Search Results - "Fekih, Moncef"

Toxicological evaluation of oral exposure to isoniazid: behavioral, biochemical, and histopathological assessments in rats by Ben Said, Dorra, Dahmani, Israa, Ben Ali, Ridha, Bassem, Hammami, El Fekih, Moncef, Chedly, Achraf, Elmay, Michelle-Véronique, Gaies, Emna, El Aidli, Sihem

“…Isoniazid (INH), being the first-line drug used as an anti-tuberculosis drug, is known to be associated with physiological deteriorations including hepatic and…”
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Identification of patients with abetalipoproteinemia and homozygous familial hypobetalipoproteinemia in Tunisia by Najah, Mohamed, Di Leo, Enza, Awatef, Jelassi, Magnolo, Lucia, Imene, Jgurim, Pinotti, Elisa, Bahri, Mahjoub, Barsaoui, Sihem, Brini, Ines, Fekih, Moncef, Slimane, Mohamed Naceur, Tarugi, Patrizia

“…Abetalipoproteinemia (ABL) and Homozygous Familial Hypobetalipoproteinemia (Ho-FHBL) are rare monogenic diseases characterised by very low plasma levels of…”
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Is BNP assay useful for the diagnosis of acute dyspnea in emergencies departments? by Lakhdhar, Rim, Hamouda, Chokri, Ben Ammar, Lotfi, Majed, Kamel, Moncef, Fekih, Kaabachi, Naziha, Drissa, Habiba, Borsali Falfoul, Nebiha

“…It would be interesting to the emergency doctor to have at his disposal a helpful diagnostic tool like brain natriuretic peptide (BNP). Such assay is simple,…”
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Bone metabolism, biochemical markers of bone resorption and formation processes and interleukine 6 cytokin level during coeliac disease by Fekih, Monia, Sahli, Hela, Ben Mustapha, Nadia, Mestiri, Imen, Fekih, Moncef, Boubaker, Jalel, Kaabachi, Naziha, Sellami, Mohamed, Kallel, Lamia, Filali, Azza

“…Celiac disease (CD) is characterized by a malabsorption syndrom. The bone anomalies are one of the principal complications of this disease. The osteoporosis…”
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Congenital hyperinsulinism: review of 12 Tunisian cases by Ben Turkia, Hadhami, Brahim, Karima, Azzouz, Hatem, Tebib, Neji, Abdelmoula, Mohamed Slim, Ben Chehida, Amel, Fekih, Moncef, Sayed, Sadok, Kaabar, Nejib, Francoise Ben Dridi, Marie

“…Congenital hyperinsulinism in infancy (CHI) is a heterogeneous disorder with respect to genetics and response to therapy. Data on CHI are sporadic in North…”
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HLA Class II Alleles Susceptibility Markers of Type 1 Diabetes Fail to Specify Phenotypes of Ketosis-Prone Diabetes in Adult Tunisian Patients by Laadhar, Lilia, Harzallah, Fatma, Zitouni, Mondher, Kallel-Sellami, Maryam, Fekih, Moncef, Kaabachi, Naziha, Slimane, Hádia, Makni, Sondès

“…We aimed to characterize the different subgroups of ketosis-prone diabetes (KPD) in a sample of Tunisian patients using the Aβ scheme based on the presence or…”
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