Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Abdelkrim Boulanouar"'
Publikováno v:
Saudi Journal of Medical and Pharmaceutical Sciences. 6:466-469
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1acbc658160900c0983b5cbdf2bc5e5b
https://doi.org/10.36348/sjmps.2020.v06i06.010
https://doi.org/10.36348/sjmps.2020.v06i06.010
Publikováno v:
Saudi Journal of Medical and Pharmaceutical Sciences. 6:470-473
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::488aef7c48d88703a161986a5e1939be
https://doi.org/10.36348/sjmps.2020.v06i06.011
https://doi.org/10.36348/sjmps.2020.v06i06.011
Publikováno v:
Ophthalmology Journal. 5:146-149
Serpiginous-like choroiditis is a rare manifestation of intraocular tuberculosis. It most often occurs in the context of suspected or latent tuberculosis. The diagnostic confirmation remains a real challenge. We report a case of a young patient prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edce0f75bd2b71f489ca80de4dec3afa
https://doi.org/10.5603/oj.2020.0029
https://doi.org/10.5603/oj.2020.0029
Autor:
Yassamine Doubaj, Mustapha El Alloussi, Abdelali Zrhidri, Imane Cherkaoui Jaouad, Jaber Lyahyai, Abdelkrim Boulanouar, Soukaina Guaoua, Abdelaziz Sefiani
Publikováno v:
European Journal of Medical Genetics. 60:239-244
Jalili syndrome is a rare autosomal recessive genetic disease characterized by the association of amelogenesis imperfecta and cone-rod retinal dystrophy. This syndrome is caused by mutations in the CNNM4 gene. Different types of CNNM4 mutations have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7eba4baefee0b2190c15fdc0ca5e3f4
https://doi.org/10.1016/j.ejmg.2017.02.004
https://doi.org/10.1016/j.ejmg.2017.02.004