Biblio

Found 6 results
Filters: Keyword is Mutation  [Clear All Filters]
2020
Burdekin ED, Fogel BL, Jeste SS, Martinez J, Rexach JE, Distefano C, Hyde C, Safari T, Wilson RB.  2020.  The Neurodevelopmental and Motor Phenotype of SCA21 (ATX-TMEM240).. J Child Neurol. 35(14):953-962.
2014
Carpenter KM, Eisenberg S, Weltfreid S, Low CA, Beran T, Stanton AL.  2014.  Characterizing biased cancer-related cognitive processing: relationships with BRCA1/2 genetic mutation status, personal cancer history, age, and prophylactic surgery.. Health Psychol. 33(9):1003-11.
2013
John J, Thannickal TC, McGregor R, Ramanathan L, Ohtsu H, Nishino S, Sakai N, Yamanaka A, Stone C, Cornford M et al..  2013.  Greatly increased numbers of histamine cells in human narcolepsy with cataplexy.. Annals of Neurology. 74(6):786-93.
2011
Wu M-F, Nienhuis R, Maidment N, Lam HA, Siegel JM.  2011.  Role of the hypocretin (orexin) receptor 2 (Hcrt-r2) in the regulation of hypocretin level and cataplexy.. J Neurosci. 31(17):6305-10.
2008
Low CA, Bower JE, Kwan L, Seldon J.  2008.  Benefit finding in response to BRCA1/2 testing.. Ann Behav Med. 35(1):61-9.
Beran TM, Stanton AL, Kwan L, Seldon J, Bower JE, Vodermaier A, Ganz PA.  2008.  The trajectory of psychological impact in BRCA1/2 genetic testing: does time heal? Ann Behav Med. 36(2):107-16.