Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Jacob, Arthur"'
Autor:
Agarwal, Arav, Mittal, Karthik, Doyle, Aidan, Sridhar, Pragnya, Wan, Zipiao, Doughty, Jacob Arthur, Savelka, Jaromir, Sakr, Majd
We conduct a preliminary study of the effect of GPT's temperature parameter on the diversity of GPT4-generated questions. We find that using higher temperature values leads to significantly higher diversity, with different temperatures exposing diffe
Externí odkaz:
http://arxiv.org/abs/2404.09366
Publikováno v:
Osteology, Vol 3, Iss 4, Pp 122-130 (2023)
Background: Displaced talar neck fractures are subject to avascular necrosis and degenerative joint disease. A single-lateral-incision approach may avoid damage to the remaining blood supply to the talar body provided by the deltoid artery. The purpo
Externí odkaz:
https://doaj.org/article/4b56c57cda484c00b9dd4d9ddae51c39
Autor:
Mitchell C. Harris, Gregory Lause, Alicia Unangst, Jacob Arthur, Daniel Song, Michael Lustik, Kenneth K. Lindell, Paul Ryan
Publikováno v:
Foot & Ankle International. 43:923-927
Background: Malreduction after syndesmotic stabilization occurs in as many as 52% of cases and has been shown to detrimentally affect clinical outcomes. We propose that the modified Glide Path technique reduces the occurrence of syndesmotic malreduct
Autor:
Nair, Divya, Li, Dong, Erdogan, Hannah, Yoon, Andrew, Harr, Margaret H., Bergant, Gaber, Peterlin, Borut, Pušenjak, Maruša Škrjanec, Jayakar, Parul, Pfundt, Rolph, Jansen, Sandra, McWalter, Kirsty, Sidhu, Alpa, Saliganan, Sheila, Agolini, Emanuele, Jacob, Arthur, Pasquier, Jennifer, Arash, Rafii, Kahrizi, Kimia, Najmabadi, Hossein, Ropers, Hans-Hilger, Bhoj, Elizabeth J.
Publikováno v:
Human Genetics and Genomics Advances, 3(4):100122. Cell Press
Nair, D, Li, D, Erdogan, H, Yoon, A, Harr, M H, Bergant, G, Peterlin, B, Pušenjak, M Š, Jayakar, P, Pfundt, R, Jansen, S, McWalter, K, Sidhu, A, Saliganan, S, Agolini, E, Jacob, A, Pasquier, J, Arash, R, Kahrizi, K, Najmabadi, H, Ropers, H-H & Bhoj, E J 2022, ' Erratum : Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3 (Human Genetics and Genomics Advances (2021) 2(2), (S2666247721000051), (10.1016/j.xhgg.2021.100024)) ', Human Genetics and Genomics Advances, vol. 3, no. 4, 100122 . https://doi.org/10.1016/j.xhgg.2022.100122
Nair, D, Li, D, Erdogan, H, Yoon, A, Harr, M H, Bergant, G, Peterlin, B, Pušenjak, M Š, Jayakar, P, Pfundt, R, Jansen, S, McWalter, K, Sidhu, A, Saliganan, S, Agolini, E, Jacob, A, Pasquier, J, Arash, R, Kahrizi, K, Najmabadi, H, Ropers, H-H & Bhoj, E J 2022, ' Erratum : Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3 (Human Genetics and Genomics Advances (2021) 2(2), (S2666247721000051), (10.1016/j.xhgg.2021.100024)) ', Human Genetics and Genomics Advances, vol. 3, no. 4, 100122 . https://doi.org/10.1016/j.xhgg.2022.100122
(Human Genetics and Genomics Advances 2, 100024; April 8, 2021) Patients 3-1 and 3-2 (siblings) were tested at GeneDx. They were compound heterozygous for p.Arg1472Glu and c.3434del p.Lys1145fs∗7. However c.3434del p.Lys1145fs∗7 was noted as p.Le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1c9b1d9e64915d2b2faf7bde0da5457b
https://research.vumc.nl/en/publications/d1081a11-50ae-4e00-89a7-db8f8dfe0bee
https://research.vumc.nl/en/publications/d1081a11-50ae-4e00-89a7-db8f8dfe0bee
Autor:
Jacob, Arthur.
Publikováno v:
Search Pathfinder by call number to request from NRLF..
Thesis (doctoral)--Universität Breslau.
Externí odkaz:
http://sunsite2.berkeley.edu:8000/"target="_blank
Autor:
Jacob, Arthur
Publikováno v:
Philosophical Transactions of the Royal Society of London, 1819 Jan 01. 109, 300-307.
Externí odkaz:
https://www.jstor.org/stable/107507