A rare cause of cyanosis: Congenital methemoglobinemia
Guedri, Rahma, Missaoui, Nada, Essaddam, Leila, Ben Becher, Saayda
Published in Clinical case reports (01.07.2021)
Published in Clinical case reports (01.07.2021)
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Journal Article
Single-center experience of congenital disorders of glycosylation syndrome screening in Tunisia: A retrospective study over a 15-year period (2007–2021)
Zidi, Wiem, Hadj-Taieb, Sameh, Kraoua, Ichraf, Hachicha, Mongia, Seboui, Hassen, Monastiri, Kamel, Becher, Saayda Ben, Turki, Ilhem, Sanhaji, Haifa, Tebib, Neji, Kaabachi, Naziha, Feki, Moncef, Allal-Elasmi, Monia
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.02.2024)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.02.2024)
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Journal Article
Implementation of effective transition from pediatric to adult diabetes care: epidemiological and clinical characteristics—a pioneering experience in North Africa
Essaddam, Leïla, Kallali, Wafa, Jemel, Manel, Kandara, Hager, Kammoun, Inès, Hsairi, Mohamed, Ben Salem, Leïla, Ben Becher, Saayda
Published in Acta diabetologica (01.11.2018)
Published in Acta diabetologica (01.11.2018)
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Journal Article
Characteristics and etiologies of short stature in children: Experience of an endocrine clinic in a Tunisian tertiary care hospital
Essaddam, Leïla, Kallali, Wafa, Cherifi, Emna, Guedri, Rahma, Mattoussi, Nadia, Fitouri, Zohra, Ben Becher, Saayda
Published in International journal of pediatrics & adolescent medicine (01.06.2020)
Published in International journal of pediatrics & adolescent medicine (01.06.2020)
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Journal Article
Congenital hypothyroidism presenting with reversible renal impairment: an under-recognised problem?
Essaddam, Leïla, Ben Mansour, Asma, Missaoui, Nada, Guedri, Rahma, Mattoussi, Nadia, Fitouri, Zohra, Ben Becher, Saayda
Published in Journal of diabetes and metabolic disorders (01.12.2019)
Published in Journal of diabetes and metabolic disorders (01.12.2019)
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Journal Article
Validation of the Arabic and Tunisian Arabic version of the KINDL questionnaires for children with diabetes type 1
Essaddam, Leïla, Ben Mansour, Asma, Ben Amor, Arwa, Ravens-Sieberer, Ulribe, Klein, Toni Maria, Ben Becher, Saayda
Published in Libyan journal of medicine (01.01.2019)
Published in Libyan journal of medicine (01.01.2019)
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Journal Article
Tuberculous meningitis in Bacille Calmette-Guerin-vaccinated children: clinical spectrum and outcome
Khemiri, Monia, Bagais, Abderrahmen, Becher, Saayda Ben, Bousnina, Souad, Bayoudh, Fethi, Mehrezi, Ahmed, Lakhoua, Rachid, Barsaoui, Siham
Published in Journal of child neurology (01.06.2012)
Published in Journal of child neurology (01.06.2012)
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Journal Article
P079 Multi-systemic inflammatory syndrome in children: skin tropism
Guedri, Rahma, Glai, Mariem, Fitouri, Zohra, Ben Becher, Saayda
Published in Rheumatology (Oxford, England) (11.11.2021)
Published in Rheumatology (Oxford, England) (11.11.2021)
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Journal Article
P034 Macrophage activation syndrome in Juvenile Idiopathic Arthritis
Guedri, Rahma, Glaimeriem, Fitouri, Zohra, Ben Becher, Saayda, Hamza, Bechir
Published in Rheumatology (Oxford, England) (11.11.2021)
Published in Rheumatology (Oxford, England) (11.11.2021)
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Journal Article
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype
Motta, Marialetizia, Fasano, Giulia, Gredy, Sina, Brinkmann, Julia, Bonnard, Adeline Alice, Simsek-Kiper, Pelin Ozlem, Gulec, Elif Yilmaz, Essaddam, Leila, Utine, Gulen Eda, Guarnetti Prandi, Ingrid, Venditti, Martina, Pantaleoni, Francesca, Radio, Francesca Clementina, Ciolfi, Andrea, Petrini, Stefania, Consoli, Federica, Vignal, Cédric, Hepbasli, Denis, Ullrich, Melanie, de Boer, Elke, Vissers, Lisenka E.L.M., Gritli, Sami, Rossi, Cesare, De Luca, Alessandro, Ben Becher, Saayda, Gelb, Bruce D., Dallapiccola, Bruno, Lauri, Antonella, Chillemi, Giovanni, Schuh, Kai, Cavé, Hélène, Zenker, Martin, Tartaglia, Marco
Published in American journal of human genetics (04.11.2021)
Published in American journal of human genetics (04.11.2021)
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Journal Article
A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients
Ben-Khemis, Leila, Mekki, Najla, Ben-Mustapha, Imen, Rouault, Karen, Mellouli, Fethi, Khemiri, Monia, Bejaoui, Mohamed, Essaddam, Leila, Ben-Becher, Saayda, Boughamoura, Lamia, Hassayoun, Saida, Ben-Ali, Meriem, Barbouche, Mohamed-Ridha
Published in Molecular immunology (01.10.2017)
Published in Molecular immunology (01.10.2017)
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Journal Article
Respiratory forms of COVID-19 in children: clinical characteristics and outcomes in a Tunisian hospital
Khalsi, Fatma, Kbaier, Soumaya, Belhadj, Imen, Aba, Neila Ben, Meftah, Khawla, Khemiri, Monia, Boukthir, Samir, Becher, Saayda Ben, Smaoui, Hanen, Boussetta, Khadija
Published in PAMJ clinical medicine (2024)
Published in PAMJ clinical medicine (2024)
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Journal Article
Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT)
Essaddam, Leila, Zitouni, Ons, Kraoua, Lilia, Trabelsi, Madiha, Sassi, Hella, Kmiha, Sana, Charfi, Fatma, El Guiche, Dorra, Kebaïli, Raoudha, Jaballah, Nesrine, Rjeb, Maroua, Zouari, Noura, El Aribi, Yasmina, Hizem, Syrine, Wannes, Salmen, Fkih Romdhane, Ibtihel, Sfar, Mohamed Tahar, Ben Hamouda, Hechmi, Hadj Salem, Radhia, Khlayfia, Zied, Khmiss, Tarek, Monastiri, Kamel, Siala, Nadia, Chouchane, Slaheddine, Souaa, Habib, Khochtali, Inès, Mahjoub, Bahri, Sfar, Habib, Ben Jemâa, Lamia, Abroug, Saoussen, Boughamoura, Lamia, Kamoun, Inès, Kamoun, Thouraya, Mrad, Ridha, Ben Becher, Saayda
Published in Journal of Pediatric Endocrinology & Metabolism (27.06.2023)
Published in Journal of Pediatric Endocrinology & Metabolism (27.06.2023)
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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
C677t polymorphism of MTHFR and G80A polymorphism of RFC genes and their relation with homocysteine levels in obese Tunisian children
Gara, Sonia, Ochi, Hanene, Chango, Abalo, Najjar, Latifa, Feki, Moncef, B'chir, Fattouma, Kaabachi, Neziha, Ben Becher, Saayda, Boukthir, Samir, Abdennebi, Monia
Published in Tunisie Medicale (01.06.2011)
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Published in Tunisie Medicale (01.06.2011)
Journal Article
Congenital lobar emphysema. Report of 17 cases
Khemiri, Monia, Khaldi, Faouzia, Ben Becher, Saayda, Chaouachi, Beji, Houissa, Taoufik, Barsaoui, Siham
Published in Tunisie Medicale (01.04.2008)
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Published in Tunisie Medicale (01.04.2008)
Journal Article
A rare cause of cyanosis: Congenital methemoglobinemia
Guedri, Rahma, Missaoui, Nada, Essaddam, Leila, Ben Becher, Saayda
Published in Clinical case reports (01.07.2021)
Published in Clinical case reports (01.07.2021)
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Report
Congenital hypothyroidism presenting with reversible renal impairment: an under-recognised problem?
Essaddam, Leïla, Ben Mansour, Asma, Missaoui, Nada, Guedri, Rahma, Mattoussi, Nadia, Fitouri, Zohra, Ben Becher, Saayda
Published in Journal of diabetes and metabolic disorders (01.12.2019)
Published in Journal of diabetes and metabolic disorders (01.12.2019)
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Report
Autoimmune polyglandular syndrome type I
Matoussi, Nadia, Aissa, Khaoula, Fitouri, Zohra, Makni, Saloua, Ben Becher, Saayda
Published in Tunisie Medicale (01.05.2008)
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Published in Tunisie Medicale (01.05.2008)
Journal Article