Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mehdi Elfakiri"'
Autor:
Youssef Lakhdar, Hind Abou El Houda, Houda Mounji, Mehdi Elfakiri, Youssef Rochdi, Abdeljalil Moutaouakil, Abdelaziz Raji
Publikováno v:
The Egyptian Journal of Otolaryngology, Vol 37, Iss 1, Pp 1-5 (2021)
Abstract Background Tietz syndrome is a very rare clinical entity characterized by the association of profound bilateral congenital sensorineural deafness and generalized hypopigmentation of skin, eyes, and integuments (snow white appearance). It is
Externí odkaz:
https://doaj.org/article/a94f062046664cc5875043d58829ca9b
Autor:
Mehdi Elfakiri, Abdelaziz Raji, Hind Abou El Houda, Youssef Rochdi, Youssef Lakhdar, Abdeljalil Moutaouakil, Houda Mounji
Publikováno v:
The Egyptian Journal of Otolaryngology, Vol 37, Iss 1, Pp 1-5 (2021)
Background Tietz syndrome is a very rare clinical entity characterized by the association of profound bilateral congenital sensorineural deafness and generalized hypopigmentation of skin, eyes, and integuments (snow white appearance). It is an autoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ffc60265038be25eff4b757208fd4e0
https://doaj.org/article/a94f062046664cc5875043d58829ca9b
https://doaj.org/article/a94f062046664cc5875043d58829ca9b
Publikováno v:
Journal of Novel Physiotherapy and Rehabilitation. 3:082-089
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::611468efafec8a3d1087bcbd315d76bb
https://doi.org/10.29328/journal.jnpr.1001028
https://doi.org/10.29328/journal.jnpr.1001028
Autor:
Houda, Mounji, Salk, Eddafi, Malika, Benfdil, Mehdi, Elfakiri, Youssef, Rochdi, Hassan, Nouri, Abdelaziz, Raji
Publikováno v:
Pan African Medical Journal; Sep-Dec2020, Vol. 37, p1-6, 6p
Autor:
Raji, Abdelaziz1 (AUTHOR), Mounji, Houda1 (AUTHOR), Chehbouni, Mohammed1 (AUTHOR), Rochdi, Youssef1 (AUTHOR), Nouri, Hassan1 (AUTHOR), Elfakiri, Mehdi1 (AUTHOR)
Publikováno v:
Indian Journal of Otology. Jul-Sep2021, Vol. 27 Issue 3, p148-152. 5p.