Search Results - "Kamoun, F"

TRAPPC9 deficiency’s implication in “secondary” autism spectrum disorders by Majdoub, F, Bouzid, A, Souissi, A, Boujelbene, I, Bouchaala, W, Kamoun, F, M Ben said, Triki, C, Masmoudi, S, I Ben Ayed

“…IntroductionAutism spectrum disorder (ASD) is a highly heterogeneous neurodevelopmental disorder with many contributing risk genes. Multiple intellectual…”
Get full text

Caregiver burden in parents of children with neurological impairement and its relation with depression by Mellouli, A., Zouari, S., Smaoui, N., Bouchaala, W., Gassara, I., Jallouli, O., Feki, R., Ben Ncir, S., Kamoun, F., Maâlej, M., Charfi Triki, C.

“…Introduction Caregiving negatively affects the psychological and physical health of the caregivers, especially in parents of children with neurological…”
Get full text

Predictors of caregiver burden among parents of children with neurological impairement by Mellouli, A, Zouari, S, Smaoui, N, Jallouli, O, Omri, S, Bouchaala, W, Gassara, I, S Ben Nsir, Kamoun, F, Maâlej, M, C Charfi Triki

“…IntroductionMany neurological, sensory and behavioural deficits, are linked with significant limitations in the overall functioning not only of the child but…”
Get full text

Stabilization of clayey soils with Tunisian phosphogypsum: effect on geotechnical properties by Farroukh, Hajer, Mnif, T., Kamoun, F., Kamoun, L., Bennour, F.

“…Phosphogypsum and cement have been reported to improve the physicochemical properties of clayey soils. The present study aimed to investigate the behavior of…”
Get full text

Purification, amino acid sequence and characterization of Bacthuricin F4, a new bacteriocin produced by Bacillus thuringiensis by Kamoun, F, Mejdoub, H, Aouissaoui, H, Reinbolt, J, Hammami, A, Jaoua, S

“…Aims:  Purification and characterization of a new bacteriocin, Bacthuricin F4 of Bacillus thuringiensis. Methods and Results:  A newly isolated B…”
Get full text

RFID system management: state-of-the art and open research issues by Kamoun, F.

“…Radiofrequency identification (RFID) is an enabling technology that can provide organizations with unprecedented improved visibility and traceability of items…”
Get full text

Chylomicron retention disease: A rare cause of chronic diarrhea by Ben Ameur, S., Aloulou, H., Jlidi, N., Kamoun, F., Chabchoub, I., Di Filippo, M., Sfaihi, L., Hachicha, M.

“…Chylomicron retention disease (CRD) is a rare autosomal recessive hereditary hypocholesterolemic disorder. The disease most frequently presents in infants and…”
Get full text

Familial haemophagocytosis lymphohisticytosis type 3: A case report by Kamoun, F., Hsairi, M., Grandin, V., Ben Ameur, S., De Saint Basile, G., Hachicha, M.

“…Familial hemophagocytic lymphohistiocytosis (FHL) is a rare autosomal recessive disorder of immune regulation. Here, we report on a fatal case of type 3 FHL…”
Get full text

Unilateral to bilateral pleurisy: Pleural tuberculosis? by Ben Ameur, S, Smaoui, S, Kamoun, F, Chabchoub, I, Kamoun, T, Messaadi, F, Aloulou, H, Hachicha, M

“…Pleural tuberculosis is the first or second most common form of extrapulmonary tuberculosis as well as the main cause of pleural effusion in many countries. It…”
Get full text

Disseminated lymphangiomatosis: a rare cause of anemia by Ben Abdallah Chabchoub, R, Kamoun, F, Hidouri, S, Nouri, A, Hachicha, M, Mahfoudh, A

“…Disseminated lymphangiomatosis is a congenital lymphovenous vascular malformation. It can occur in different regions, some of which are unusual. The treatment…”
Get full text

An uncommon cause of hematemesis in children: factor XI deficiency by Kamoun, F, Sfaihi, L, Wali, M, Kamoun, T, Hachicha, M

“…Congenital factor XI deficiency, also called hemophilia C, is a rare coagulation disorder that is particularly common in Ashkenazi Jews. Individuals with…”
Get full text

Schimmelpenning-Feuerstein-Mims syndrome: a case report by Bahloul, E, Abid, I, Masmoudi, A, Makni, S, Kamoun, F, Boudawara, T, Triki, C, Turki, H

“…Schimmelpenning-Feuerstein-Mims syndrome (SFM) is a congenital neurocutaneous disorder characterized by the association of nevus sebaceous with extracutaneous…”
Get full text

Larval rearing and weaning of thick lipped grey mullet ( Chelon labrosus) in mesocosm with semi-extensive technology by Ben Khemis, I., Zouiten, D., Besbes, R., Kamoun, F.

“…The mullets are consumers of low trophic layers and can develop in a variety of biotopes. Despite research efforts on artificial propagation, mullet…”
Get full text

Psycho-emotional impact of a child's disability on parents by Ben Thabet, J, Sallemi, R, Hasïri, I, Zouari, L, Kamoun, F, Zouari, N, Triki, C, Maâlej, M

“…Care for a child with a disability is a stressful experience for parents. It triggers a range of emotions and feelings that require a set of behaviors and…”
Get full text

1502 Malformations of Cortical Development and Epilepsy: A Report of 13 Cases by Ameur, S Ben, Maaloul, I, Hmida, S Hadj, Aloulou, H, Sfaihi, L, Chabchoub, I, Kamoun, F, Kamoun, T, Mnif, Z, Hachicha, M

“…Background and Aims Malformations of cortical development MCDs are increasingly recognized as important causes of epilepsy. The aims of this study is to…”
Get full text

Triassic palaeogeography of Tunisia by Kamoun, F, Peybernès, B, Ciszak, R, Calzada, S

“…A stratigraphic, palaeogeographic and palinspastic synthesis of the Triassic successions in Tunisia is herein documented from a SSE-NNN oriented profile…”
Get full text

Aicardi syndrome associated with severe congenital ptosis by Chabchoub, I, Kamoun, F, Daoued, E, Ben Mansour, L, Kmiha, S, Kamoun, T, Mnif, Z, Hachicha, M

“…Aicardi syndrome is a rare neurodevelopmental disorder characterized by corpus callosum agenesis, chorioretinal lacunae and early-onset infantile spasms. We…”
Get full text

Une cause inhabituelle d’hématémèse chez l’enfant : le déficit en facteur XI by Kamoun, F., Sfaihi, L., Wali, M., Kamoun, T., Hachicha, M.

“…Le déficit congénital en facteur XI appelé aussi maladie de Rosenthal ou hémophilie C, est une maladie hémorragique rare par déficit constitutionnel en facteur…”
Get full text

P186 Hypokalemic periodic paralysis: case report by Kallel, R, Hsairi, I, Kamoun, F, Ayedi, F, Boudawara, T, Fakhfakh, F, Triki, C

Get full text

Dysthyroïdie et trisomie 21 by Kamoun, F., Dr, Kamoun, T., Dr, Loukil, S., Dr, Maaloul, I., Dr, Belguith, N., Dr, Chabchoub, I., Dr, Hachicha, M., Dr

“…Objectifs Étudier les différentes pathologies thyroïdiennes chez les patients trisomiques 21 et leur prise en charge thérapeutique. Matériels et méthodes Étude…”
Get full text