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of 77
pro vyhledávání: '"Prince, Matthew"'
Autor:
Fukshansky, Lenny, Henshaw, Glenn, Liao, Philip, Prince, Matthew, Sun, Xun, Whitehead, Samuel
Publikováno v:
International Journal of Number Theory, vol. 9 no. 1 (2013) pg. 139--154
We study well-rounded lattices which come from ideals in quadratic number fields, generalizing some recent results of the first author with K. Petersen. In particular, we give a characterization of ideal well-rounded lattices in the plane and show th
Externí odkaz:
http://arxiv.org/abs/1207.2671
Autor:
Fukshansky, Lenny, Henshaw, Glenn, Liao, Philip, Prince, Matthew, Sun, Xun, Whitehead, Samuel
Publikováno v:
Discrete and Computational Geometry, vol. 48 no. 3 (2012), pg. 735--748
We investigate distribution of integral well-rounded lattices in the plane, parameterizing the set of their similarity classes by solutions of the family of Pell-type Diophantine equations of the form $x^2+Dy^2=z^2$ where $D>0$ is squarefree. We appl
Externí odkaz:
http://arxiv.org/abs/1205.5301
Akademický článek
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Autor:
King, Alexander H., Krych, Aaron J., Prince, Matthew R., Pareek, Ayoosh, Stuart, Michael J., Levy, Bruce A.
Publikováno v:
In Arthroscopy: The Journal of Arthroscopic and Related Surgery September 2016 32(9):1814-1819
Autor:
King, Alexander H., Prince, Matthew R., Reardon, Patrick J., Levy, Bruce A., Stuart, Michael J.
Publikováno v:
In Operative Techniques in Sports Medicine December 2015 23(4):302-306
Autor:
Prince, Matthew R., King, Alexander H., Shin, Alexander Y., Bishop, Allen T., Stuart, Michael J., Levy, Bruce A.
Publikováno v:
In Operative Techniques in Sports Medicine December 2015 23(4):357-361
Autor:
Kwabena Onwona-Agyeman, Stella Elikplim Lawerteh, Sheila Asamoah-Okyere, Sandra Laryea Odai, Sandra Kwarteng Owusu, Gabrielle Obeng-Koranteng, Kevin Bonsu, Prince Matthew Oduah-Odoom, Marco Zampoli, Naomi Dianna Adjetey, Marie Charlyne Fatima Kilba, Parbie Abbeyquaye, Selorm Afidemenyo
Publikováno v:
Journal of the Pan African Thoracic Society; Vol. 2 No. 3 (2021); 167-170
Cystic fibrosis (CF) is a severe life-limiting genetic disorder resulting from mutations in the cystic fibrosis transmembrane regulator gene and is reported to be more prevalent among Caucasians than people of African descent. The past three decades
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adb653cf2c47d38778dc6a86e80abffc
https://doi.org/10.25259/jpats_10_2021
https://doi.org/10.25259/jpats_10_2021
Autor:
Sandbrink, Friedhelm, Murphy, Jennifer L., Johansson, Melanie, Olson, Juli L., Edens, Ellen, Clinton-Lont, Jamie, Sall, James, Spevak, Christopher, MD, Ellen Edens, Brown, Nicole, Guinta, Raquel, Macedo, Franz, Nazario, Mitchell, Pangarkar, Sanjog, Preston, Samuel, Prince, Matthew, Real, Donna Endsley, Riegleman, David, Steil, Evan, Institute, ECRI
Publikováno v:
Annals of Internal Medicine; Mar2023, Vol. 176 Issue 3, p388-397, 10p, 1 Chart, 1 Graph
Akademický článek
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Publikováno v:
In Pathology February 2023 55 Supplement 1:S92-S92