis in Tunisia, Evidence for Founder Mutations
2014 · Majdi Nagara, Konstantinos Voskarides, et al. · Genetic Testing and Molecular Biomarkers · 17
A case of Kearns–Sayre syndrome with two novel deletions (9.768 and 7.253kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles
2010 · Emna Mkaouar-Rebai, Imen Chamkha, et al. · Mitochondrion · 15
Descriptive analyses of Turner syndrome: 49 cases in Tunisia
2010 · M. Elleuch, M. Mnif Feki, et al. · Annales d Endocrinologie · 14
A novel MT-CO2 m.8249G > A pathogenic variation and the MT-TW m.5521G > A mutation in patients with mitochondrial myopathy
2013 · Emna Mkaouar-Rebai, Afif Ben Mahmoud, et al. · Mitochondrial DNA · 12
Vascularite avec atteinte rénale et anticorps anticytoplasme des polynucléaires neutrophiles (ANCA) après prise de benzylthio-uracile chez l'enfant
2007 · Mongia Hachicha, Thouraya Kammoun, et al. · Néphrologie & Thérapeutique · 11
Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome
2018 · Marwa Maalej, Thouraya Kammoun, et al. · Biochemical and Biophysical Research Communications · 10
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation
2021 · Mariam Moalla, Wajdi Safi, et al. · Frontiers in Endocrinology · 7
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A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNASer(UCN) genes in a patient with hearing impairment, diabetes and congenital visual loss
2012 · Emna Mkaouar-Rebai, Imen Chamkha, et al. · Biochemical and Biophysical Research Communications · 7
A Tunisian patient with Pearson syndrome harboring the 4.977 kb common deletion associated to two novel large-scale mitochondrial deletions
2011 · Imen Ben Ayed, Imen Chamkha, et al. · Biochemical and Biophysical Research Communications · 7
La fibroscopie digestive chez l’enfant : indications et résultats : expérience d’un service de pédiatrie générale
2011 · H. Aloulou, I. Maaloul, et al. · Journal de Pédiatrie et de Puériculture · 7
Identification of a novel homozygous mutation in NAXE gene associated with early-onset progressive encephalopathy by whole-exome sequencing: in silico protein structure characterization, molecular docking, and dynamic simulation
2022 · Marwa Maalej, Lamia Sfaihi, et al. · Neurogenetics · 6
La maladie de Cowden : une nouvelle observation pédiatrique
2006 · M. Hachicha, T. Kammoun, et al. · Archives de Pédiatrie · 6
CREM variant rs17583959 conferred susceptibility to T1D risk in the Tunisian families
2016 · Ferjani Zouidi, D. Bouzid, et al. · Immunology Letters · 5
[Epidemiological, etiological and evolutionary aspects of children cirrhosis in a developing country: experience of the pediatric department of SFAX University hospital, Tunisia].
2007 · Malek Chaabouni, Sonia Bahloul, et al. · PubMed · 5
Déficit congénital en facteur VII de la coagulation, révélé par une hémorragie cérébrale
2009 · L. Sfaihi Ben Mansour, A. Thabet, et al. · Archives de Pédiatrie · 4
Hypoparathyroidism in children: a study of eight cases.
2018 · Ines Maaloul, Hajer Aloulou, et al. · PubMed · 3
Association between the IL2RA polymorphism and type 1 diabetes risk: Family based association study
2016 · Zouidi Ferjani, D. Bouzid, et al. · Meta Gene · 3
L’hypoplasie de la carotide interne : une cause rare d’accident vasculaire cérébral ischémique chez l’enfant
2010 · L. Sfaihi, A. Boukedi, et al. · Archives de Pédiatrie · 3
Occurrence of Hypopituitarism in Tunisian Turner Syndrome patients: familial versus sporadic cases
2021 · M. Mnif-Feki, W. Safi, et al. · Gynecological Endocrinology · 2
Works count: 68
Citation count: 297
H-index: 11
I10-index: 12
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