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BMC Cancer|April 26, 2023
Impact of pharmacogenomic DPYD variant guided dosing on toxicity in patients receiving fluoropyrimidines for gastrointestinal cancers in a high-volume tertiary centreDavid K Lau, Caroline Fong, Faten Arouri, et al.
Mbio|July 4, 2019
Zika Virus-Immune Plasmas from Symptomatic and Asymptomatic Individuals Enhance Zika Pathogenesis in Adult and Pregnant MiceByoung-Shik Shim, Young-Chan Kwon, Michael J Ricciardi, et al.
Implementation Science Communications|March 21, 2024
Scaling-up and scaling-out the Systems Analysis and Improvement Approach to optimize the hypertension diagnosis and care cascade for HIV infected individuals (SCALE SAIA-HTN): a stepped-wedge cluster randomized trialCarmen E Hazim, Igor Dobe, Stephen Pope, et al.
Current Oncology (Toronto, Ont.)|April 21, 2022
Ibrutinib in c-MYC and HER2 Amplified Oesophagogastric Carcinoma: Results of the Proof-of-Concept iMYC StudyFiona Turkes, Annette Bryant, Ruwaida Begum, et al.
Implementation Science : IS|November 17, 2022
Economic evaluation of implementation science outcomes in low- and middle-income countries: a scoping reviewAkash Malhotra, Ryan R Thompson, Faith Kagoya, et al.
European Journal of Cancer (Oxford, England : 1990)|July 14, 2020
Defining the true impact of coronavirus disease 2019 in the at-risk population of patients with cancerVasileios Angelis, Zayd Tippu, Kroopa Joshi, et al.
Orphanet Journal of Rare Diseases|September 20, 2014
Single point mutation in Rabenosyn-5 in a female with intractable seizures and evidence of defective endocytotic traffickingSylvia Stockler, Silvia Corvera, David Lambright, et al.
American Journal of Human Genetics|June 18, 2002
Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173LDavid Watkins, Ming Ru, Hye-Yeon Hwang, et al.
BMJ Global Health|October 8, 2020
Protecting essential health services in low-income and middle-income countries and humanitarian settings while responding to the COVID-19 pandemicKarl Blanchet, Ala Alwan, Caroline Antoine, et al.
JAMA Neurology|May 7, 2014
Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegiaAlexander Lossos, Omri Teltsh, Tsipi Milman, et al.
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