Zobrazeno 1 - 10 of 100 pro vyhledávání: '"S, Mseddi"'
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A COMBINED ELECTROCOAGULATION-ELECTROOXIDATION TREATMENT FOR DAIRY WASTEWATER
Autor: C. Belaid, M. Kallel, L. Chaari, S. Mseddi, I. Chakchouk, N. Elloumi
Publikováno v: Brazilian Journal of Chemical Engineering v.34 n.1 2017
Brazilian Journal of Chemical Engineering
Associação Brasileira de Engenharia Química (ABEQ)
instacron:ABEQ
Brazilian Journal of Chemical Engineering, Volume: 34, Issue: 1, Pages: 109-117, Published: JAN 2017
Brazilian Journal of Chemical Engineering, Vol 34, Iss 1, Pp 109-117
Dairy industry effluent is characterized by high chemical oxygen demand (COD) and other pollution load. This study addresses the elimination of organic compounds in dairy wastewater using electrocoagulation (EC), electrooxidation (EO) and a synergist
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::296193fd56df5b1a9741fe0fa30f25fc
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322017000100109
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Akademický článek
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Gammapathies monoclonales en Tunisie : analyse épidémiologique, immunochimique et étiologique d'une série de 288 cas
Autor: M.S. Krichen, J. Hachicha, Hatem Masmoudi, M. Ben Ayed, Zouhir Bahloul, S. Mseddi-Hdiji, S. Baklouti, M. Elloumi, S. Haddouk, Nabil Tahri
Publikováno v: Pathologie Biologie. 53:19-25
From July 1992 to December 2000, 288 cases of monoclonal gammapathy (MG) were collected at the university hospital of Sfax. The middle age of the patients at the time of the diagnosis was 62 years and 7 months with extremes to 18 months and 99 years
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::428ebbc2490daf6536651922c2a8c667
https://doi.org/10.1016/j.patbio.2004.01.014
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6
La maladie de Fanconi: étude de 43 cas dans le sud tunisien
Autor: Afef Khanfir, A. Saad, T. Souissi, S Mseddi, M. Elloumi, J. Mnif, M. Bouaziz, Mounir Frikha
Publikováno v: Archives de Pédiatrie. 5:1200-1205
Resume Objectifs . — Degager les aspects epidemiologiques, cliniques, biologiques et evolutifs de la maladie de Fanconi dans le sud tunisien. Patients et methodes . — Nous avons collige 43 cas sur une periode de 12 ans. Pour chaque malade ont ete
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::64249bb926d8552eff799df041361d75
https://doi.org/10.1016/s0929-693x(98)81232-3
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Primary Plasmacytoma of The Testis with no Evidence of Multiple Myeloma: a New Case Report and Literature Review
Autor: Ali Bahloul, J. Daoud, S. Mseddi-Hdiji, H. Ketata, S. Makni, Mohamed Nabil Mhiri, Mehdi Bouassida
Publikováno v: African Journal of Urology; Vol 16, No 3 (2010)
Plasmacytomas of the testis are extremely rare tumours, especially when occurring in the absence of a previous or concurrent diagnosis of multiple myeloma. We report a new case of solitary testicular plasmacytoma, with immunohistochemical studies sho
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57b3c4889b96ebfe7f04e4475bfb37d7
https://www.ajol.info/index.php/aju/article/view/63621
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8
[Nosologic discussion between Fanconi disease and congenital dyskeratosis: 1 case of congenital bone marrow aplasia]
Autor: S, Mseddi, N, Ben Aribia, R, Horchani, M, Elloumi, H, Elghezal, T, Souissi
Publikováno v: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 13(9)
Based on a case report of aplastic anemia associated with malformation, we discuss the diagnostic criteria and the nosologic problem between the 2 principal aplastic anemia accompanied with malformation: Fanconi disease and dyskeratosis congenita.A 1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fd84cb49ab7ffc9e47fb15c7634491cc
https://pubmed.ncbi.nlm.nih.gov/16854573
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9
[Congenital factor XIII deficiency in the south of Tunisia]
Autor: M, Medhaffar, M, Elloumi, S, Guermazi, C, Kallel, S, Mseddi, H, Bellaaj, F, Makni, T, Souissi
Publikováno v: Pathologie-biologie. 54(6)
Factor XIII deficiency is a rare autosomal recessive congenital disorder of haemostasis characterised by a plasmatic factor XIII level less than 1% in homozygote and bleeding as of the youth. We report a study about ten patients with congenital facto
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d0e8118359ec4199083824f45306b6c2
https://pubmed.ncbi.nlm.nih.gov/16530351
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10
[Plasmocytic pleural effusion disclosing multiple myeloma]
Autor: M, Elloumi, M, Frikha, H, Masmoudi, S, Mseddi, M, Ben Ayed, M, Bouaziz, F, Makni, T, Souissi
Publikováno v: Revue des maladies respiratoires. 17(2)
Pleural effusion caused by plasma cell involvement in multiple myeloma has been reported unfrequently, and has been described at a frequency below 1% of multiple myeloma. In this study, we report an observation with pleural effusion as first symptom
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::99ec82efbf7c6e38a8a25204ad5534ed
https://pubmed.ncbi.nlm.nih.gov/10859769
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