K
Kirrie J. Ballard
Researcher at University of Sydney
Publications - 153
Citations - 4951
Kirrie J. Ballard is an academic researcher from University of Sydney. The author has contributed to research in topics: Apraxia & Aphasia. The author has an hindex of 36, co-authored 138 publications receiving 4107 citations. Previous affiliations of Kirrie J. Ballard include Texas A&M University at Qatar & University of Iowa.
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Journal ArticleDOI
Principles of Motor Learning in Treatment of Motor Speech Disorders
Edwin Maas,Donald A. Robin,Shannon N. Austermann Hula,Skott E. Freedman,Gabriele Wulf,Kirrie J. Ballard,Richard A. Schmidt +6 more
TL;DR: Evidence from nonspeech motor learning suggests that various principles may interact with each other and differentially affect diverse aspects of movements, and available evidence suggests that these principles hold promise for treatment of motor speech disorders.
Journal ArticleDOI
Subtypes of progressive aphasia: application of the International Consensus Criteria and validation using β-amyloid imaging.
Cristian E. Leyton,Victor L. Villemagne,Sharon Savage,Kerryn E. Pike,Kerryn E. Pike,Kirrie J. Ballard,Olivier Piguet,Olivier Piguet,James R. Burrell,James R. Burrell,Christopher C. Rowe,John R. Hodges,John R. Hodges +12 more
TL;DR: Insight is offered into the biological basis of clinical manifestations of Alzheimer's disease, which appear topographically independent of β-amyloid load and can be applied to the majority of cases with primary progressive aphasic using a simple speech and language assessment scale based upon four key variables.
Journal ArticleDOI
Speech, Prosody, and Voice Characteristics of a Mother and Daughter With a 7;13 Translocation Affecting FOXP2
Lawrence D. Shriberg,Kirrie J. Ballard,J. Bruce Tomblin,Joseph R. Duffy,Katharine H. Odell,Charles A. Williams +5 more
TL;DR: Describing the speech, prosody, and voice characteristics of a mother and daughter with a breakpoint in a balanced 7;13 chromosomal translocation that disrupted the transcription gene, FOXP2 supported the conclusion that both mother anddaughter had spastic dysarthria, an apraxia of speech, and residual developmental distortion errors.
Journal ArticleDOI
Differential Diagnosis of Children with Suspected Childhood Apraxia of Speech
TL;DR: Polysyllabic production accuracy and an oral motor examination that includes diadochokinesis may be sufficient to reliably identify CAS and rule out structural abnormality or dysarthria.
Journal ArticleDOI
Patterns of language decline in non-fluent primary progressive aphasia
TL;DR: In this paper, language samples collected yearly for up to 11 years post-onset of symptoms from four subjects presenting with non-fluent primary progressive aphasia (PPA) were analyzed and compared with samples collected from both non-brain-damaged subjects and those with agrammatic Broca's Aphasia resulting from a single left-hemisphere stroke.