Two Randomized Phase 3 Studies of Aducanumab in Early Alzheimer’s Disease von Budd Haeberlein, Samantha, Aisen, P.S., Barkhof, F., Chalkias, S., Chen, T., Cohen, S., Dent, G., Hansson, O., Harrison, K., von Hehn, C., Iwatsubo, T., Mallinckrodt, C., Mummery, C.J., Muralidharan, K.K., Nestorov, I., Nisenbaum, L., Rajagovindan, R., Skordos, L., Tian, Y., van Dyck, C.H., Vellas, B., Wu, S., Zhu, Y., Sandrock, A.

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Neutrino quasielastic scattering on nuclear targets: Parametrizing transverse enhancement (meson exchange currents) von Bodek, A., Budd, H. S., Christy, M. E.

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Promising Targets for the Treatment of Neurodegenerative Diseases von Budd Haeberlein, SL, Harris, TJR

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Sonographer interaction with artificial intelligence: collaboration or conflict? von Day, T. G., Matthew, J., Budd, S., Hajnal, J. V., Simpson, J. M., Razavi, R., Kainz, B.

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Interaction between clinicians and artificial intelligence to detect fetal atrioventricular septal defects on ultrasound: how can we optimize collaborative performance? von Day, T. G., Matthew, J., Budd, S. F., Venturini, L., Wright, R., Farruggia, A., Vigneswaran, T. V., Zidere, V., Hajnal, J. V., Razavi, R., Simpson, J. M., Kainz, B.

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EP01.08: Artificial intelligence to assist in the screening fetal anomaly ultrasound scan (PROMETHEUS): a randomised controlled trial von Day, T.G., Matthew, J., Budd, S., Venturini, L., Wright, R., Farruggia, A., Jamshidi, B., Syngelaki, A., Ling, H., Tan, M., Lai, J., Brown, M., To, M., Guy, G.P., Arechvo, A., Casagrandi, D., Akolekar, R., Nanda, S., Nicolaides, K., Kainz, B., Simpson, J., Hajnal, J., Razavi, R.

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Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function von Findlay, Amy S, Carter, Roderick N, Starbuck, Becky, McKie, Lisa, Nováková, Klára, Budd, Peter S, Keighren, Margaret A, Marsh, Joseph A, Cross, Sally H, Simon, Michelle M, Potter, Paul K, Morton, Nicholas M, Jackson, Ian J

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Outcomes when congenital heart disease is diagnosed antenatally versus postnatally in the UK: a retrospective population-based study von Peake, Lewis K, Draper, Elizabeth S, Budd, Judith L S, Field, David

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VP17.01: Exploring a new paradigm for the fetal anomaly ultrasound scan: artificial intelligence in real‐time von Matthew, J., Skelton, E., Day, T., Zimmer, V., Gomez, A., Wheeler, G., Toussaint, N., Liu, T., Budd, S., Lloyd, K., Wright, R., Deng, S., Ghavami, N., Sinclair, M., Meng, Q., Kainz, B., Schnabel, J., Rueckert, D., Razavi, R., Simpson, J., Hajnal, J.

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Investigating Partially Discordant Results in Phase 3 Studies of Aducanumab von Mallinckrodt, C., Tian, Y., Aisen, P. S., Barkhof, F., Cohen, S., Dent, G., Hansson, O., Harrison, K., Iwatsubo, T., Mummery, C. J., Muralidharan, K. K., Nestorov, I., Nisenbaum, L., Rajagovindan, R., von Hehn, C., van Dyck, C. H., Vellas, B., Wu, S., Zhu, Y., Sandrock, A., Chen, T., Budd Haeberlein, Samantha

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Mitochondria, Calcium Regulation, and Acute Glutamate Excitotoxicity in Cultured Cerebellar Granule Cells von Budd, Samantha L., Nicholls, David G.

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A Reevaluation of the Role of Mitochondria in Neuronal Ca2+ Homeostasis von Budd, S. L., Nicholls, D. G.

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Mitochondria and Neuronal Survival von Nicholls, David G, Budd, Samantha L

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White Matter Diffusion Properties in Chronic Temporomandibular Disorders: An Exploratory Analysis von Budd, Alexandra S., Huynh, Thi K. T., Seres, Peter, Beaulieu, Christian, Armijo-Olivo, Susan, Cummine, Jacqueline

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Neutrino quasielastic scattering on nuclear targets von Bodek, A, Budd, H S, Christy, M E

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Humanized MC1R transgenic mice reveal human specific receptor function von Jackson, Ian J., Budd, Peter S., Keighren, Margaret, McKie, Lisa

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Activation of the Receptor Tyrosine Kinase Kit Is Required for the Proliferation of Melanoblasts in the Mouse Embryo von Mackenzie, Marina A.F., Jordan, Siobhán A., Budd, Peter S., Jackson, Ian J.

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Functional variation of MC1R alleles from red-haired individuals von HEALY, Eugene, JORDAN, Siobhan A, BUDD, Peter S, SUFFOLK, Ruth, REES, Jonathan L, JACKSON, Ian J

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Assessing parenting capacity in a child welfare context von Budd, Karen S.

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Holt Oram syndrome: a registry-based study in Europe von Barisic, Ingeborg, Boban, Ljubica, Greenlees, Ruth, Garne, Ester, Wellesley, Diana, Calzolari, Elisa, Addor, Marie-Claude, Arriola, Larraitz, Bergman, Jorieke Eh, Braz, Paula, Budd, Judith Ls, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsoyr, Kari, McDonnell, Bob, Nelen, Vera, Pierini, Anna, Queisser-Wahrendorf, Annette, Rankin, Judith, Rissmann, Anke, Rounding, Catherine, Tucker, David, Verellen-Dumoulin, Christine, Dolk, Helen

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