Zobrazeno 1 - 10
of 66
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, 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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3900efcdfd9a34b322da5ce4815584b
https://doi.org/10.1016/j.ancard.2021.10.011
https://doi.org/10.1016/j.ancard.2021.10.011
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6883f69f35291c2fb02429b0d0a77e16
https://doi.org/10.1016/j.arcped.2021.09.027
https://doi.org/10.1016/j.arcped.2021.09.027
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f41b79c941e681d3732980f1b9334a2
http://europepmc.org/articles/PMC5561503
http://europepmc.org/articles/PMC5561503
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff396de0b8279edb0a1bca82e8aed24b
https://doi.org/10.1111/ahg.12178
https://doi.org/10.1111/ahg.12178
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d93add6bc9843dc959ccce1265808deb
https://doi.org/10.1007/s10875-016-0299-9
https://doi.org/10.1007/s10875-016-0299-9
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