Zobrazeno 1 - 10
of 7 795
pro vyhledávání: '"A, Ben Salah"'
Autor:
Anis Jellad, Amine Kalai, Amr Chaabeni, Cyrine Ben Nasrallah, Atef Ben Nsir, Mahbouba Jguirim, Asma Belguith Sriha, Zohra Ben Salah Frih, Mohamed Hedi Bedoui
Publikováno v:
BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-12 (2024)
Abstract Background Cervical radiculopathy (CR) is a common condition, often associated with cervicogenic headache (CGH), a secondary headache arising from cervical spine disorders. Mechanical intermittent cervical traction (MICT) is frequently presc
Externí odkaz:
https://doaj.org/article/fb79dae0d3d044c8a9ca3259e3ba231e
Autor:
Ghada Ben Salah
Publikováno v:
Iranian Journal of Materials Science and Engineering, Vol 21, Iss 3, Pp 1-10 (2024)
This study reported the biological changes occurring after γ-irradiation of in vivo rat model and the osteochondral protective effect of Gelatine-Chitosan-Ginger (GEL-CH-GING). The results showed that Electron Paramagnetic Resonance (EPR) Spectrosco
Externí odkaz:
https://doaj.org/article/77ad8ec9af6b440b9b4c0f648a495eb4
Publikováno v:
foresight, 2024, Vol. 26, Issue 3, pp. 453-469.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/FS-08-2023-0168
Autor:
Nesrine Ben Salah, Maha Lahouel, Lella Douh, Khaoula Trimeche, Amina Aounallah, Amira Atig, Colandane Belajouza, Mohamed Denguesli
Publikováno v:
JEADV Clinical Practice, Vol 3, Iss 4, Pp 1212-1214 (2024)
Abstract Henoch–Schönlein purpura (HSP) is an immunoglobulin A (IgA)‐mediated small‐vessel vasculitis mostly observed in children and rarely in adults. It can affect many organs, mainly the skin, kidneys, joints, and gastrointestinal tract. We
Externí odkaz:
https://doaj.org/article/414cdd3c9a7b4becbfbf4dbda1b3ce90
Autor:
Fatema Habbash, Afif Ben Salah, Mohamed Hany Shehata, Basheer Makarem, Sadok Chlif, Amer Almarabheh, Abdelhalim Deifalla, Jaleela S. Jawad
Publikováno v:
BMC Medical Education, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Background We implemented a contextualized innovative mentorship program in the Clinical Master in Family Medicine (CMFM) program established in April 2020 at Arabian Gulf University. In this paper, we describe the process of this program an
Externí odkaz:
https://doaj.org/article/22864acf6f544480bcf0309e6149947a
Autor:
Amen Allah Nasr, Sawsen Bouzidi, Khaouala Bderi, Zeineb Ben Hassine, Samy Laayouni, Naouel Ben Salah, Najiba Fekih-Mrissa, Bassem Louzir, Brahim Nsiri
Publikováno v:
Journal of Applied Hematology, Vol 15, Iss 2, Pp 152-155 (2024)
Elliptocytes are most abundant in hereditary elliptocytosis. Isolated deletion 20q [del(20q)] associated with elliptocytosis in a patient with myelodysplastic syndrome (MDS) is very rare, and only a few cases are reported in the literature. This repo
Externí odkaz:
https://doaj.org/article/60fcfbcfef42414a81e761c8fc8b530d
Autor:
Rachida Lamiri, Ghada Habachi, Seyfeddine Zayani, Radhouane Ben Salah, Abir Daya, Mabrouk Abdelaali, Mongi Mekki, Nahla Kechiche, Lassaad Sahnoun
Publikováno v:
Radiology Case Reports, Vol 19, Iss 6, Pp 2362-2366 (2024)
Osteomyelitis is a rare infectious disease in children, predominantly affecting long bones; however, its clinical presentation can be ambiguous if the location is atypical. Costal osteomyelitis is very rare in children and can mimic other pathologies
Externí odkaz:
https://doaj.org/article/b3a829f684eb426ca041c7c4b4519956
Autor:
Fatema Habbash, Zainab Khamis, Zahra Alasfoor, Aayat Mahdi, Masooma Alsharkhat, Noor Hasan, Alaa Al Qari, Sadok Chlif, Amer Almarabheh, Afif Ben Salah
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
PurposeThis study aimed to explore attitudes, practices, and perceived barriers of primary care physicians (PCPs) toward depression screening in older people.MethodsThis cross-sectional study enrolled PCPs from randomly selected representative primar
Externí odkaz:
https://doaj.org/article/9601a122bfb34b4e9c28bd10d26addf6
Autor:
Ben Salah, Olfa, Jarboui, Anis
Publikováno v:
Journal of Economics, Finance and Administrative Science, 2024, Vol. 29, Issue 57, pp. 166-185.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/JEFAS-09-2021-0198
Autor:
Dhoha Ben Salah, Mouna Elleuch, Oumeyma Trimeche, Asma Zargni, Fakhri Kallabi, Salma Sakka, Fatma Mnif, Nabila Rekik, Nadia Charfi, Hassen Kamoun, Mouna Mnif Feki, Faten Hadj Kacem, Mohamed Abid
Publikováno v:
Annals of Child Neurology, Vol 32, Iss 2, Pp 130-134 (2024)
Purpose Allgrove syndrome, also known as “triple A” syndrome, is characterized by adrenal insufficiency, achalasia, and alacrimia. When neurological signs are also present, the condition is referred to as “4 A” syndrome. Methods We conducted
Externí odkaz:
https://doaj.org/article/047022b12fb7477588ee364b1bf1b2b8