Below are the most recent publications written about "Speech Disorders" by people in Profiles.
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Ukaegbe OC, Holt BE, Keator LM, Brownell H, Blake ML, Lundgren K. Aprosodia Following Focal Brain Damage: What's Right and What's Left? Am J Speech Lang Pathol. 2022 Oct 25; 31(5S):2313-2328.
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Sheppard SM, Stockbridge MD, Keator LM, Murray LL, Blake ML. The Company Prosodic Deficits Keep Following Right Hemisphere Stroke: A Systematic Review. J Int Neuropsychol Soc. 2022 11; 28(10):1075-1090.
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Stockbridge MD, Sheppard SM, Keator LM, Murray LL, Lehman Blake M. Aprosodia Subsequent to Right Hemisphere Brain Damage: A Systematic Review and Meta-Analysis - CORRIGENDUM. J Int Neuropsychol Soc. 2022 10; 28(9):996.
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Mailend ML, Maas E, Story BH. Apraxia of speech and the study of speech production impairments: Can we avoid further confusion? Reply to Romani (2021). Cogn Neuropsychol. 2021 May-Jun; 38(4):309-317.
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Stockbridge MD, Sheppard SM, Keator LM, Murray LL, Lehman Blake M. Aprosodia Subsequent to Right Hemisphere Brain Damage: A Systematic Review and Meta-Analysis. J Int Neuropsychol Soc. 2022 08; 28(7):709-735.
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Mailend ML, Maas E, Beeson PM, Story BH, Forster KI. Examining speech motor planning difficulties in apraxia of speech and aphasia via the sequential production of phonetically similar words. Cogn Neuropsychol. 2021 02; 38(1):72-87.
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Mailend ML, Maas E, Beeson PM, Story BH, Forster KI. Speech motor planning in the context of phonetically similar words: Evidence from apraxia of speech and aphasia. Neuropsychologia. 2019 04; 127:171-184.
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Daggumati S, Cohn JE, Brennan MJ, Evarts M, McKinnon BJ, Terk AR. Caregiver perception of speech quality in patients with ankyloglossia: Comparison between surgery and non-treatment. Int J Pediatr Otorhinolaryngol. 2019 Apr; 119:70-74.
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Zou F, McWalter K, Schmidt L, Decker A, Picker JD, Lincoln S, Sweetser DA, Briere LC, Harini C, Marsh E, Medne L, Wang RY, Leydiker K, Mower A, Visser G, Cuppen I, van Gassen KL, van der Smagt J, Yousaf A, Tennison M, Shanmugham A, Butler E, Richard G, McKnight D. Expanding the phenotypic spectrum of GABRG2 variants: a recurrent GABRG2 missense variant associated with a severe phenotype. J Neurogenet. 2017 Mar - Jun; 31(1-2):30-36.
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Reuter MS, Riess A, Moog U, Briggs TA, Chandler KE, Rauch A, Stampfer M, Steindl K, Gl?ser D, Joset P, Krumbiegel M, Rabe H, Schulte-Mattler U, Bauer P, Beck-W?dl S, Kohlhase J, Reis A, Zweier C. FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. J Med Genet. 2017 01; 54(1):64-72.