Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Jalel, Chemli"'
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-5 (2023)
Abstract Background Patients with Down syndrome are at a higher risk of developing autoimmune disorders such as thyroiditis, diabetes, and celiac disease compared with the general population. Although some diseases are well known to be associated wit
Externí odkaz:
https://doaj.org/article/e747a058e9d94b7196f2ec19c8b841db
Autor:
Houda Ajmi, Jawher Brahim, Sameh Mabrouk, Amel Ben Abdallah, Noura Zouari, Fadoua Majdoub, Salsabil Nouir, Ibtissem Hasni, Yasser Ben Cheikh, Jalel Chemli, Hela Jemni, Saoussan Abroug
Publikováno v:
European Journal of Paediatric Neurology. 43:18-26
Autor:
N. Zouari, H. Ajmi, Saoussen Abroug, Najoua Kahloul, Sameh Mabrouk, Sameh Ghorbel, Jalel Chemli, Lamia Boughammoura, Kais Mansour, Houssin Mejaouel, Olfa Ezzi
Publikováno v:
Annales de Cardiologie et d'Angéiologie. 71:86-89
Introduction Kawasaki syndrome (KS) is a systemic vasculitis of unknown etiology that affects medium and small blood vessels. The aim of our study is to analyze coronary artery lesions in children with KS and their risk factors. Material and methods
Autor:
Houda Ajmi, Fadoua Majdoub, Mehdi Gaha, Jalel Chemli, Noura Zouari, Hela Jemni, Saida Hassayoun, Saoussan Abroug
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 7, Iss 2, Pp e070239-e070239 (2018)
Neonatal and pediatric heart failure is commonly caused by congenital heart diseases, especially by large left-to-right shunting. It is rarely related to a Vein of Galen Aneurysmal Malformation (VGAM). Diagnosis and management of these cerebrovascula
Externí odkaz:
https://doaj.org/article/1fc7e06a61ad43c980015537695227fd
Autor:
Jalel Chemli, Nadia Mama, S. Abroug, N. Arifa, Nesrine Jammeli, N. Zouari, H. Jemni, H. Ajmi, Sameh Mabrouk, S. Hassayoun
Publikováno v:
Archives de Pédiatrie. 28:638-646
Background Acute disseminated encephalomyelitis (ADEM) is an inflammatory demyelinating disorder of the central nervous system. Little information is available about the clinical and neuroradiological profile or the follow-up of this disease in Tunis
Autor:
Houda, Ajmi, Sameh, Ghorbel, Olfa, Ezzi, Sameh, Mabrouk, Kais, Mansour, Najoua, Kahloul, Jalel, Chemli, Noura, Zouari, Houssin, Mejaouel, Lamia, Boughammoura, Saoussen, Abroug
Publikováno v:
Annales de cardiologie et d'angeiologie. 71(2)
Kawasaki syndrome (KS) is a systemic vasculitis of unknown etiology that affects medium and small blood vessels. The aim of our study is to analyze coronary artery lesions in children with KS and their risk factors.All children under the age of 15 ye
Publikováno v:
World Journal of Clinical Cases
Pseudotumoral cerebellitis in childhood is an uncommon presentation of cerebellitis mimicking a brain tumor. It often follows an inflammatory or infectious event, particularly due to varicella virus. Patients could have a wide clinical spectrum on pr
Autor:
Hayet Kaarout, Jalel Chemli, Abdellatif Achour, Amira Moussa, Asma Omezzine, Saoussen Abroug, Ali Bouslama, Geneviéve Souche, Sabra Aloui, Saoussen M'dimegh, Ibtihel M'barek, Cécile Aquaviva-bourdain, Sameh Mabrouk
Publikováno v:
Annals of Human Genetics. 81:1-10
Background Primary hyperoxaluria type 1 (PH1) is an autosomal recessive metabolic disorder caused by inherited mutations in the AGXT gene encoding liver peroxisomal alanine:glyoxylate aminotransferase (AGT). PH1 is a clinically and genetically hetero
Autor:
Khaoula Ben-Farhat, Monia Khemiri, Zohra Fitouri, Sihem Barsaoui, Najla Mekki, Meriem Ben-Ali, Selim Abdelmoula, Mohamed-Neji Guediche, M. R. Barbouche, Samir Boukthir, Saber Hamami, Imen Ben-Mustapha, Amel Ben-Chehida, Jalel Chemli, Karen Rouault, Beya Larguèche
Publikováno v:
Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2016, 36 (6), pp.547-554. ⟨10.1007/s10875-016-0299-9⟩
Journal of Clinical Immunology, Springer Verlag, 2016, 36 (6), pp.547-554. ⟨10.1007/s10875-016-0299-9⟩
International audience; Chronic granulomatous disease (CGD) is the prototypic functional neutrophil disorder caused by genetic defects in one of the five genes encoding the superoxide-generating nicotinamide adenine dinucleotide phosphate (NADPH)-oxi
Autor:
Lamia Boughammoura, T. Sfar, Meriem Ben Ali, S. Hassayoun, J. Bouguila, Jalel Chemli, Fethi Bayoudh, Raoudha Boussoffara, Abdelmajid Mahfoudh, Imen Chabchoub, Abdelaziz Harbi, Najla Mekki, Agnes Hamzaoui, Imen Ben Mustapha, Fethi Mellouli, A. Bouaziz, Beya Larguèche, F. Amri, Zakia Habboul, Mohamed-Ridha Barbouche, Saida Ben Becher, Neji Tebib, Habib Besbes, Siheme Barsaoui, N. Gueddiche, Jamel Ammar, Monia Ben Khaled, Mongia Hachicha, Monia Ouederni, Lamia Ben Mansour, Azza Sammoud, Najla Ben Jaballah, Najoua Guandoura, Hajer Aloulou, A. Meherzi, Khadija Boussetta, Mohamed Bejaoui, Saber Hammami
Publikováno v:
Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2015, 35 (8), pp.745-753. ⟨10.1007/s10875-015-0206-9⟩
Journal of Clinical Immunology, Springer Verlag, 2015, 35 (8), pp.745-753. ⟨10.1007/s10875-015-0206-9⟩
International audience; Primary immunodeficiencies (PIDs) are a large group of diseases characterized by susceptibility to not only recurrent infections but also autoimmune diseases and malignancies. The aim of this study was to describe and analyze