Zobrazeno 1 - 10
of 404
pro vyhledávání: '"A. Mhanni"'
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100666- (2020)
Glutaric aciduria type 1 (GA1) is a severe inherited neurometabolic disorder whose clinical outcome has improved after implementation of newborn screening (NBS) programs and prompt beginning of guideline-directed presymptomatic metabolic treatment. W
Externí odkaz:
https://doaj.org/article/2d107906185540688280fc8c385aa0ea
Autor:
Alison H. Howie, Kylie Tingley, Michal Inbar-Feigenberg, John J. Mitchell, Kim Angel, Jenifer Gentle, Maureen Smith, Martin Offringa, Nancy J. Butcher, Philippe M. Campeau, Pranesh Chakraborty, Alicia Chan, Dean Fergusson, Eva Mamak, Peyton McClelland, Saadet Mercimek-Andrews, Aizeddin Mhanni, Zeinab Moazin, Cheryl Rockman-Greenberg, C. Anthony Rupar, Becky Skidmore, Sylvia Stockler, Kednapa Thavorn, Alexandra Wyatt, Beth K. Potter, INFORM RARE Network
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-15 (2024)
Abstract Background To inform the development of a core outcome set (COS) for children and youth with mucopolysaccharidoses (MPS), we aimed to identify all outcomes and associated outcome measurement instruments that are reported in recent clinical t
Externí odkaz:
https://doaj.org/article/3f5faa2b5e894b579d9b0f0a9ed05831
Publikováno v:
Journal of Medical Education Development, Vol 17, Iss 53, Pp 63-71 (2024)
Background & Objective: In dental education, understanding optimal assessment methods and factors like stress and confidence is essential. This research assessed second-year dental students' performance in fixed prosthodontics using multiple-choice q
Externí odkaz:
https://doaj.org/article/9ae5d4a37e0d4d6fb4b439f8e74338e9
Autor:
Ryan Iverson, Monica Taljaard, Michael T. Geraghty, Michael Pugliese, Kylie Tingley, Doug Coyle, Jonathan B. Kronick, Kumanan Wilson, Valerie Austin, Catherine Brunel-Guitton, Daniela Buhas, Nancy J. Butcher, Alicia K. J. Chan, Sarah Dyack, Sharan Goobie, Cheryl R. Greenberg, Shailly Jain-Ghai, Michal Inbar-Feigenberg, Natalya Karp, Mariya Kozenko, Erica Langley, Matthew Lines, Julian Little, Jennifer MacKenzie, Bruno Maranda, Saadet Mercimek-Andrews, Aizeddin Mhanni, John J. Mitchell, Laura Nagy, Martin Offringa, Amy Pender, Murray Potter, Chitra Prasad, Suzanne Ratko, Ramona Salvarinova, Andreas Schulze, Komudi Siriwardena, Neal Sondheimer, Rebecca Sparkes, Sylvia Stockler-Ipsiroglu, Kendra Tapscott, Yannis Trakadis, Lesley Turner, Clara Van Karnebeek, Anthony Vandersteen, Jagdeep S. Walia, Brenda J. Wilson, Andrea C. Yu, Beth K. Potter, Pranesh Chakraborty
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Background Generating rigorous evidence to inform care for rare diseases requires reliable, sustainable, and longitudinal measurement of priority outcomes. Having developed a core outcome set for pediatric medium-chain acyl-CoA dehydrogenase
Externí odkaz:
https://doaj.org/article/7eb12ffd1f3f4a9898861100013c4093
Publikováno v:
Journal of Dental Research, Dental Clinics, Dental Prospects, Vol 17, Iss 3, Pp 162-169 (2023)
Background. Dental students learn and practice clinical procedures in clinical skills laboratories. These practices are graded by qualified staff to evaluate the effectiveness of their learning. Valid evaluation requires accuracy and reliability. Alt
Externí odkaz:
https://doaj.org/article/db6a4d4236ff48bf836111ae50deddeb
Publikováno v:
Journal of Medical Education Development. 2024, Vol. 17 Issue 53, p63-71. 9p.
Akademický článek
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Autor:
Mhanni Youssef, Lagmich Youssef
Publikováno v:
EPJ Photovoltaics, Vol 15, p 31 (2024)
In recent years, there has been a growing interest in photovoltaic (PV) systems due to their capacity to generate clean energy, reduce pollution, and promote environmental sustainability. Optimizing the operational efficiency of PV systems has become
Externí odkaz:
https://doaj.org/article/f9ee7905a5cf4732b1fcd185cfdb1303
Publikováno v:
Bone Reports, Vol 17, Iss , Pp 101617- (2022)
Asfotase alfa is a human recombinant enzyme replacement therapy for hypophosphatasia. We describe 6 adults who were treated with asfotase alfa for 61–68 months in a clinical trial (NCT01163149), after which asfotase alfa was discontinued for 15–4
Externí odkaz:
https://doaj.org/article/cf3c163cd37b4b7d946b76ef17a0a982
Akademický článek
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