Zobrazeno 1 - 10 of 17 pro vyhledávání: '"Bayen, Maalej"'
1
Akademický článek
Lupus Nephritis in Tunisian Children: Predictive Factors of Poor Outcomes
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
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2
Akademický článek
Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations
Autor: Houda Kanoun, Faiçal Jarraya, Bayen Maalej, Amina Lahiani, Hichem Mahfoudh, Fatma Makni, Jamil Hachicha, Faiza Fakhfakh
Publikováno v: BMC Nephrology, Vol 18, Iss 1, Pp 1-10 (2017)
Abstract Background Primary hyperoxaluria type 1 (PH1) is an autosomal recessive inherited disorder of glyoxylate metabolism in which excessive oxalates are formed by the liver and excreted by the kidneys. Calcium oxalate crystallizes in the urine, l
Externí odkaz: https://doaj.org/article/01c505f1ebc94f27b43724793dc95d09
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3
Akademický článek
An unusual case of pediatric acute nicotine poisoning due to a dermal exposure
Autor: Manel Weli, Mouna Jerbi, Olfa Chakroun-Walha, Bayen Maalej, Lamia Gargouri, Noureddine Rekik, Abdelmajid Mahfoudh
Publikováno v: Journal of Acute Disease, Vol 8, Iss 1, Pp 41-42 (2019)
Acute intoxication with nicotine is possible to cause nonspecific clinical signs and may be serious and lead to the death. We report a rare and severe form of acute nicotine poisoning secondary to dermal absorption of tobacco.
Externí odkaz: https://doaj.org/article/51734e6537f54f949f8d355fa0f177d5
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4
Next-generation sequencing in patients with familial FSGS: first report of collagen gene mutations in Tunisian patients
Autor: Elisabet Ars, Patricia Ruiz, Andrea Domingo-Gallego, T. Boudawara, Bayen Maalej, Laura Lorente-Grandoso, Faical Jarraya, Sawssan Ammar, Khawla Kammoun, Hassen Kamoun, Mohamed Ben Hmida, Marc Pybus, Houda Kanoun
Publikováno v: JOURNAL OF HUMAN GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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Focal segmental glomerulosclerosis (FSGS) is a histological lesion with many causes, including inherited genetic defects, with significant proteinuria being the predominant clinical finding at presentation. FSGS is considered as a podocyte disease du
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c20f49bb265b60bd4620d9ffa17a87d
https://doi.org/10.1038/s10038-021-00912-2
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5
La glomérulonéphrite aiguë post-streptococcique de l’enfant dans le sud tunisien : étude rétrospective de 12 ans
Autor: Taher Gargah, Bayen Maalej, Manel Weli, Manel Jallouli, Khaoula Kamoun, Mohamed Charfi, Jamil Hachicha, Mona Ben Amor, Olfa Chakroun, Lamia Gargouri, Yassine Abdelkefi, Noureddine Rekik, Abdelmajid Mahfoudh
Publikováno v: Néphrologie & Thérapeutique. 14:518-522
Resume Introduction La glomerulonephrite aigue (GNA) post-streptococcique est une cause frequente de glomerulonephrite aigue chez l’enfant. L’objectif de ce travail etait de decrire les particularites cliniques et evolutives et de chercher des fa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ca6e466296ba8dfdfd88b45ed1fe3267
https://doi.org/10.1016/j.nephro.2018.04.001
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6
P660 Abscess of the kidney, a diagnosis not always evident!
Autor: Manel Hsairi, Faiza Safi, Abdelmajid Mahfoudh, Chiraz Regaieg, Lamia Gargouri, Bayen Maalej
Publikováno v: Abstracts.
Introduction Kidney abscess is defined as a suppurate lesion collected in the renal parenchyma. It is a rare pathology in pediatrics. We report four cases of renal suppuration. Material and method This is a retrospective study over a period of 9 year
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cb714652520a0877c3e51f8f1e33e88a
https://doi.org/10.1136/archdischild-2019-epa.990
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7
Épidémiologie de l’insuffisance rénale terminale de l’enfant en Tunisie
Autor: Tahar Gargah, Chokri Zarrouk, Manel Jellouli, Kamel Abidi, Abir Boussetta, O. Naija, Yousra Hammi, Abdelmajid Mahfoudh, Bayen Maalej
Publikováno v: Néphrologie & Thérapeutique. 12:166-170
Resume Introduction L’insuffisance renale chronique terminale (IRCT) chez l’enfant presente des particularites en termes d’etiologies, de modalites therapeutiques de suppleance et d’acces a la transplantation renale. Le but de notre etude eta
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dbc0605c7d4b2cc04ba2f1c32f9de781
https://doi.org/10.1016/j.nephro.2015.09.001
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8
[Post-streptococcal glomerulonephritis in the south of Tunisia: A 12-year retrospective review]
Autor: Bayen, Maalej, Mona, Ben Amor, Manel, Jallouli, Manel, Weli, Mohamed, Charfi, Yassine, Abdelkefi, Olfa, Chakroun, Khaoula, Kamoun, Jamil, Hachicha, Noureddine, Rekik, Taher, Gargah, Lamia, Gargouri, Abdelmajid, Mahfoudh
Publikováno v: Nephrologietherapeutique. 14(7)
Post-streptococcal glomerulonephritis (PSGN) is a frequent cause of acute nephritis in children. This study aimed to describe the epidemiology, clinical characteristics and outcomes of PSGN and look for predictor's factors of severity.A 12-year retro
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f92d80e758ca35b15beb1aef0c0aeba0
https://pubmed.ncbi.nlm.nih.gov/29735420
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9
Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations
Autor: Hichem Mahfoudh, Amina Lahiani, Houda Kanoun, Faical Jarraya, Faiza Fakhfakh, Fatma Makni, Bayen Maalej, Jamil Hachicha
Publikováno v: BMC Nephrology
BMC Nephrology, Vol 18, Iss 1, Pp 1-10 (2017)
Background Primary hyperoxaluria type 1 (PH1) is an autosomal recessive inherited disorder of glyoxylate metabolism in which excessive oxalates are formed by the liver and excreted by the kidneys. Calcium oxalate crystallizes in the urine, leading to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::847cb6b0ccd8f204809bee72a0975982
http://europepmc.org/articles/PMC5625645
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10
Rituximab in The Management of Pediatric Steroid-Resistant Nephrotic Syndrome: A Systematic Review
Autor: Bayen Maalej, Rim Charfi, Tahar Gargah, Manel Jellouli, Abdelmajid Mahfoud, Sameh Trabelsi
Publikováno v: The Journal of pediatrics. 197
Objectives To evaluate the efficacy and safety of rituximab in children with steroid-resistant nephrotic syndrome. Study design A systematic review evaluating the efficacy and safety of rituximab in children with steroid-resistant nephrotic syndrome
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d6c42a8d7dfc2684936513c44de0b45
https://pubmed.ncbi.nlm.nih.gov/29680473
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