Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Wissem Ben Azzouz"'
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:
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