Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Chahed HE"'
Autor:
Hrira Mohamed Yahia, Chkioua Latifa, Slimani Afef, Chahed Henda, Mosbah Habib, Khaldoun Hamda Ben, Ferchichi Salima, Addad Faouzi, Miled Abdelhedi
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 88 (2012)
Abstract Coronary artery disease (CAD) is a multifactorial disease where genetic and environmental factors interact in complex ways to cause the disease. Heat shock protein genes are involved in the progress of CAD. This implies that genetic variants
Externí odkaz:
https://doaj.org/article/573ee2f181d6447a819751b263eb4c8f
Autor:
Chkioua Latifa, Khedhiri Souhir, Ben Turkia Hadhami, Chahed Henda, Ferchichi Salima, Ben Dridi Marie, Laradi Sandrine, Miled Abdelhedi
Publikováno v:
Diagnostic Pathology, Vol 6, Iss 1, p 113 (2011)
Abstract Mucopolysaccharidosis type I (MPS I) was a group of rare autosomal recessive disorder caused by the deficiency of the lysosomal enzyme, alpha -L -iduronidase, and the resulting accumulation of undergraded dematan sulfate and heparan sulfate.
Externí odkaz:
https://doaj.org/article/035771bee3a146f1859c01b6ce4a7c6d
Autor:
Chahed Henda, Froissart Roseline, Tcheng Rémy, Turkia Hadhami, Khedhiri Souhir, Chkioua Latifa, Ferchichi Salima, Ben Dridi Marie, Vianey-Saban Christine, Laradi Sandrine, Miled Abdelhedi
Publikováno v:
Diagnostic Pathology, Vol 6, Iss 1, p 47 (2011)
Abstract Background Mucopolysaccharidosis type I (MPS I) is an autosomal storage disease resulting from defective activity of the enzyme α-L-iduronidase (IDUA). This glycosidase is involved in the degradation of heparan sulfate and dermatan sulfate.
Externí odkaz:
https://doaj.org/article/07e4598581ac428d9abf4fd54b6bbb04
Autor:
Chkioua Latifa, Khedhiri Souhir, Ferchichi Salima, Tcheng Rémy, Chahed Henda, Froissart Roseline, Vianey-Saban Christine, Laradi Sandrine, Miled Abdelhedi
Publikováno v:
Diagnostic Pathology, Vol 6, Iss 1, p 42 (2011)
Abstract Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is X-linked recessive lysosomal storage disorder resulting from the defective activity of the enzyme iduronate-2-sulfatase (IDS). Hunter disease can vary from mild to severe, depending
Externí odkaz:
https://doaj.org/article/26eca73ad25644979dffd9c59ff39a6c
Autor:
Gharbi MA; Department of Orthopedic and Trauma Surgery Mongi Slim Marsa University Hospital Center Tunis Tunisia.; Faculty of Medicine of Tunis University of Tunis El Manar Tunis Tunisia., Chahed HE; Department of Orthopedic and Trauma Surgery Mongi Slim Marsa University Hospital Center Tunis Tunisia.; Faculty of Medicine of Tunis University of Tunis El Manar Tunis Tunisia., Slama SB; Faculty of Medicine of Tunis University of Tunis El Manar Tunis Tunisia.; Department of Anatomical Pathology Mongi Slim Marsa University Hospital Center Tunis Tunisia., Teborbi A; Department of Orthopedic and Trauma Surgery Mongi Slim Marsa University Hospital Center Tunis Tunisia.; Faculty of Medicine of Tunis University of Tunis El Manar Tunis Tunisia., Bouzidi R; Department of Orthopedic and Trauma Surgery Mongi Slim Marsa University Hospital Center Tunis Tunisia.; Faculty of Medicine of Tunis University of Tunis El Manar Tunis Tunisia., Nefiss M; Department of Orthopedic and Trauma Surgery Mongi Slim Marsa University Hospital Center Tunis Tunisia.; Faculty of Medicine of Tunis University of Tunis El Manar Tunis Tunisia.
Publikováno v:
Clinical case reports [Clin Case Rep] 2023 Nov 15; Vol. 11 (11), pp. e8170. Date of Electronic Publication: 2023 Nov 15 (Print Publication: 2023).