Search Results - "Jakielski, Kathy" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

by Eising, Else, Carrion-Castillo, Amaia, Vino, Arianna, Strand, Edythe A., Jakielski, Kathy J., Scerri, Thomas S., Hildebrand, Michael S., Webster, Richard, Ma, Alan, Mazoyer, Bernard, Francks, Clyde, Bahlo, Melanie, Scheffer, Ingrid E., Morgan, Angela T., Shriberg, Lawrence D., Fisher, Simon E.
Published in Molecular psychiatry (01.07.2019)

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Estimates of the prevalence of speech and motor speech disorders in persons with complex neurodevelopmental disorders

Estimates of the prevalence of speech and motor speech disorders in persons with complex neurodevelopmental disorders

by Shriberg, Lawrence D., Strand, Edythe A., Jakielski, Kathy J., Mabie, Heather L.
Published in Clinical linguistics & phonetics (03.08.2019)

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A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: I. Development and Description of the Pause Marker

A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: I. Development and Description of the Pause Marker

by Shriberg, Lawrence D, Strand, Edythe A, Fourakis, Marios, Jakielski, Kathy J, Hall, Sheryl D, Karlsson, Heather B, Mabie, Heather L, McSweeny, Jane L, Tilkens, Christie M, Wilson, David L
Published in Journal of speech, language, and hearing research (01.04.2017)

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Encoding, Memory, and Transcoding Deficits in Childhood Apraxia of Speech

Encoding, Memory, and Transcoding Deficits in Childhood Apraxia of Speech

by Shriberg, Lawrence D, Lohmeier, Heather L, Strand, Edythe A, Jakielski, Kathy J
Published in Clinical linguistics & phonetics (01.05.2012)

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A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: III. Theoretical Coherence of the Pause Marker with Speech Processing Deficits in Childhood Apraxia of Speech

A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: III. Theoretical Coherence of the Pause Marker with Speech Processing Deficits in Childhood Apraxia of Speech

by Shriberg, Lawrence D, Strand, Edythe A, Fourakis, Marios, Jakielski, Kathy J, Hall, Sheryl D, Karlsson, Heather B, Mabie, Heather L, McSweeny, Jane L, Tilkens, Christie M, Wilson, David L
Published in Journal of speech, language, and hearing research (01.04.2017)

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A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: II. Validity Studies of the Pause Marker

A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: II. Validity Studies of the Pause Marker

by Shriberg, Lawrence D, Strand, Edythe A, Fourakis, Marios, Jakielski, Kathy J, Hall, Sheryl D, Karlsson, Heather B, Mabie, Heather L, McSweeny, Jane L, Tilkens, Christie M, Wilson, David L
Published in Journal of speech, language, and hearing research (01.04.2017)

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Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization

Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization

by Laffin, Jennifer J.S., Raca, Gordana, Jackson, Craig A., Strand, Edythe A., Jakielski, Kathy J., Shriberg, Lawrence D.
Published in Genetics in medicine (01.11.2012)

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Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome

Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome

by Raca, Gordana, Baas, Becky S, Kirmani, Salman, Laffin, Jennifer J, Jackson, Craig A, Strand, Edythe A, Jakielski, Kathy J, Shriberg, Lawrence D
Published in European journal of human genetics : EJHG (01.04.2013)

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A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: IV. the Pause Marker Index

A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: IV. the Pause Marker Index

by Shriberg, Lawrence D, Strand, Edythe A, Fourakis, Marios, Jakielski, Kathy J, Hall, Sheryl D, Karlsson, Heather B, Mabie, Heather L, McSweeny, Jane L, Tilkens, Christie M, Wilson, David L
Published in Journal of speech, language, and hearing research (01.04.2017)

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A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: Introduction

A Diagnostic Marker to Discriminate Childhood Apraxia of Speech from Speech Delay: Introduction

by Shriberg, Lawrence D, Strand, Edythe A, Fourakis, Marios, Jakielski, Kathy J, Hall, Sheryl D, Karlsson, Heather B, Mabie, Heather L, McSweeny, Jane L, Tilkens, Christie M, Wilson, David L
Published in Journal of speech, language, and hearing research (01.04.2017)

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Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech

by Worthey, Elizabeth A, Raca, Gordana, Laffin, Jennifer J, Wilk, Brandon M, Harris, Jeremy M, Jakielski, Kathy J, Dimmock, David P, Strand, Edythe A, Shriberg, Lawrence D
Published in Journal of neurodevelopmental disorders (02.10.2013)

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Phenotype of FOXP2 haploinsufficiency in a mother and son

Phenotype of FOXP2 haploinsufficiency in a mother and son

by Rice, Gregory M., Raca, Gordana, Jakielski, Kathy J., Laffin, Jennifer J., Iyama‐Kurtycz, Christina M., Hartley, Sigan L., Sprague, Rae E., Heintzelman, Anne T., Shriberg, Lawrence D.
Published in American journal of medical genetics. Part A (01.01.2012)

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Motor-Based Intervention Protocols in Treatment of Childhood Apraxia of Speech (CAS)

Motor-Based Intervention Protocols in Treatment of Childhood Apraxia of Speech (CAS)

by Maas, E., Gildersleeve-Neumann, C. E., Jakielski, K. J., Stoeckel, R.
Published in Current developmental disorders reports (01.09.2014)

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Breakpoint localization using array-CGH in three siblings with an unbalanced 4q;16q translocation and childhood apraxia of speech (CAS)

Breakpoint localization using array-CGH in three siblings with an unbalanced 4q;16q translocation and childhood apraxia of speech (CAS)

by Shriberg, Lawrence D., Jakielski, Kathy J., El-Shanti, Hatem
Published in American journal of medical genetics. Part A (01.09.2008)

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The Making of a Speech Scientist: Intrigued by an apraxia study, a 13-year-old seeks a researcher’s help for a middle school science fair project

The Making of a Speech Scientist: Intrigued by an apraxia study, a 13-year-old seeks a researcher’s help for a middle school science fair project

by Jakielski, Kathy J
Published in ASHA leader (01.11.2018)

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A single case experimental design study using an operationalised version of the Kaufman Speech to Language Protocol for children with childhood apraxia of speech

A single case experimental design study using an operationalised version of the Kaufman Speech to Language Protocol for children with childhood apraxia of speech

by Gomez, Maryane, Purcell, Alison, Jakielski, Kathy, McCabe, Patricia
Published in International journal of speech language pathology (01.04.2024)

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Bang for Your Buck: A Single-Case Experimental Design Study of Practice Amount and Distribution in Treatment for Childhood Apraxia of Speech

Bang for Your Buck: A Single-Case Experimental Design Study of Practice Amount and Distribution in Treatment for Childhood Apraxia of Speech

by Maas, Edwin, Gildersleeve-Neumann, Christina, Jakielski, Kathy, Kovacs, Nicolette, Stoeckel, Ruth, Vradelis, Helen, Welsh, Mackenzie
Published in Journal of speech, language, and hearing research (01.09.2019)

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Treating Childhood Apraxia of Speech with the Kaufman Speech to Language Protocol: A Phase I Pilot Study

Treating Childhood Apraxia of Speech with the Kaufman Speech to Language Protocol: A Phase I Pilot Study

by Gomez, Maryane, McCabe, Patricia, Jakielski, Kathy, Purcell, Alison
Published in Language, speech & hearing services in schools (01.07.2018)

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The Making of a Speech Scientist

The Making of a Speech Scientist

by Jakielski, Kathy J
Published in ASHA Leader (01.11.2018)

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Trade Publication Article

Phenotype of FOXP2 haploinsufficiency in a mother and son

Phenotype of FOXP2 haploinsufficiency in a mother and son

by Rice, Gregory M., Raca, Gordana, Jakielski, Kathy J., Laffin, Jennifer J., Iyama-Kurtycz, Christina M., Hartley, Sigan L., Sprague, Rae E., Heintzelman, Anne T., Shriberg, Lawrence D.
Published in American Journal of Medical Genetics Part A (01.01.2012)

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