Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Sameh, Mabrouk"'
Autor:
Latifa Chkioua, Yessine Amri, Chaima Saheli, Wassila Mili, Sameh Mabrouk, Imen Chabchoub, Hela Boudabous, Wissem Ben Azzouz, Hadhami Ben Turkia, Salima Ferchichi, Neji Tebib, Taieb Massoud, Mohamed Ghorbel, Sandrine Laradi
Publikováno v:
Diagnostic Pathology, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Background Ocular cystinosis is a rare autosomal recessive disorder characterized by intralysosomal cystine accumulation in renal, ophthalmic (cornea, conjunctiva), and other organ abnormalities. Patients with ocular cystinosis are mostly as
Externí odkaz:
https://doaj.org/article/719f2484eacd45bd80f7b8a19e31bbfd
Autor:
Abir Boussetta, Dalia Louati, Manel Jellouli, Hanen Gaied, Sameh Mabrouk, Bayen Maalej, Karim Zouaghi, Rym Goucha, Tahar Gargah
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 33, Iss 3, Pp 440-448 (2022)
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disorder of unknown etiology. Lupus nephritis (LN) is one of the most severe clinical manifestations observed in patients with SLE; it is more frequent and more severe in children than in
Externí odkaz:
https://doaj.org/article/4c433c06bae6402bb58442581a8ee629
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:
Houda Ajmi, Sameh Mabrouk, Saida Hassayoun, Haifa Regaieg, Minyar Tfifha, Chemli Jalel, Hadef Skouri, Noura Zouari, Saoussan Abroug
Publikováno v:
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-4 (2017)
Abstract Background Autoimmune hemolytic anemia is rare in children. First-line therapies for this disease consist of corticosteroids and intravenously administered immunoglobulin that are effective in most patients. However, a small proportion of ca
Externí odkaz:
https://doaj.org/article/ec4692080df84e71b63b6c68d36b3391
Autor:
Neveen A Soliman, Sameh Mabrouk
Publikováno v:
Clinical Kidney Journal. 15:i33-i36
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive inborn error of metabolism characterized by marked hepatic overproduction of oxalate due to deficiency of hepatic peroxisomal alanine-glyoxylate aminotransferase caused by AGXT gene mutatio
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, Ines Trabelsi, Khouloud Rjiba, Sameh Mabrouk, Noura Zouari, Soumaya Mougou-Zerelli, Alain Verloes, Saoussan Abroug
Publikováno v:
Clinical Dysmorphology.
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:
Latifa Chkioua, Hadhami Ben Turkia, Chayma Saheli, Hela Boudabous, Imen Chabchoub, Sameh Mabrouk, Taieb Massoud, Mohamed Ghorbel, Wissem Ben Azzouz, Sandrine Laradi, Neji Tebib, Wassila Mili, Salima Ferchichi, Yessine Amri
Background: Ocular cystinosis is a rare autosomal recessive disorder characterized by intralysosomal cystine accumulation in renal, ophthalmic (cornea, conjunctiva), and other organ abnormalities. Patients with ocular cystinosis are mostly asymptomat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0152e7ff4c46bee6e0d47d342ec6076a
https://doi.org/10.21203/rs.3.rs-1027134/v1
https://doi.org/10.21203/rs.3.rs-1027134/v1
Autor:
Latifa Chkioua, Imen Chabchoub, Wissem Ben Azzouz, Mohamed Ghorbel, Neji Tebib, Salima Ferchichi, Chayma Saheli, Taieb Massoud, Hadhami Ben Turkia, Yessine Amri, Sandrine Laradi, Wassila Mili, Sameh Mabrouk, Hela Boudabous
Background: Ocular cystinosis is a rare autosomal recessive disorder characterized by intralysosomal cystine accumulation in renal, ophthalmic (cornea, conjunctiva), and other organ abnormalities. Patients with ocular cystinosis are mostly asymptomat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dd4d1baabf7f1eda2c8a552cccdc621
https://doi.org/10.21203/rs.3.rs-933169/v1
https://doi.org/10.21203/rs.3.rs-933169/v1