Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Leila Elmatri"'
Autor:
Zied Riahi, Crystel Bonnet, Rim Zainine, Saida Lahbib, Yosra Bouyacoub, Rym Bechraoui, Jihène Marrakchi, Jean-Pierre Hardelin, Malek Louha, Leila Largueche, Salim Ben Yahia, Moncef Kheirallah, Leila Elmatri, Ghazi Besbes, Sonia Abdelhak, Christine Petit
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0120584 (2015)
Usher syndrome (USH) is an autosomal recessive disorder characterized by combined deafness-blindness. It accounts for about 50% of all hereditary deafness blindness cases. Three clinical subtypes (USH1, USH2, and USH3) are described, of which USH1 is
Externí odkaz:
https://doaj.org/article/a1cec40889d2405db2ba7c181f4782b6
Autor:
Sonia Abdelhak, Zied Riahi, L. Largueche, Rim Zainine, Moncef Kheirallah, Leila Elmatri, Christine Petit, Ghazi Besbes, Saida Lahbib, Yosra Bouyacoub, J. Marrakchi, Crystel Bonnet, Jean-Pierre Hardelin, Salim Ben Yahia, Rym Bechraoui, Malek Louha
Publikováno v:
PLoS ONE
PLoS ONE, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
PLoS ONE, Public Library of Science, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
PLoS ONE, Vol 10, Iss 3, p e0120584 (2015)
PLoS ONE, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
PLoS ONE, Public Library of Science, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
PLoS ONE, Vol 10, Iss 3, p e0120584 (2015)
International audience; Usher syndrome (USH) is an autosomal recessive disorder characterized by combined deafness-blindness. It accounts for about 50% of all hereditary deafness blindness cases. Three clinical subtypes (USH1, USH2, and USH3) are des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49896b9629524498a57fde1557d4de8a
https://hal-pasteur.archives-ouvertes.fr/pasteur-01221041/document
https://hal-pasteur.archives-ouvertes.fr/pasteur-01221041/document
Autor:
Mbarka Bchetnia, Selma Kassar, A. Merdassi, Fatma Mgaieth, Mourad Mokni, Amel Dhahri-Ben Osman, Hamouda Boussen, Sonia Abdelhak, M.S. Boubaker, Cherine Charfeddine, Leila Elmatri, I. Chouchene, Farah Ouechtati
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 4, Iss 1, p 108 (2010)
Journal of Medical Case Reports, Vol 4, Iss 1, p 108 (2010)
Introduction Mal de Meleda is a rare form of palmoplantar keratoderma, with autosomal recessive transmission. It is characterized by diffuse erythema and hyperkeratosis of the palms and soles. Recently, mutations in the ARS (component B) gene (ARS, M
Autor:
Hela Rifi, Bassem Allani, Sarra Krimi, Mouna Ayadi, Aymen Lagha, Amel Mezlini, Leila Elmatri, L. Largueche, Henda Raies, Nesrine Chraiet
Publikováno v:
International Journal of Case Reports and Images. 3:6
Introduction: To present a case of chemotherapeutic regression of metastasis of breast carcinoma to the choroid in a male patient. Case Report: A 63-year-old male, with a past medical history of breast cancer, presented with blurred vision and progre