Brysbaert M, Stevens M, Mandera P, Keuleers E The impact of word prevalence on lexical decision times: Evidence from the Dutch Lexicon Project 2. J Exp Psychol Hum Percept Perform. 2016 Mar;42(3):441-58. doi: 10.1037/xhp0000159. Epub 2015 Oct 26.
DE RENZI E, VIGNOLO LA The token test: A sensitive test to detect receptive disturbances in aphasics. Brain. 1962 Dec;85:665-78. doi: 10.1093/brain/85.4.665. No abstract available.
Dell GS, Martin N, Schwartz MF A Case-Series Test of the Interactive Two-step Model of Lexical Access: Predicting Word Repetition from Picture Naming. J Mem Lang. 2007 May 1;56(4):490-520. doi: 10.1016/j.jml.2006.05.007.
Dell GS, O'Seaghdha PG Stages of lexical access in language production. Cognition. 1992 Mar;42(1-3):287-314. doi: 10.1016/0010-0277(92)90046-k.
Harnish SM, Lundine JP Nonverbal Working Memory as a Predictor of Anomia Treatment Success. Am J Speech Lang Pathol. 2015 Nov;24(4):S880-94. doi: 10.1044/2015_AJSLP-14-0153.
Ivanova MV, Hallowell B A tutorial on aphasia test development in any language: Key substantive and psychometric considerations. Aphasiology. 2013 Jan 1;27(8):891-920. doi: 10.1080/02687038.2013.805728.
Kay, J, Lesser, R, Coltheart, M Psycholinguistic assessments of language processing in aphasia (PALPA): An introduction. Aphasiology. 1996; 10(2): 159-180.
Lang CJ, Quitz A Verbal and nonverbal memory impairment in aphasia. J Neurol. 2012 Aug;259(8):1655-61. doi: 10.1007/s00415-011-6394-1. Epub 2012 Jan 19.
Martin N, Gupta P Exploring the relationship between word processing and verbal short-term memory: evidence from associations and dissociations. Cogn Neuropsychol. 2004 Mar 1;21(2):213-28. doi: 10.1080/02643290342000447.
Martin N, Minkina I, Kohen FP, Kalinyak-Fliszar M Assessment of linguistic and verbal short-term memory components of language abilities in aphasia. J Neurolinguistics. 2018 Nov;48:199-225. doi: 10.1016/j.jneuroling.2018.02.006.
Mayer JF, Murray LL Measuring working memory deficits in aphasia. J Commun Disord. 2012 Sep-Oct;45(5):325-39. doi: 10.1016/j.jcomdis.2012.06.002. Epub 2012 Jun 16.
McNeil, MR, Pratt, SR Defining aphasia: Some theoretical and clinical implications of operating from a formal definition. Aphasiology. 2001; 15(10-11): 901-911.
Murray L, Salis C, Martin N, Dralle J The use of standardised short-term and working memory tests in aphasia research: a systematic review. Neuropsychol Rehabil. 2018 Apr;28(3):309-351. doi: 10.1080/09602011.2016.1174718. Epub 2016 May 4.
Murray, LL Direct and indirect treatment approaches for addressing short-term or working memory deficits in aphasia. Aphasiology. 2012; 26(3-4): 317-337.
Seniow J, Litwin M, Lesniak M The relationship between non-linguistic cognitive deficits and language recovery in patients with aphasia. J Neurol Sci. 2009 Aug 15;283(1-2):91-4. doi: 10.1016/j.jns.2009.02.315. Epub 2009 Mar 6.
Towards a Clinical Test Battery for the Assessment of Verbal Short-term Memory Abilities With Linguistic Variations in Patients With Poststroke Aphasia.
Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.
Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.
Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.
Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.
Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.