Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shaun Charkowick"'
Autor:
Aryanna Jordan, Constantine Logothetis, Catherine H. Hanna, Shaun Charkowick, Sherry Zhang, Asa Oxner, Thomas A. Weppelmann
Publikováno v:
JAMA Network Open
This prognostic study evaluates the use of plasma D-dimer concentrations to rule out pulmonary embolism among patients hospitalized with COVID-19.
Autor:
Sherri Huang, Ashley Perry, Carlos Sanchez Parra, Adriana Gonzalez Torriente, Haider Ghumman, Shaun Charkowick, Joshua Colon, Mckenzi Heide, Michael Jaglal, Rahul Mhaskar, Juan Felipe Rico
Publikováno v:
Blood. 140:2782-2782
Autor:
Jin Li, Peng Yu, Nurit Ballas, Mary F. Kritzer, Ariel Karten, Shaun Charkowick, Jialin Sun, Sivan Osenberg, Christy A. Felice, Minh Vu Chuong Nguyen
Publikováno v:
Proceedings of the National Academy of Sciences. 115
Rett syndrome (RTT) is a severe neurodevelopmental disorder that affects about 1 in 10,000 female live births. The underlying cause of RTT is mutations in the X-linked gene, methyl-CpG-binding protein 2 (MECP2); however, the molecular mechanism by wh
Autor:
Huang, Sherri1 (AUTHOR) huang22@usf.edu, Perry, Ashley1 (AUTHOR), Sanchez Parra, Carlos1,2 (AUTHOR), Gonzalez Torriente, Adriana3 (AUTHOR), Ghumman, Haider3 (AUTHOR), Charkowick, Shaun3 (AUTHOR), Colon, Joshua3 (AUTHOR), Heide, McKenzi3 (AUTHOR), Jaglal, Michael4,5 (AUTHOR), Mhaskar, Rahul3 (AUTHOR), Rico, Juan Felipe6 (AUTHOR)
Publikováno v:
Journal of Clinical Medicine. May2024, Vol. 13 Issue 10, p2974. 9p.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 6/5/2018, Vol. 115 Issue 23, p5835-5838, 4p
Autor:
Fang Du, Nguyen, Minh Vu Chuong, Karten, Ariel, Felice, Christy A., Mandel, Gail, Ballas, Nurit
Publikováno v:
Human Molecular Genetics; 5/1/2016, Vol. 25 Issue 9, p1690-1702, 13p
Autor:
Logothetis, Constantine N., Weppelmann, Thomas A., Jordan, Aryanna, Hanna, Catherine, Zhang, Sherry, Charkowick, Shaun, Oxner, Asa
Publikováno v:
JAMA Network Open; 10/8/2021, Vol. 4 Issue 10, pe2128802-e2128802, 1p