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Plos Medicine|June 24, 2021
Achieving global mortality reduction targets and universal health coverage: The impact of COVID-19Wenhui Mao, Osondu Ogbuoji, David Watkins, et al.
Plos One|April 10, 2024
Health and economic burden of insufficient physical activity in Saudi ArabiaSaleh A Alqahtani, Reem AlAhmed, Mariam M Hamza, et al.
Human Mutation|April 17, 2009
Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlationsJordan P Lerner-Ellis, Natascia Anastasio, Junhui Liu, et al.
Journal of Inherited Metabolic Disease|October 9, 2021
Methionine synthase deficiency: Variable clinical presentation and benefit of early diagnosis and treatmentKimberly A Kripps, Leighann Sremba, Austin A Larson, et al.
Human Molecular Genetics|July 5, 2013
Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemiaMa'atem B Fofou-Caillierez, Nadir T Mrabet, Céline Chéry, et al.
Human Molecular Genetics|April 28, 2017
Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalitiesAnita M Quintana, Hung-Chun Yu, Alison Brebner, et al.
Implementation Science Communications|June 12, 2026
Evaluating implementation of the HEARTS model for management of hypertension and diabetes in Guatemala: protocol for a prospective observational hybrid type 3 studyDavid Flood, Irmgardt Alicia María Wellmann Castellanos, Luis Fernando Ayala, et al.
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