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Hits 1 – 20 of 61
1
Assessing agrammatic aphasia (Dyson et al., 2022) ...
Dyson, Bronwen
;
Håkansson, Gisela
;
Ballard, Kirrie J.
. - : ASHA journals, 2022
BASE
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2
Assessing agrammatic aphasia (Dyson et al., 2022) ...
Dyson, Bronwen
;
Håkansson, Gisela
;
Ballard, Kirrie J.
. - : ASHA journals, 2022
BASE
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3
Differential Diagnosis of Childhood Apraxia of Speech Compared to Other Speech Sound Disorders: A Systematic Review
Murray, Elizabeth
;
Iuzzini-Seigel, Jenya
;
Maas, Edwin
...
In: Speech Pathology and Audiology Faculty Research and Publications (2021)
BASE
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4
An Automated Lexical Stress Classification Tool for Assessing Dysprosody in Childhood Apraxia of Speech
McKechnie, Jacqueline
;
Shahin, Mostafa
;
Ahmed, Beena
...
In: Brain Sci (2021)
BASE
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5
Variables Associated with Self-reported Language Impairment in Multiple Sclerosis: A Regression Analysis
El-Wahsh, Sarah
;
Heard, Rob
;
Bogaardt, Hans
...
In: Int J MS Care (2021)
BASE
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6
AusKidTalk : an auditory-visual corpus of 3- to 12-year-old Australian children's speech
Ahmed, Beena
;
Ballard, Kirrie J.
;
Burnham, Denis K.
(R7357). - : France, International Speech and Communication Association, 2021
BASE
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7
Review of diagnosis of childhood apraxia of speech (Murray et al., 2020) ...
Murray, Elizabeth
;
Iuzzini-Seigel, Jenya
;
Maas, Edwin
. - : ASHA journals, 2020
BASE
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8
Review of diagnosis of childhood apraxia of speech (Murray et al., 2020) ...
Murray, Elizabeth
;
Iuzzini-Seigel, Jenya
;
Maas, Edwin
. - : ASHA journals, 2020
BASE
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9
Resting-State Functional Magnetic Resonance Imaging Connectivity Between Semantic and Phonological Regions of Interest May Inform Language Targets in Aphasia
Ramage, Amy E.
;
Aytur, Semra
;
Ballard, Kirrie J.
In: J Speech Lang Hear Res (2020)
BASE
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10
Supporting Children With Speech Sound Disorders During COVID-19 Restrictions: Technological Solutions
McGill, Nicole
;
McLeod, Sharynne
;
Ballard, Kirrie J.
. - 2020
BASE
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11
Common and divergent neural correlates of anomia in amnestic and logopenic presentations of Alzheimer's disease
Piguet, Olivier
;
Leyton, Cristian E
;
Hodges, John R
. - : Elsevier, 2017
BASE
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12
A Predictive model for diagnosing stroke-related apraxia of speech
Ballard, Kirrie J
;
Azizi, Lamiae
;
Duffy, Joseph R
. - : Elsevier, 2016
BASE
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13
Syntactic comprehension deficits across the FTD-ALS continuum
Kamminga, Jody
;
Leslie, Felicity V.C.
;
Hsieh, Sharpley
. - 2016
BASE
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14
Cognitive, Linguistic, and Motor Abilities in a Multigenerational Family with Childhood Apraxia of Speech
Carrigg, Bronwyn
;
Parry, Louise
;
Baker, Elise
...
In: Arch Clin Neuropsychol (2016)
BASE
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15
Cognitive, linguistic, and motor abilities in a multigenerational family with childhood apraxia of speech
Carrigg, Bronwyn
;
Parry, Louise
;
Baker, Elise
(R20118);
Shriberg, Lawrence D.
;
Ballard, Kirrie J.
. - : U.K., Oxford University Press, 2016
Abstract:
Objective: This study describes the phenotype in a large family with a strong, multigenerational history of severe speech sound disorder (SSD) persisting into adolescence and adulthood in approximately half the cases. Aims were to determine whether a core phenotype, broader than speech, separated persistent from resolved SSD cases; and to ascertain the uniqueness of the phenotype relative to published cases. Method: Eleven members of the PM family (9–55 years) were assessed across cognitive, language, literacy, speech, phonological processing, numeracy, and motor domains. Between group comparisons were made using the Mann–Whitney U-test (p < 0.01). Participant performances were compared to normative data using standardized tests and to the limited published data on persistent SSD phenotypes. Results: Significant group differences were evident on multiple speech, language, literacy, phonological processing, and verbal intellect measures without any overlapping scores. Persistent cases performed within the impaired range on multiple measures. Phonological memory impairment and subtle literacy weakness were present in resolved SSD cases. Conclusion: A core phenotype distinguished persistent from resolved SSD cases that was characterized by a multiple verbal trait disorder, including Childhood Apraxia of Speech. Several phenotypic differences differentiated the persistent SSD phenotype in the PM family from the few previously reported studies of large families with SSD, including the absence of comorbid dysarthria and marked orofacial apraxia. This study highlights how comprehensive phenotyping can advance the behavioral study of disorders, in addition to forming a solid basis for future genetic and neural studies.
Keyword:
apraxia
;
children
;
phenotype
;
speech
;
speech disorders
;
XXXXXX - Unknown
URL:
https://hdl.handle.net/1959.7/uws:55279
https://doi.org/10.1093/arclin/acw077
BASE
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16
Treatment for acquired apraxia of speech : a systematic review of intervention research between 2004 and 2012
Ballard, Kirrie J
;
Wambaugh, Julie L
;
Duffy, Joseph R
. - : American Speech-Language-Hearing Association, 2015
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17
Persistent speech sound disorder in a 22-year-old male : communication, educational, socio-emotional, and vocational outcomes
Carrigg, Bronwyn
;
Baker, Elise
(R20118);
Parry, Louise
. - : U.S., American Speech - Language - Hearing Association, 2015
BASE
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18
An acoustic measure of lexical stress differentiates aphasia and aphasia plus apraxia of speech after stroke
Vergis, Marianne K.
;
Ballard, Kirrie J.
;
Duffy, Joseph R.
...
In:
Aphasiology. - London [u.a.] : Routledge, Taylor & Francis Group
28 (2014) 5, 554-575
OLC Linguistik
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19
Phonological encoding in apraxia of speech and aphasia
Maas, Edwin
;
Gutirrez, Keila
;
Ballard, Kirrie J.
In:
Aphasiology. - London [u.a.] : Routledge, Taylor & Francis Group
28 (2014) 1, 25-48
OLC Linguistik
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20
Rapid Syllable Transitions (ReST) treatment for Childhood Apraxia of Speech: The effect of lower dose-Frequency
Thomas, Donna C.
;
McCabe, Patricia
;
Ballard, Kirrie J.
In:
Journal of communication disorders. - New York, NY : Elsevier
51 (2014), 29-42
OLC Linguistik
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