Special Topics:
Speech and Other Neurodevelopmental Disorders

Potter, N., Johnson, J., & Shriberg, L.D. (2006, June). Speech and language characteristics of children with galactosemia. Poster presented at the Symposium on Research in Child Language Disorders, Madison, WI.

Shriberg, L. D. (December, 2008). Comparative Studies in Neurodevelopmental and Idiopathic Childhood Apraxia of Speech (CAS). Paper presented at the Eighth International Speech Production Seminar, Strasbourg, France.

Shriberg, L. D. (March, 2008). Studies of Childhood Apraxia of Speech in complex neurodevelopmental disorders. Paper presented at the Fourteenth Biennial Conference on Motor Speech: Motor Speech Disorders & Speech Motor Control, Monterey, CA.

Bissell, R. & Kwiatkowski, J. (February, 2010). Four-year retrospective speech/language report of a child with Joubert syndrome. Paper presented at the Wisconsin Speech-Language and Hearing Association Annual Convention.

Potter, N. L., Niever, Y., & Shriberg, L. D. (2013). Motor speech disorders in Classic Galactosemia. Journal of Inherited Metabolic Disease Reports. Apr 2 [Epub ahead of print].

Vick, J.C., Campbell, T.C., Shriberg, L.D., Green, J.R., Truemper, K., Rusiewicz, H.L., & Moore, C.A. (2014). Data-driven subclassification of speech sound disorders in preschool children. Journal of Speech, Language, and Hearing Research, 57, 2033-2050.

Shriberg, L. D., Strand, E. A., & Mabie, H. L. (March, 2016). Prevalence estimates for three types of Motor Speech Disorders in Complex Neurodevelopmental Disorders (CND). Paper presented at the Eighteenth Biennial Conference on Motor Speech: Motor Speech Disorders & Speech Motor Control, Newport Beach, CA.

Shriberg, L. D. (July, 2017). Motor Speech Disorder-Not Otherwise Specified: Prevalence and Phenotype. Paper presented at the 7th International Conference on Speech Motor Control, Groningen, the Netherlands.

Baylis, A. L., & Shriberg, L. D. (2018). Estimates of the prevalence of speech and motor speech disorders in youth with 22q11.2 Deletion syndrome. American Journal of Speech-Language Pathology. Advance online publication. doi: 10.1044/2018_AJSLP-18-0037.

Snijders Blok, L., and multiple authors (2018). CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications, 9:4619. DOI: 10.1038/s41467-018-06014-6.

Shriberg, L. D., & Wren, Y. E. (2019). A frequent acoustic sign of Speech Motor Delay (SMD). Clinical Linguistics & Phonetics. doi:10.1080/02699206.2019.1595734. [Epub ahead of print]

Wilson, E. M., Abbeduto, L., Camarata, S. M., & Shriberg, L. D. (2019). Estimates of the prevalence of speech and motor speech disorders in adolescents with Down syndrome. Clinical Linguistics & Phonetics.

Wilson, E. M., Abbeduto, L., Camarata, S. M., & Shriberg, L. D. (2019). Speech and motor speech disorders and intelligibility in adolescents with Down syndrome. Clinical Linguistics & Phonetics.