Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mouhamed Eleuch"'
Autor:
Yasmine Makhlouf, Soumaya Boussaid, Houda Ajlani, Samia Jemmali, Sonia Rekik, Hela Sehli, Mouhamed Eleuch
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
Background: Neurofibromatosis type 1 (NF1), also known as von Recklinghausen disease, is a one of the more common hereditary autosomal disorders. However, osteomalacia in neurofibromatosis type 1 is very rare tumour-induced osteomalacia; fibroblast g
Externí odkaz:
https://doaj.org/article/128fd9911e214a8d90090c7313e6939c
Autor:
S. Jemmali, Hela Sehli, Soumaya Boussaid, Mouhamed Eleuch, Yasmine Makhlouf, H. Ajlani, Sonia Rekik
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
Background Neurofibromatosis type 1 (NF1), also known as von Recklinghausen disease, is a one of the more common hereditary autosomal disorders. However, osteomalacia in neurofibromatosis type 1 is very rare tumour-induced osteomalacia; fibroblast gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c829c91a7b0f5914f1140d4e68bf9531
https://doi.org/10.12890/2021_002618
https://doi.org/10.12890/2021_002618