Search Results - "Boussetta, K."

Phenotypic and genotypic characterization of meningococcal isolates in Tunis, Tunisia: High diversity and impact on vaccination strategies by Brik, A., Terrade, A., Hong, E., Deghmane, A., Taha, M.K., Bouafsoun, A., Khmiri, M., Boussetta, K., Boukhir, S., Jaballah, N. Ben, Kechrid, A., Smaoui, H.

“…[Display omitted] •In Tunisia, Neisseria meningitidis serogroup B (MenB) is the leading cause of invasive meningococcal diseases.•We report high rates of…”
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Impact of illness on mothers of children with cystic fibrosis in Tunisia: A qualitative interview study: Impact of cystic fibrosis on Tunisian mothers by Hamouda, S, Hadj, I Bel, Sayari, T, Louati, A, Messaoud, T, Khalsi, F, Boussetta, K

“…Caring for a child with cystic fibrosis (CF) is challenging and stressful and even more so in a country with limited resources. Our aim was to study the impact…”
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Hemophagocytic lymphohistiocytosis associated with an IgG Cold agglutinin by Jouini, H., Chouaieb, S., Boussetta, K., Toumi, N.E.H.

“…Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disease eventually caused or reactivated by a viral infection, which can also lead to the…”
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Thiamine responsive megaloblastic anemia mimicking mitochondrial disorders by Tinsa, F., Hechmi, M., Hadj, I.B., Khalsi, F., Chargui, M., Kefi, R., Azouz, H., Boussetta, K., Abdelhak, S.

“…Letter to the Editor…”
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A novel large deletion in CCM1 gene in a Tunisian family by Tinsa, F., Bel Hadj, I., Riant, F., Ben Romdhane, M., Brini, I., Tournier-Lasserve, E., Louati, H., Abdelhak, S., Hamouda, S., Boussetta, K.

“…Familial CCM is a rare entity associated with the mutation of three genes: CCM1 (KRIT1), CCM2 (MGC4607), and CCM3 (PDCD10). We report here the first…”
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Hypersensitivity reactions to paracetamol in children: a study of 25 cases by Boussetta, K., Ponvert, C., Karila, C., Bourgeois, M. Le, Blic, J., Scheinmann, P.

“…Background:  Allergic‐like reactions to paracetamol (acetaminophen) are rare. Paracetamol allergic and nonallergic hypersensitivity (HS) has been diagnosed in…”
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Contribution of M470V variant to cystic fibrosis: First study in CF and normal Tunisian population by Nefzi, M., Hadj Fredj, S., Tebib, N., Barsaoui, S., Boussetta, K., Siala, H., Messaoud, T.

“…Determining the frequency of M470V polymorphism in cystic fibrosis and healthy cohort in Tunisia to establish the contribution of M470V polymorphism in cystic…”
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Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation by Tinsa, F, Chebbi, Y, Meddeb, M, Bousnina, D, Boussetta, K, Bousnina, S

“…A male infant with partial monosomy 10 q and partial trisomy 11q as a result of de novo unbalanced translocation between the long arms of chromosomes 10 and…”
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Lipoblastome cervico-médiastinal chez l’enfant by Ghribi, A., Gasmi, M., Ben Slama, A., Ben Salah, M., Boussetta, K., Hamzaoui, M.

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Kernicterus secondary to henna application in a neonate with G6PD deficiency: A case report by Dabboubi, R., Ouali, F., Hadj Fraj, S., Baccouche, I., Chalbi, S., Othmani, M., Boussetta, K., Taieb, M.

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Clinical expression of patients with the E1104X cystic fibrosis mutation in Tunisian and Libyan population by Hadj Fredj, S., Sahli, C., Ouali, F., Othmani, R., Chelbi, S., Othmani, M., Dabboubi, R., Khalsi, F., Hamouda, S., Boussetta, K., Messaoud, T.

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Impact of illness on mothers of children with cystic fibrosis in Tunisia: A qualitative interview study by Hamouda, S., Hadj, I.Bel, Sayari, T., Louati, A., Messaoud, T., Khalsi, F., Boussetta, K.

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A Tunisian neonatal case of co-inheritance of G6PD deficiency and HBC presenting as severe jaundice and hemolytic anemia by Dabboubi, R., Fredj, S. Hadj, Ghaffar, I. Ben, Siala, H., Boussetta, K., Messaoud, T.

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Implication of polymorphic marker IVS6A GATT in the clinical expression of cystic fibrosis by Sahli, C., Fredj, S. Hadj, Boussetta, K., Meherzi, A., Messaoud, T.

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Identification of a mild cystic fibrosis mutation 2789+5 G to a for the first time in Tunisian population by Fredj, S. Hadj, Sahli, C., Dabboubi, R., Hadj, I. Bel, Othmani, R., Dridi, S., Boussetta, K., Messaoud, T.

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Asthme de l’enfant et Covid 19 : population à risque ? by Trabelsi, I., Briki, I., Khalsi, F., Belhadj, I., Missaoui, N., Khemiri, M., Smaoui, H., Ben Bêcher, S., Ben Romdhane, M., Boussetta, K.

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Profil de sensibilisation chez l’enfant asthmatique by Khalsi, F., Kbaier, S., Turki, A., Trabelsi, I., Belhadj, I., Boussetta, K.

“…L’asthme est une maladie inflammatoire chronique, considérée comme la résultante d’interactions complexes entre des facteurs génétiques et des facteurs…”
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Simulcast-based DCA scheme for unicast and multicast communications in LEO satellite networks by Boussetta, K., Doudane, Y.G., Beylot, A.-L.

“…We investigate a downlink channel assignment scheme for multipoint communications and we propose a new simulcast-based dynamic channel assignment policy for…”
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Connaissances et perceptions des parents d’enfants asthmatiques by Khalsi, F., Mansouri, H., Briki, I., Kbaier, S., Trabelsi, I., Belhadj, I., Boussetta, K.

“…L’éducation thérapeutique (ETP) des parents et leur sensibilisation autour de la maladie asthmatique constituent des étapes incontournables dans la prise en…”
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Rerouting algorithm for non real time traffic by Gueroui, A., Boussetta, K., Gaiti, D.

“…The third generation of wireless networks will be broadband and thus will be able to support several services with different constraints on their QoS such as…”
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