15 results on '"Brahim, W"'
Search Results
2. CALM-AF10+ T-ALL expression profiles are characterized by overexpression of HOXA and BMI1 oncogenes
- Author
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Dik, W A, Brahim, W, Braun, C, Asnafi, V, Dastugue, N, Bernard, O A, van Dongen, J J M, Langerak, A W, Macintyre, E A, and Delabesse, E
- Published
- 2005
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3. La surpression pulmonaire avec aéroembolisme cérébral au cours de la plongée sous-marine
- Author
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Sassi, R. Ben, Brahim, W. Belhaj, Mezoughi, I., Gharsallah, H., Hajjej, Z., and Trabelsi, W.
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- 2014
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4. Statut en vitamine D d’une population de femmes obèses
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Ounaissa, K., Oueslati, I., Ben Brahim, W., Harrabi, T., Ben Naceur, K., Sallemi, S., Ben Brahim, A., Abdessalem, H., Yahyaoui, R., Jamoussi, H., and Amrouche, C.
- Published
- 2018
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5. Les facteurs de risque nutritionnels de présarcopénie dans une population de femmes obèses
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Ounaissa, K., Smida, A., Harrabi, T., Ben Brahim, W., Chelbi, S., Sallemi, S., Oueslati, I., Bendag, N., Bou Meftah, S., Abdesselem, H., Jamoussi, H., and Amrouch, C.
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- 2018
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6. Prévalence de la sarcopénie dans un groupe de femmes adultes obèses
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Ounaissa, K., Sellami, S., Ben Brahim, W., Harrabi, T., Bendag, N., Ben Naceur, K., Ben Brahim, A., Abdessalem, H., Yahyaoui, R., Jamoussi, H., and Amrouche, C.
- Published
- 2018
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7. Communicating climate change and biodiversity loss with local populations: exploring communicative utopias in eight transdisciplinary case studies.
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Ansari D, Schönenberg R, Abud M, Becerra L, Brahim W, Castiblanco J, de la Vega-Leinert AC, Dudley N, Dunlop M, Figueroa C, Guevara O, Hauser P, Hobbie H, Hossain MAR, Hugé J, Janssens de Bisthoven L, Keunen H, Munera-Roldan C, Petzold J, Rochette AJ, Schmidt M, Schumann C, Sengupta S, Stoll-Kleemann S, van Kerkhoff L, Vanhove MPM, and Wyborn C
- Abstract
Climate change and biodiversity loss trigger policies targeting and impacting local communities worldwide. However, research and policy implementation often fail to sufficiently consider community responses and to involve them. We present the results of a collective self-assessment exercise for eight case studies of communications with regard to climate change or biodiversity loss between project teams and local communities. We develop eight indicators of good stakeholder communication, reflecting the scope of Verran's (2002) concept of postcolonial moments as a communicative utopia. We demonstrate that applying our indicators can enhance communication and enable community responses. However, we discover a divergence between timing, complexity and (introspective) effort. Three cases qualify for postcolonial moments, but scrutinising power relations and genuine knowledge co-production remain rare. While we verify the potency of various instruments for deconstructing science, their sophistication cannot substitute trust building and epistemic/transdisciplinary awareness. Lastly, we consider that reforming inadequate funding policies helps improving the work in and with local communities., Competing Interests: Research ethics statementNot applicable to this article.Consent for publication statementThe authors declare that research participants’ informed consent to publication of findings – including photos, videos and any personal or identifiable information – was secured prior to publication.Conflicts of interest statementThe authors declare no conflicts of interest with this work.The authors declare no conflicts of interest with this work., (© 2023 The Authors.)
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- 2023
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8. Multimodality Imaging Assessment of Ischemic-Related Submitral Left Ventricular Pouch: A Case Report.
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Machraa A, Fertat O, Ben Brahim W, Oukerraj L, and Cherti M
- Abstract
Submitral left ventricular aneurysm remains a rare condition with a varied etiology besides the congenital origin. We describe the case of a 62-year-old male patient who presented, two weeks after an inferobasal myocardial infarction (MI), with dyspnea and atypical chest pain. Transthoracic echocardiography (TTE) and cardiac computed tomography (CT) revealed a giant thin-walled submitral left ventricular aneurysm. He was managed conservatively given the high operative risk. The overall survival was five months after discharge. Despite its rarity, recognizing the causal relationship between ischemic heart disease and submitral aneurysm can prevent life-threatening complications and is therefore of major importance. In the era of advanced imaging, multimodality cardiac imaging techniques are a key element for guiding diagnostic and therapeutic strategies., Competing Interests: The authors have declared that no competing interests exist., (Copyright © 2023, Machraa et al.)
- Published
- 2023
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9. Sustained ventricular arrhythmia and sinus node dysfunction revealing a cardiac amyloidosis: A case report.
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Machraa A, Ben Brahim W, Sidaty O, Fellat R, and Fellat N
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Introduction and Importance: Amyloidosis is an infiltrative multisystem disease due to extracellular deposition of fibrils in tissues and organs. Cardiac involvement can result in progressive heart failure, conduction abnormalities and arrhythmias and is associated with a poor prognosis. Atrial arrhythmias and non-sustained ventricular arrhythmias are the most common arrhythmias in cardiac amyloidosis. However, the association of sinus node dysfunction and sustained ventricular arrhythmia is quite exceptional., Case Presentation: A 59-year-old male patient was admitted with a gradually worsening dyspnea with a lipothymic discomfort. Upon emergency department, an initial electrocardiogram revealed a severe bradycardia related to a sinus node dysfunction. A transthoracic echocardiography and cardiac magnetic resonance imaging showed features suspicious for cardiac amyloidosis. The diagnosis of AL cardiac amyloidosis with multiple myeloma was confirmed based on histological evidence. During hospitalization, the patient presented a sustained unstable ventricular tachycardia which has been converted by electrical cardioversion. He was treated with an implantable cardioverter-defibrillator (ICD) for secondary prevention with one episode of appropriate therapy. Unfortunately, the patient died few weeks later., Clinical Discussion: The AL subtype of cardiac amyloidosis is associated with higher rates of arrhythmias, especially VT. The management of arrhythmias in cardiac amyloidosis is complex and remains challenging given the lack of evidence. ICD was not associated with longer survival; these findings underscore the importance of careful patient selection for ICD., Conclusion: As prognosis improves with the advances made in the medical treatment of cardiac amyloidosis, further studies are required to guide the management of all types of arrhythmias in cardiac amyloidosis., Competing Interests: All the authors declare that they have no competing interests., (© 2022 The Authors.)
- Published
- 2022
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10. Epidemiological characteristics, management, and outcomes of atrial fibrillation in TUNISIA: Results from the National Tunisian Registry of Atrial Fibrillation (NATURE-AF).
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Ouali S, Ben Halima A, Chabrak S, Chettaoui R, Ben Halima M, Haggui A, Krichane S, Noureddine L, Marrakchi S, Charfeddine S, Hassine M, Sayahi K, Abbes Mohamed F, Nasraoui W, Ajmi H, Ben Miled M, Jebbari Z, Meghaieth MA, Allouche E, Mechmeche R, Zakhama L, Sdiri W, Ben Khalfallah A, Gharbi A, Milouchi S, Neji A, Antit S, Battikh K, Drissa M, Kaabachi S, Najar T, Tlili R, Chahbani I, Charfeddine H, Ben MM, Braham S, Maatouk F, Abdesselem S, Ayari M, Garbaa R, Hamrouni N, Mbarek D, Rekik H, Zaghdoudi H, Ayadi W, Baraket F, Ben Brahim K, Ben Romdhane M, Bousadia H, Brahim W, Mezri M, Guesmi A, Ounissi T, Kammoun S, Smati W, Tlili S, Zoughi K, Zemni J, Cheikh Bouhlel M, Islem S, Jemli R, Joulak A, Mzoughi K, Naanea H, Hached L, Hadrich M, Hmem M, Kacem S, Kammoun I, Othmani R, Ouerghi A, Abid S, Ennouri R, Haidar S, Heraiech S, Jammali M, Jarrar M, Riahi L, Trimech B, Azaiez MA, Azzouzi F, Ben Jemaa K, Ben Rejab O, Chrigui R, Wechtati W, Boughzela E, Jridi G, Bezdah L, Kraiem S, Drissa H, Ben Youssef S, Fehri W, Kachboura S, Gamra H, Kammoun S, Mourali MS, Addad F, and Abid L
- Subjects
- Anticoagulants therapeutic use, Female, Humans, Male, Prospective Studies, Registries, Risk Factors, Tunisia epidemiology, Atrial Fibrillation diagnosis, Atrial Fibrillation drug therapy, Atrial Fibrillation epidemiology, Stroke
- Abstract
Background: Contemporary registries on atrial fibrillation (AF) are scare in North African countries., Hypothesis: In the context of the epidemiological transition, prevalence of valvular AF in Tunisia has decreased and the quality of management is still suboptimal., Methods: NATURE-AF is a prospective Tunisian registry, involving consecutive patients with AF from March 1, 2017 to May 31, 2017, with a one-year follow-up period. All the patients with an Electrocardiogram-documented AF, confirmed in the year prior to enrolment were eligible. The epidemiological characteristics and outcomes were described., Results: A total of 915 patients were included in this study, with a mean age of 64.3 ± 22 years and a male/female sex ratio of 0.93. Valvular AF was identified in 22.4% of the patients. The mean CHA
2 DS2 VASC score in nonvalvular AF was 2.4 ± 1.6. Monotherapy with antiplatelet agents was prescribed for 13.8% of the patients. However, 21.7% of the subjects did not receive any antithrombotic agent. Oral anticoagulants were prescribed for half of the patients with a low embolic risk score. In 341 patients, the mean time in therapeutic range was 48.87 ± 28.69%. Amiodarone was the most common antiarrhythmic agent used (52.6%). During a 12-month follow-up period, 15 patients (1.64%) had thromboembolism, 53 patients (5.8%) had major hemorrhage, and 52 patients (5.7%) died., Conclusions: NATURE-AF has provided systematic collection of contemporary data regarding the epidemiological and clinical characteristics as well as the management of AF by cardiologists in Tunisia. Valvular AF is still prevalent and the quality of anticoagulation was suboptimal., (© 2021 The Authors. Clinical Cardiology published by Wiley Periodicals LLC.)- Published
- 2021
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11. Epidemiology of thromboembolic and hemorrhagic events in patients with atrial fibrillation under anti-vitamin K.
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Ben Rejeb O, Brahim W, Ghali H, Ernez S, Mahdhaoui A, and Jeridi G
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- Adult, Aged, Aged, 80 and over, Anticoagulants therapeutic use, Female, Hemorrhage chemically induced, Humans, Incidence, Longitudinal Studies, Male, Middle Aged, Risk Factors, Stroke epidemiology, Thromboembolism prevention & control, Tunisia epidemiology, Vitamin K therapeutic use, 4-Hydroxycoumarins therapeutic use, Atrial Fibrillation drug therapy, Atrial Fibrillation epidemiology, Hemorrhage epidemiology, Indenes therapeutic use, Thromboembolism epidemiology, Vitamin K antagonists & inhibitors
- Abstract
Background: Atrial fibrillation is the most common heart rhythm disorder in the general population. It is associated with increased cardiovascular morbidity and mortality. Given this risk, anticoagulant therapy is vital., Aim: To estimate the incidence of thromboembolic and hemorrhagic events in patients with Atrial fibrillation and treated by oral anticoagulant in a cardiology department., Methods: We carried out an observational longitudinal study over a period of three years (January 2013 - December 2015) in the external consultation of cardiology of Farhat Hached hospital of Sousse. Pre-established individual records were used as a source and tool for data collection., Results: Overall, 200 patients were eligible. Forty-nine percent had valvular atrial fibrillation. After an average follow-up of 2.6 years, 15 thromboembolic events were noted affecting 13 patients (6.5%), with an incidence of 2.8%. We found a significant association between TTR <50% and the occurrence of stroke and transient ischemic events. Half of the patients had minor bleeding and 9.5% had major bleeding, with an incidence of 3.6%. No significant correlation between these accidents and the TTR was found. In addition, 9.5% of patients were hospitalized for international normalized ratio equilibration. They were mainly patients with valvular atrial fibrillation (72%) (p = 0.002)., Conclusion: Anticoagulant therapy with anti-vitamin-K remains the most adequate treatment. Thus, a well-conducted treatment ensures a reduction in thromboembolic risk and minimizes the occurrence of hemorrhages inherent to this therapy. Therefore, an assessment of the quality of anticoagulation is essential.
- Published
- 2019
12. Malignant pleural mesothelioma segmentation for photodynamic therapy planning.
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Brahim W, Mestiri M, Betrouni N, and Hamrouni K
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- Algorithms, Humans, Lung Neoplasms drug therapy, Mesothelioma drug therapy, Mesothelioma, Malignant, Lung Neoplasms diagnostic imaging, Mesothelioma diagnostic imaging, Patient Care Planning, Photochemotherapy, Thoracic Cavity diagnostic imaging, Tomography, X-Ray Computed methods
- Abstract
Medical imaging modalities such as computed tomography (CT) combined with computer-aided diagnostic processing have already become important part of clinical routine specially for pleural diseases. The segmentation of the thoracic cavity represents an extremely important task in medical imaging for different reasons. Multiple features can be extracted by analyzing the thoracic cavity space and these features are signs of pleural diseases including the malignant pleural mesothelioma (MPM) which is the main focus of our research. This paper presents a method that detects the MPM in the thoracic cavity and plans the photodynamic therapy in the preoperative phase. This is achieved by using a texture analysis of the MPM region combined with a thoracic cavity segmentation method. The algorithm to segment the thoracic cavity consists of multiple stages. First, the rib cage structure is segmented using various image processing techniques. We used the segmented rib cage to detect feature points which represent the thoracic cavity boundaries. Next, the proposed method segments the structures of the inner thoracic cage and fits 2D closed curves to the detected pleural cavity features in each slice. The missing bone structures are interpolated using a prior knowledge from manual segmentation performed by an expert. Next, the tumor region is segmented inside the thoracic cavity using a texture analysis approach. Finally, the contact surface between the tumor region and the thoracic cavity curves is reconstructed in order to plan the photodynamic therapy. Using the adjusted output of the thoracic cavity segmentation method and the MPM segmentation method, we evaluated the contact surface generated from these two steps by comparing it to the ground truth. For this evaluation, we used 10 CT scans with pathologically confirmed MPM at stages 1 and 2. We obtained a high similarity rate between the manually planned surface and our proposed method. The average value of Jaccard index was about 0.79 and we obtained a value of 0.88 using the Dice index., (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Published
- 2018
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13. Acute monocytic leukemia with coexpression of minor BCR-ABL1 and PICALM-MLLT10 fusion genes along with overexpression of HOXA9.
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Sindt A, Deau B, Brahim W, Staal A, Visanica S, Villarese P, Rault JP, Macintyre E, and Delabesse E
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- Adolescent, Bone Marrow metabolism, Follow-Up Studies, Fusion Proteins, bcr-abl genetics, Gene Fusion, Homeodomain Proteins genetics, Humans, In Situ Hybridization, Fluorescence, Karyotyping, Leukemia, Monocytic, Acute metabolism, Male, Metaphase, Models, Genetic, Monomeric Clathrin Assembly Proteins genetics, Monomeric Clathrin Assembly Proteins metabolism, Oncogene Proteins, Fusion genetics, Phenotype, Transcription Factors genetics, Transcription Factors metabolism, Translocation, Genetic, fms-Like Tyrosine Kinase 3 genetics, fms-Like Tyrosine Kinase 3 metabolism, Fusion Proteins, bcr-abl metabolism, Gene Expression Regulation, Neoplastic, Homeodomain Proteins metabolism, Leukemia, Monocytic, Acute genetics, Oncogene Proteins, Fusion metabolism
- Abstract
The t(9;22)(q34;q11) translocation occurs in chronic myeloid leukemia (CML) and adult B-cell acute lymphoblastic leukemia (ALL), leading to fusion of BCR to ABL1 and constitutive activation of ABL1 tyrosine kinase activity. The main BCR-ABL1 breakpoints result in P190 BCR-ABL1 or P210 BCR-ABL1 fusion proteins. The latter is found in almost all cases of CML and in one third of the cases of t(9;22)-positive adult B-ALL. P190 BCR-ABL1 is found in the remaining two thirds of t(9;22)-positive adult B-ALL cases but only exceptionally in CML. We describe here the first case of t(9;22)(q34;q11) associated with t(10;11)(p13;q14) in acute monocytic leukemia. The recurrent t(10;11)(p13;q14) translocation, usually found in acute myeloid leukemia (AML) and T-ALL, merges PICALM to MLLT10. RT-PCR enabled identification of PICALM-MLLT10 and BCR-ABL1 e1-a2 fusion transcripts; in the context of chronic and acute myeloid leukemia, the latter usually has a monocytic presentation. We also identified overexpression of HOXA9, a gene essential to myeloid differentiation that is expressed in PICALM-MLLT10 and MLL-rearranged acute leukemias. This case fits with and extends a recently proposed multistage AML model in which constitutive activation of tyrosine kinases by mutations (BCR-ABL1) are associated with deregulation of transcription factors central to myeloid differentiation (HOXA9 secondary to PICALM-MLLT10)., ((c) 2006 Wiley-Liss, Inc.)
- Published
- 2006
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14. AF4p12, a human homologue to the furry gene of Drosophila, as a novel MLL fusion partner.
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Hayette S, Cornillet-Lefebvre P, Tigaud I, Struski S, Forissier S, Berchet A, Doll D, Gillot L, Brahim W, Delabesse E, Magaud JP, and Rimokh R
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- Aged, Amino Acid Sequence, Animals, Artificial Gene Fusion, Base Sequence, Chromosomes, Human, Pair 11 genetics, Chromosomes, Human, Pair 4 genetics, DNA-Binding Proteins biosynthesis, Drosophila genetics, Female, Histone-Lysine N-Methyltransferase, Humans, Molecular Sequence Data, Myeloid-Lymphoid Leukemia Protein, Neoplasms, Second Primary genetics, Oncogene Proteins, Fusion biosynthesis, Protein Structure, Tertiary, RNA, Messenger biosynthesis, RNA, Messenger genetics, Recombinant Fusion Proteins biosynthesis, Recombinant Fusion Proteins genetics, Transcription Factors biosynthesis, Transcriptional Activation, Translocation, Genetic, DNA-Binding Proteins genetics, Oncogene Proteins, Fusion genetics, Precursor Cell Lymphoblastic Leukemia-Lymphoma genetics, Proto-Oncogenes genetics, Transcription Factors genetics
- Abstract
More than 35 different partner genes with the mixed lineage leukemia (MLL) gene have been cloned from leukemia cells with translocations involving chromosome 11 band q23. In this study, we report on a novel fusion partner of the MLL gene, AF4p12, which we have identified as the human homologue to the furry gene of Drosophila. AF4p12, highly conserved in evolution, encodes a large protein of 3,105 amino acids. The expression of AF4p12 has been preferentially detected in colon, placenta, and brain tissues and in tumor cells of lymphoid origin. We show that the t(4;11)(p12;q23) translocation results in the creation of a chimeric RNA encoding a putative fusion protein containing 1,362 amino acids from the NH2-terminal part of MLL and 712 amino acids from the COOH-terminal part of AF4p12. FLT3 and HOXA9 genes are overexpressed in this leukemia. We found that the COOH-terminal part of AF4p12 fused to MLL contains a leucine zipper motif and exhibits transcriptional activation properties when fused to Gal4 DNA-binding domains in transient transfection assays. The AF4p12 fragment fused to MLL may contribute to the oncogenic activation of MLL, possibly through specific recruitment of the transcriptional machinery.
- Published
- 2005
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15. [Laurence Moon Bardet Biedl syndrome: review of 2 familial cases].
- Author
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Jeddi A, M'Rabet A, Ruhaumoly Y, Soussi H, Ben Brahim W, Gharbi M, Soukeh M, el Kamel J, and Gaigi S
- Subjects
- Adolescent, Child, Consanguinity, Female, Humans, Male, Pedigree, Laurence-Moon Syndrome genetics
- Published
- 1997
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