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

por Shriberg, Lawrence D., Strand, Edythe A., Jakielski, Kathy J., Mabie, Heather L.
Publicado 2019

Orofacial Muscle Strength across the Dysarthrias

por Clark, Heather M., Duffy, Joseph R., Strand, Edythe A., Hanley, Holly, Solomon, Nancy Pearl
Publicado 2022

Western Aphasia Battery–Revised Profiles in Primary Progressive Aphasia and Primary Progressive Apraxia of Speech

por Clark, Heather M., Utianski, Rene L., Duffy, Joseph R., Strand, Edythe A., Botha, Hugo, Josephs, Keith A., Whitwell, Jennifer L.
Publicado 2019

The Apraxia of Speech Rating Scale: Reliability, Validity, and Utility

por Duffy, Joseph R., Martin, Peter R., Clark, Heather M., Utianski, Rene L., Strand, Edythe A., Whitwell, Jennifer L., Josephs, Keith A.
Publicado 2023

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

por 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
Publicado 2013

Characterizing a neurodegenerative syndrome: primary progressive apraxia of speech

por Josephs, Keith A., Duffy, Joseph R., Strand, Edythe A., Machulda, Mary M., Senjem, Matthew L., Master, Ankit V., Lowe, Val J., Jack, Clifford R., Whitwell, Jennifer L.
Publicado 2012

Clinical and MRI models predicting amyloid deposition in progressive aphasia and apraxia of speech

por Whitwell, Jennifer L., Weigand, Stephen D., Duffy, Joseph R., Strand, Edythe A., Machulda, Mary M., Senjem, Matthew L., Gunter, Jeffrey L., Lowe, Val J., Jack, Clifford R., Josephs, Keith A.
Publicado 2016

Disrupted functional connectivity in primary progressive apraxia of speech

por Botha, Hugo, Utianski, Rene L., Whitwell, Jennifer L., Duffy, Joseph R., Clark, Heather M., Strand, Edythe A., Machulda, Mary M., Tosakulwong, Nirubol, Knopman, David S., Petersen, Ronald C., Jack, Clifford R., Josephs, Keith A., Jones, David T.
Publicado 2018

FDG PET and MRI in Logopenic Primary Progressive Aphasia versus Dementia of the Alzheimer’s Type

por Madhavan, Ajay, Whitwell, Jennifer L., Weigand, Stephen D., Duffy, Joseph R., Strand, Edythe A., Machulda, Mary M., Tosakulwong, Nirubol, Senjem, Matthew L., Gunter, Jeffrey L., Lowe, Val J., Petersen, Ronald C., Jack, Clifford R., Josephs, Keith A.
Publicado 2013

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

por 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.
Publicado 2018

Tractography of supplementary motor area projections in progressive speech apraxia and aphasia

por Valls Carbo, Adrian, Reid, Robert I., Tosakulwong, Nirubol, Weigand, Stephen D., Duffy, Joseph R., Clark, Heather M., Utianski, Rene L., Botha, Hugo, Machulda, Mary M., Strand, Edythe A., Schwarz, Christopher G., Jack, Clifford R., Josephs, Keith A., Whitwell, Jennifer L.
Publicado 2022

A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech

por Josephs, Keith A., Duffy, Joseph R., Clark, Heather M., Utianski, Rene L., Strand, Edythe A., Machulda, Mary M., Botha, Hugo, Martin, Peter R., Pham, Nha Trang Thu, Stierwalt, Julie, Ali, Farwa, Buciuc, Marina, Baker, Matthew, Fernandez De Castro, Cristhoper H., Spychalla, Anthony J., Schwarz, Christopher G., Reid, Robert I., Senjem, Matthew L., Jack, Clifford R., Lowe, Val J., Bigio, Eileen H., Reichard, Ross R., Polley, Eric. J., Ertekin-Taner, Nilufer, Rademakers, Rosa, DeTure, Michael A., Ross, Owen A., Dickson, Dennis W., Whitwell, Jennifer L.
Publicado 2021

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

por Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.
Publicado 2018

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

por Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.
Publicado 2019

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

por Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.
Publicado 2019