Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Manal Alkhonezan"'
Publikováno v:
Clinical Case Reports, Vol 12, Iss 11, Pp n/a-n/a (2024)
Key clinical message Perrault syndrome (PRLTS) is an uncommon hereditary condition distinguished by ovarian failure in females and sensorineural hearing loss. Infertility can be the presenting problem for a serious disease. History and physical exami
Externí odkaz:
https://doaj.org/article/16e56d1399f44acab3eeb6511914f04c
Autor:
Ashjan Alheggi, Raneem Alnutaifi, Manal Alkhonezan, Norah Almudawi, Renad Alsuhaibani, Philip Moons, Turki Aljuhani
Publikováno v:
Dermatology Reports (2023)
Pruritus is one of the most debilitating symptoms for patients with epidermolysis bullosa (EB). This study aimed to assess the burden of itch and to address its dimensions across patients with EB. Forty-six patients with EB were recruited from the Sa
Externí odkaz:
https://doaj.org/article/c7468a1d623e4181ac4c743a953446c6
Autor:
Osamah Ahmad Hakami, Refah Asheer Alsubaie, Bayan Abdulhadi Albaqami, Haifa Matar Almutlaq, Nourah Mushabab Alqahtani, Manal Alkhonezan, Farah Fahad Almuqrin, Abdullah Hussien Alghamdi, Abdullah Abdulaziz Alaryni, Rayan Abubakker Qutob
Publikováno v:
Journal of Multidisciplinary Healthcare. 16:763-771
Osamah Ahmad Hakami,* Refah Asheer Alsubaie,* Bayan Abdulhadi Albaqami, Haifa Matar Almutlaq, Nourah Mushabab Alqahtani, Manal Alkhonezan, Farah Fahad Almuqrin, Abdullah Hussien Alghamdi, Abdullah Abdulaziz Alaryni, Rayan Abubakker Qutob Facu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6dd483591ffe05f8a310498a510339b
https://doi.org/10.2147/jmdh.s403999
https://doi.org/10.2147/jmdh.s403999