Zobrazeno 1 - 10
of 126
pro vyhledávání: '"Craige C"'
Autor:
Steiner, Robert A., Hohmann, John G., Holmes, Andrew, Wrenn, Craige C., Cadd, Gary, Juréus, Anders, Clifton, Donald K., Luo, Mulon, Gutshall, Mitchell, Ma, Shuang Y., Mufson, Elliott J., Crawley, Jacqueline N.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2001 Mar . 98(7), 4184-4189.
Externí odkaz:
https://www.jstor.org/stable/3055391
Autor:
Wrenn, Craige C.1 (AUTHOR) craige.wrenn@drake.edu, French, Eric2 (AUTHOR), Baker, Dustin3 (AUTHOR), McCallian, Randall3 (AUTHOR), Kirk, Ryan3 (AUTHOR), Reilly, Mark P.2 (AUTHOR), Valdovinos, Maria G.3 (AUTHOR)
Publikováno v:
Psychopharmacology. Apr2021, Vol. 238 Issue 4, p1133-1140. 8p. 1 Chart, 3 Graphs.
Autor:
Mark P. Reilly, Craige C. Wrenn, Maria G. Valdovinos, Ryan Kirk, E J French, Randall McCallian, Dustin F. Baker
Publikováno v:
Psychopharmacology. 238:1133-1140
Fragile X syndrome (FXS), the most prevalent genetic form of intellectual disability, is characterized by intellectual impairment, impaired sociability, aggression, self-injury, hyperactivity, and attention deficits. A consequence of the hyperactivit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c04512eea9b1f64be503894367229c7f
https://doi.org/10.1007/s00213-021-05760-8
https://doi.org/10.1007/s00213-021-05760-8
Autor:
Ball, Evan R., Caniglia, Mary Kay, Wilcox, Jenna L., Overton, Karla A., Burr, Marra J., Wolfe, Brady D., Sanders, Brian J., Wisniewski, Amy B., Wrenn, Craige C.
Publikováno v:
In Hormones and Behavior 2010 57(3):313-322
Autor:
Craige C, Wrenn, Eric, French, Dustin, Baker, Randall, McCallian, Ryan, Kirk, Mark P, Reilly, Maria G, Valdovinos
Publikováno v:
Psychopharmacology. 238(4)
Fragile X syndrome (FXS), the most prevalent genetic form of intellectual disability, is characterized by intellectual impairment, impaired sociability, aggression, self-injury, hyperactivity, and attention deficits. A consequence of the hyperactivit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e1fe8a181121ed9c4e847fb1ada9caec
https://pubmed.ncbi.nlm.nih.gov/33449137
https://pubmed.ncbi.nlm.nih.gov/33449137
Autor:
Rustay, Nathan R., Wrenn, Craige C., Kinney, Jefferson W., Holmes, Andrew, Bailey, Kathleen R., Sullivan, Timothy L., Harris, Ashley P., Long, Katharine C., Saavedra, Maria C., Starosta, Grzegorz, Innerfield, Caitlin E., Yang, Rebecca J., Dreiling, Jennifer L., Crawley, Jacqueline N.
Publikováno v:
In Neuropeptides 2005 39(3):239-243
Publikováno v:
Alzheimer's & Dementia. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1b6736cadf3dda89e995130ebb45655
https://doi.org/10.1016/j.jalz.2018.06.082
https://doi.org/10.1016/j.jalz.2018.06.082
Publikováno v:
Alzheimer's & Dementia. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53fb254ccdc80cefe0343316d72c5ce0
https://doi.org/10.1016/j.jalz.2018.07.047
https://doi.org/10.1016/j.jalz.2018.07.047
Publikováno v:
Neuroscience Letters. 585:109-113
Fragile X syndrome (FXS), a disorder caused by a mutation in the FMR1 gene, is often associated with Attention Deficit Hyperactivity Disorder (ADHD). Common treatments for the hyperactivity often seen in ADHD involve the use of stimulants and α2-adr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb08008106293c568dae22784d748596
https://doi.org/10.1016/j.neulet.2014.11.035
https://doi.org/10.1016/j.neulet.2014.11.035
Publikováno v:
In Progress in Neuropsychopharmacology & Biological Psychiatry 2001 25(1):283-299