Management of Hyperbilirubinemia in Newborn Infants

Displaying 1 - 5 of 5CSV
Manzoni, E., Carli, S., Gaignard, P., Schlieben, L. D., Hirano, M., Ronchi, D., Gonzales, E., Shimura, M., Murayama, K., Okazaki, Y., Barić, I., Petkovic Ramadza, D., Karall, D., Mayr, J., Martinelli, D., La Morgia, C., Primiano, G., Santer, R., Servidei, S., … Garone, C. (2024). Deoxyguanosine kinase deficiency: natural history and liver transplant outcome. Brain Communications, 6(3). https://doi.org/10.1093/braincomms/fcae160
Publication Date
Carter, R. C. (2024). The critical need for novel precision medicine methodologies in fetal alcohol spectrum disorders. The American Journal of Clinical Nutrition, 119(1), 5–6. https://doi.org/10.1016/j.ajcnut.2023.10.027
Publication Date
Mohan, S., Geck, R., Fayer, S., Donnelly, R., Relling, M., Vulliamy, T., Caudle, K., Waddell, A., Kendall, E., Domingo, G., Minucci, A., Ley, B., Chu, C., Haidar, C., McLeod, H., Prchal, J., Sirdah, M., Aggarwal, V., Jiang, W., … Stergachis, A. (2024). P008: ClinGen Glucose-6-phosphate dehydrogenase (G6PD) Variant Curation Expert Panel: Addressing the need for genetic variant classification in G6PD deficiency*. Genetics in Medicine Open, 2, 100885. https://doi.org/10.1016/j.gimo.2024.100885
Publication Date
Moore, A., Busch, M. P., Dziewulska, K., Francis, R. O., Hod, E. A., Zimring, J. C., D’Alessandro, A., & Page, G. P. (2022). Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. Journal of Biological Chemistry, 298(12), 102706. https://doi.org/10.1016/j.jbc.2022.102706
Publication Date
Ganapathi, M., Campbell, P., Ofori, K., Aggarwal, V., Francis, R. O., & Kratz, A. (2022). Impact of pre‐emptive rapid testing for glucose‐6‐phosphate dehydrogenase deficiency prior to rasburicase administration at a tertiary care centre: A retrospective study. British Journal of Clinical Pharmacology, 88(9), 4163–4170. Portico. https://doi.org/10.1111/bcp.15353
Publication Date