Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Vivian Cruz"'
Publikováno v:
Journal of Economics Finance and Administrative Science, Vol 29, Iss 57, Pp 57-76 (2024)
Purpose – The purpose of this paper is to determine the impact of private and public initiatives (financial literacy, entrepreneurship, remote work and government aid) on individual job loss and decrease in income during the COVID-19 pandemic in Pe
Externí odkaz:
https://doaj.org/article/823a47b3403347df854a1de9478c13ef
Autor:
Maria Al Bandari, Laura Nagy, Vivian Cruz, Stacy Hewson, Alomgir Hossain, Michal Inbar-Feigenberg
Publikováno v:
International Journal of Neonatal Screening, Vol 10, Iss 2, p 29 (2024)
Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a rare genetic condition affecting the mitochondrial beta-oxidation of long-chain fatty acids. This study reports on the clinical outcomes of patients diagnosed by newborn screening with VL
Externí odkaz:
https://doaj.org/article/1a262141ea4b4bc3a477e5045742b25c
Publikováno v:
Journal of Economics Finance and Administrative Science, Vol 27, Iss 54, Pp 376-393 (2022)
Purpose – Our findings indicate that workers with more financial education were more prepared to face the negative effects on their finances from COVID. This ability reduces the probability of becoming financially fragile and experiencing financial
Externí odkaz:
https://doaj.org/article/dbe30568ffa141a880dce7f39e5c46b4
Publikováno v:
JIMD Reports, Vol 55, Iss 1, Pp 22-25 (2020)
Abstract Combined methylmalonic aciduria and homocystinuria (cobalamin C deficiency, cblC) is a well‐described disorder of vitamin B12 metabolism caused by mutations in the MMACHC gene with multisystemic manifestations. While there is no cure, comb
Externí odkaz:
https://doaj.org/article/73873a681f934dc7a4aaaf054e7188f6
Autor:
Ryan D. Wuebbles, Vivian Cruz, Pam Van Ry, Pamela Barraza-Flores, Paul D. Brewer, Peter Jones, Dean J. Burkin
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 13, Iss , Pp 145-153 (2019)
Duchenne muscular dystrophy (DMD) is a devastating disease caused by mutations in the dystrophin gene that result in the complete absence of dystrophin protein. We have shown previously that recombinant mouse Galectin-1 treatment improves physiologic
Externí odkaz:
https://doaj.org/article/7cb9207feebe46a59941dbb479c9bbe1
Publikováno v:
Memorias del Concurso Lasallista de Investigación, Desarrollo e innovación. 8:38-41
Pachuca con parámetros precisos para determinar las condiciones de ventilación y confort para un regreso seguro a clases presenciales. Mediante equipos especializados se realizaron mediciones de temperatura, humedad relativa y CO2 en el interior de
Autor:
Pam Van Ry, Ryan D. Wuebbles, Pamela Barraza-Flores, Peter L. Jones, Vivian Cruz, Dean J. Burkin, Paul Duffield Brewer
Publikováno v:
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 13, Iss, Pp 145-153 (2019)
Molecular Therapy: Methods & Clinical Development, Vol 13, Iss, Pp 145-153 (2019)
Duchenne muscular dystrophy (DMD) is a devastating disease caused by mutations in the dystrophin gene that result in the complete absence of dystrophin protein. We have shown previously that recombinant mouse Galectin-1 treatment improves physiologic
Autor:
Samuel Mongrut, Vivian Cruz
Publikováno v:
FUZZY ECONOMIC REVIEW. 26
Autor:
Andreas Schulze, Komudi Siriwardena, Lizbeth E. Mellin‐Sanchez, Julian Raiman, Vivian Cruz, Saadet Mercimek-Andrews, Danielle K. Bourque, Anette Feigenbaum, Stacy Hewson, Garrett Bullivant
Publikováno v:
JIMD Reports
Biallelic variants in MMACHC results in the combined methylmalonic aciduria and homocystinuria, called cobalamin (cbl) C (cblC) deficiency. We report 26 patients with cblC deficiency with their phenotypes, genotypes, biochemical parameters, and treat
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.