Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Mkaouar, Rahma, Riahi, Zied, Charfeddine, Cherine, Chelly, Imen, Boudabbous, Hela, Dallali, Hamza, Bonnet, Crystel, Hechmi, Meriem, Bekri, Soumeya, Zitouna, Nadia, Zekri, Lotfi, Tounsi, Amel, Kefi, Rym, Marrakchi, Jihene, Messaoud, Olfa, Kraoua, Ichraf, Maalej, Sonia, Turki Ben Youssef, Ilhem, Ben Hmid, Ahlem, Giraudet, Fabrice, Bouchoucha, Sami, Tebib, Neji, Besbes, Ghazi, Petit, Christine, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha
Published in PloS one (06.10.2021)
Published in PloS one (06.10.2021)
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P126 Drug poisoning in children: Data of Tunisian pediatric department
Barbaria, Wiem, Maalaoui, Hager, Belhassen, Ferchichi, Hammami, Olfa, Chelly, Imen, Khamassi, Ichrak
Published in Resuscitation (01.06.2022)
Published in Resuscitation (01.06.2022)
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P128 Carbon monoxide intoxication in children in a Tunisian pediatric unit
Barbaria, Wiem, Maalaoui, Hager, Manel, Bourcheda, Mechlia, Salma, Hamami, Olfa, Chelly, Imen, Khamassi, Ichrak
Published in Resuscitation (01.06.2022)
Published in Resuscitation (01.06.2022)
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P130 Clinical profile and management of diabetic ketoacidosis in a Tunisian pediatric unit
Barbaria, Wiem, Aloulou, Jassem, Ben Said, Molka, Hammami, Olfa, Chelly, Imen, Khamassi, Ichrak
Published in Resuscitation (01.06.2022)
Published in Resuscitation (01.06.2022)
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P127 Cardiac complications in children with multisystem inflammatory syndrome
Barbaria, Wiem, Kharbech, Nouha, Soua, Amani, Bougdar, Amal, Hammami, Olfa, Chelly, Imen, Khamassi, Ichrak
Published in Resuscitation (01.06.2022)
Published in Resuscitation (01.06.2022)
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Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients
Trabelsi, Mediha, Nouira, Malek, Maazoul, Faouzi, Kraoua, Lilia, Meddeb, Rim, Ouertani, Ines, Chelly, Imen, Benoit, Valérie, Besbes, Ghazi, Mrad, Ridha
Published in International journal of pediatric otorhinolaryngology (01.12.2017)
Published in International journal of pediatric otorhinolaryngology (01.12.2017)
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Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy
Trabelsi, Mediha, Chelly, Imen, Maazoul, Faouzi, Chaabouni, Myriam, Ouertani, Ines, Kraoua, Lilia, Khemakhem, Lamia, Mrad, Ridha, Chaabouni, Habiba
Published in European journal of medical genetics (01.01.2013)
Published in European journal of medical genetics (01.01.2013)
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Hexasomy of the Prader–Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: Case report
Kraoua, Lilia, Chaabouni, Myriam, Ewers, Elisabeth, Chelly, Imen, Ouertani, Ines, Ben Jemaa, Lamia, Maazoul, Faouzi, Liehr, Thomas, Chaabouni, Habiba
Published in European journal of medical genetics (01.07.2011)
Published in European journal of medical genetics (01.07.2011)
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Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients
Ouertani, Ines, Chaabouni, Myriam, Chelly, Imen, Kraoua, Lilia, Maazoul, Faouzi, Trabelsi, Mediha, Meddeb, Rym, Boussaada, Rafik, Azzouz, Hatem, Charfi, Fatma, Hamida, Emira Ben, Meherzi, Ahmed, Mrad, Ridha, Bouhamed-Chaabouni, Habiba
Published in Open journal of genetics (2014)
Published in Open journal of genetics (2014)
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