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pro vyhledávání: '"Olaye, A"'
Autor:
Olayé, Jules, Tomasevic, Milica
In this article, we investigate the ergodic behaviour of a multidimensional age-dependent branching process with a singular jump kernel, motivated by studying the phenomenon of telomere shortening in cell populations. Our model tracks individuals evo
Externí odkaz:
http://arxiv.org/abs/2408.02476
Autor:
Olayé, Jules, Bouzidi, Hala, Aristov, Andrey, Ramos, Salomé Gutiérrez, Baroud, Charles, Bansaye, Vincent
The growth of a population is often modeled as branching process where each individual at the end of its life is replaced by a certain number of offspring. An example of these branching models is the Bellman-Harris process, where the lifetime of indi
Externí odkaz:
http://arxiv.org/abs/2402.03842
We show we can control an epidemic reaction-diffusion on a directed, and heterogeneous, network by redirecting the flows, thanks to the optimisation of well-designed loss functions, in particular the basic reproduction number of the model. We provide
Externí odkaz:
http://arxiv.org/abs/2202.02017
Autor:
Brown, Sherry-Ann, Beavers, Craig, Bauer, Brenton, Cheng, Richard K., Berman, Generika, Marshall, Catherine H., Guha, Avirup, Jain, Prantesh, Steward, Austin, DeCara, Jeanne M., Olaye, Iredia M., Hansen, Kathryn, Logan, Jim, Bergom, Carmen, Glide-Hurst, Carri, Loh, Irving, Gambril, John Alan, MacLeod, James, Maddula, Ragasnehith, McGranaghan, Peter J., Batra, Akshee, Campbell, Courtney, Hamid, Abdulaziz, Gunturkun, Fatma, Davis, Robert, Jefferies, John, Fradley, Michael, Albert, Katherine, Blaes, Anne, Choudhuri, Indrajit, Ghosh, Arjun K., Ryan, Thomas D., Ezeoke, Ogochukwu, Leedy, Douglas J., Williams, Wadsworth, Roman, Sebastian, Lehmann, Lorenz, Sarkar, Abdullah, Sadler, Diego, Polter, Elizabeth, Ruddy, Kathryn J., Bansal, Neha, Yang, Eric, Patel, Brijesh, Cho, David, Bailey, Alison, Addison, Daniel, Rao, Vijay, Levenson, Joshua E., Itchhaporia, Dipti, Watson, Karol, Gulati, Martha, Williams, Kim, Lloyd-Jones, Donald, Michos, Erin, Gralow, Julie, Martinez, Hugo
Publikováno v:
In American Heart Journal Plus: Cardiology Research and Practice February 2024 38
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-17 (2023)
Abstract Objective To understand the benefit-risk profile for historical and current treatments for MLD. Methods A systematic review was conducted on the effectiveness, safety, and costs of MLD treatments: allogeneic haematopoietic stem cell transpla
Externí odkaz:
https://doaj.org/article/35522a495033463991e77a95135e1294
Autor:
Sherry-Ann Brown, Craig Beavers, Brenton Bauer, Richard K. Cheng, Generika Berman, Catherine H. Marshall, Avirup Guha, Prantesh Jain, Austin Steward, Jeanne M. DeCara, Iredia M. Olaye, Kathryn Hansen, Jim Logan, Carmen Bergom, Carri Glide-Hurst, Irving Loh, John Alan Gambril, James MacLeod, Ragasnehith Maddula, Peter J. McGranaghan, Akshee Batra, Courtney Campbell, Abdulaziz Hamid, Fatma Gunturkun, Robert Davis, John Jefferies, Michael Fradley, Katherine Albert, Anne Blaes, Indrajit Choudhuri, Arjun K. Ghosh, Thomas D. Ryan, Ogochukwu Ezeoke, Douglas J. Leedy, Wadsworth Williams, Sebastian Roman, Lorenz Lehmann, Abdullah Sarkar, Diego Sadler, Elizabeth Polter, Kathryn J. Ruddy, Neha Bansal, Eric Yang, Brijesh Patel, David Cho, Alison Bailey, Daniel Addison, Vijay Rao, Joshua E. Levenson, Dipti Itchhaporia, Karol Watson, Martha Gulati, Kim Williams, Donald Lloyd-Jones, Erin Michos, Julie Gralow, Hugo Martinez
Publikováno v:
American Heart Journal Plus, Vol 38, Iss , Pp 100354- (2024)
As cancer therapies increase in effectiveness and patients' life expectancies improve, balancing oncologic efficacy while reducing acute and long-term cardiovascular toxicities has become of paramount importance. To address this pressing need, the Ca
Externí odkaz:
https://doaj.org/article/8043007b5ee04ac89d1b9f4d2fd3cdc7
Autor:
Nicola Specchio, Paul Gissen, Emily de Los Reyes, Andrew Olaye, Charlotte Camp, Tristan Curteis, Annabel Griffiths, Thomas Butt, Jessica Cohen-Pfeffer, Peter Slasor, Zlatko Sisic, Mohit Jain, Angela Schulz
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0302382 (2024)
BackgroundThe CLN2 Clinical Rating Scale evaluates disease progression in CLN2 disease, an ultra-rare, neurodegenerative disorder with late infantile onset. To validate the Clinical Rating Scale, a comparison with the Pediatric Quality of Life Invent
Externí odkaz:
https://doaj.org/article/ffa584edb7444e39bb9066a50015e6e3
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