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Samantha J Turner

Showing results (1-10 of 21) with videos related to

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Current Neurology and Neuroscience Reports|April 30, 2015
New genes for focal epilepsies with speech and language disordersSamantha J Turner, Angela T Morgan, Eliane Roulet Perez, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 2005
Shear induces a unique series of morphological changes in translocating platelets: effects of morphology on translocation dynamicsMhairi J Maxwell, Sacha M Dopheide, Samantha J Turner, et al.
Current Neurology and Neuroscience Reports|June 23, 2015
Erratum to: New Genes for Focal Epilepsies with Speech and Language DisordersSamantha J Turner, Angela T Morgan, Eliane Roulet Perez, et al.
Neurology|February 3, 2017
Dysarthria and broader motor speech deficits in Dravet syndromeSamantha J Turner, Amy Brown, Marta Arpone, et al.
Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|July 23, 2019
Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of SpeechSamantha J Turner, Adam P Vogel, Bronwyn Parry-Fielder, et al.
Neurology|January 18, 2015
GRIN2A: an aptly named gene for speech dysfunctionSamantha J Turner, Angela K Mayes, Andrea Verhoeven, et al.
Epilepsia|January 9, 2013
Clinical genetic study of the epilepsy-aphasia spectrumMeng-Han Tsai, Danya F Vears, Samantha J Turner, et al.
Scientific Reports|October 14, 2016
Early neuroimaging markers of FOXP2 intragenic deletionFrédérique J Liégeois, Michael S Hildebrand, Alexandra Bonthrone, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthriaSamantha J Turner, Michael S Hildebrand, Susan Block, et al.
Neurology. Genetics|May 8, 2024
Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic <i>GRIN2A</i> VariantsDaisy G Y Thompson-Lake, Frederique J Liegeois, Ruth O Braden, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Current Neurology and Neuroscience Reports|April 30, 2015
New genes for focal epilepsies with speech and language disordersSamantha J Turner, Angela T Morgan, Eliane Roulet Perez, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 2005
Shear induces a unique series of morphological changes in translocating platelets: effects of morphology on translocation dynamicsMhairi J Maxwell, Sacha M Dopheide, Samantha J Turner, et al.
Current Neurology and Neuroscience Reports|June 23, 2015
Erratum to: New Genes for Focal Epilepsies with Speech and Language DisordersSamantha J Turner, Angela T Morgan, Eliane Roulet Perez, et al.
Neurology|February 3, 2017
Dysarthria and broader motor speech deficits in Dravet syndromeSamantha J Turner, Amy Brown, Marta Arpone, et al.
Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|July 23, 2019
Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of SpeechSamantha J Turner, Adam P Vogel, Bronwyn Parry-Fielder, et al.
Neurology|January 18, 2015
GRIN2A: an aptly named gene for speech dysfunctionSamantha J Turner, Angela K Mayes, Andrea Verhoeven, et al.
Epilepsia|January 9, 2013
Clinical genetic study of the epilepsy-aphasia spectrumMeng-Han Tsai, Danya F Vears, Samantha J Turner, et al.
Scientific Reports|October 14, 2016
Early neuroimaging markers of FOXP2 intragenic deletionFrédérique J Liégeois, Michael S Hildebrand, Alexandra Bonthrone, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthriaSamantha J Turner, Michael S Hildebrand, Susan Block, et al.
Neurology. Genetics|May 8, 2024
Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic <i>GRIN2A</i> VariantsDaisy G Y Thompson-Lake, Frederique J Liegeois, Ruth O Braden, et al.
Pageof 3