Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Nadia Al-Wardy"'
Autor:
Ken Masters, Nadia Al-Wardy
Publikováno v:
F1000Research, Vol 10 (2021)
Determining a Hofstee cut-off point in medical education student assessment is problematic: traditional methods can be time-consuming, inaccurate, and inflexible. To counter this, we developed a simple Android app that receives raw, unsorted student
Externí odkaz:
https://doaj.org/article/3f3ffc8a79e84c6a9efeae65195555ad
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 20, Iss 2, Pp e187-e187 (2020)
Objectives: After completing the pre-clinical phase of a Doctor of Medicine (MD) curriculum, undergraduate medical students may choose to add a Bachelor of Science (BSc) degree in health sciences to their MD degree. Limited data exists on the motives
Externí odkaz:
https://doaj.org/article/cbf88881eefb44ea99be5114c31282d8
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 3, Iss 1, Pp 9-12 (2001)
Objective: To develop a polymerase chain reaction (PCR) based test for the detection of a common frame-shift mutation (35delG) in the connexin-26 (GJB2) gene, and to investigate the status of this mutation in Oman. Method: A PCR test, based on sitedi
Externí odkaz:
https://doaj.org/article/3b8bc7d74f474fc9abb59fe95d034047
Publikováno v:
Sultan Qaboos University Medical Journal [SQUMJ]. 21:e191-194
COVID-19 has gripped the world with lightning speed. Since the onset of the pandemic, activity throughout the world came to a grinding halt. However, business had to continue and people have to learn to live with the virus while the pandemic continue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcf652e314f2af15764204436fc62e56
https://doi.org/10.18295/squmj.2021.21.02.006
https://doi.org/10.18295/squmj.2021.21.02.006
Autor:
Khalsa Ahmad Al-Lamki, Tommaso Pippucci, Mazin Jawad Al-Khabouri, Mohammed Al-Kindi, Flavia Palombo, Nadia Al-Wardy, Giovanni Romeo
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 18, Iss 1, Pp 1-12 (2020)
Journal of Genetic Engineering & Biotechnology
Journal of Genetic Engineering & Biotechnology
BackgroundHereditary hearing loss is a heterogeneous group of complex disorders with an overall incidence of one in every 500 newborns presented as syndromic and non-syndromic forms. Cadherin-related 23 (CDH23) is one of the listed deafness causative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d13c8b87c3c7faa3f2d86cb269c60cb9
https://doi.org/10.1186/s43141-020-0021-4
https://doi.org/10.1186/s43141-020-0021-4
Autor:
Giulia Severi, Francesco Pisani, Duccio Maria Cordelli, Nayereh Nouri, Mohammed Nasser Al Kindi, Alfredo Brusco, Flavia Palombo, Caterina Marconi, Pamela Magini, Tommaso Pippucci, Claudio Graziano, Nadia Al Wardy, Gaetano Cantalupo, Mansoor Salehi, Giovanni Romeo, Elisa Giorgio, Mazin Al Khabouri, Simone Gangarossa, Marco Seri, Valerio Carelli, Chiara La Morgia
Autozygosity-driven exome analysis has been shown effective for identification of genes underlying recessive diseases especially in countries of the so-called Greater Middle East (GME), where high consanguinity unravels the phenotypic effects of rece
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d93c669a8cc90cf54ea41bbc683c0e7
https://hdl.handle.net/11573/1669610
https://hdl.handle.net/11573/1669610
Publikováno v:
Saudi Medical Journal, Vol 37, Iss 10, Pp 1068-1075 (2016)
Saudi Medical Journal
Saudi medical journal
Saudi Medical Journal
Saudi medical journal
Objectives: To identify genetic defects in an Omani family diagnosed with deafness. Methods: A cross-sectional association study was conducted at the Department of Biochemistry, College of Medicine and Health Sciences, Sultan Qaboos University, Al-Kh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0555dd01533d18b5c8cacef9964e481c
https://doi.org/10.15537/smj.2016.10.14967
https://doi.org/10.15537/smj.2016.10.14967
Autor:
Nadia Al Wardy
Publikováno v:
Sultan Qaboos University Medical Journal
Faculty development is necessary to improve and update teaching and learning methodologies. As such, a variety of learning activities have been designed to improve teaching competencies of individual teachers. The College of Medicine & Health Science
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06c29011829c3a8bd19539768602efc1
https://doi.org/10.18295/squmj.2020.20.03.005
https://doi.org/10.18295/squmj.2020.20.03.005
Autor:
Manir Ali, Khalsa Al Lamki, Mohammed E El-Asrag, Ahlam Gabr, Chris F. Inglehearn, Mazin Al Khabouri, Mohammed Al-Kindi, Ahmed H Al-Amri, Ahmed B. Idris, Nadia Al Wardy, Steven J. Clapcote, Abeer Al Saegh, Watfa Al-Mamari
Publikováno v:
European journal of medical genetics. 62(12)
Hearing loss is a debilitating disorder that impairs language acquisition, resulting in disability in children and potential isolation in adulthood. Its onset can have a genetic basis, though environmental factors, which are often preventable, can al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45f162b13f80e6eac18616be060135d4
https://pubmed.ncbi.nlm.nih.gov/30476627
https://pubmed.ncbi.nlm.nih.gov/30476627
Autor:
Guido Alberto Gnecchi Ruscone, Mohammed Nasser Al Kindi, Marco Seri, Tania Giangregorio, Andrea Angius, Tommaso Pippucci, Paolo Gasparini, Manuela Oppo, Giorgia Girotto, Marco Sazzini, Flavia Palombo, Nadia Al-Wardy, Mazin Al Khabori, Khalsa Al Lamki, Matteo Benelli, Francesco Cucca, Alberto Magi, Giovanni Romeo
Publikováno v:
Journal of human genetics. 62(2)
The increased risk for autosomal recessive disorders is one of the most well-known medical implications of consanguinity. In the Sultanate of Oman, a country characterized by one of the highest rates of consanguineous marriages worldwide, prevalence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c20b582487166c73b78058776bd9fbf9
https://pubmed.ncbi.nlm.nih.gov/27734841
https://pubmed.ncbi.nlm.nih.gov/27734841