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Jonathan P. Dyke

Researcher at Cornell University

Publications -  146
Citations -  5769

Jonathan P. Dyke is an academic researcher from Cornell University. The author has contributed to research in topics: Magnetic resonance imaging & Medicine. The author has an hindex of 36, co-authored 126 publications receiving 4821 citations. Previous affiliations of Jonathan P. Dyke include Memorial Sloan Kettering Cancer Center & University of Tennessee.

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Treatment of late infantile neuronal ceroid lipofuscinosis by CNS administration of a serotype 2 adeno-associated virus expressing CLN2 cDNA.

TL;DR: Assessment of the primary outcome variable suggests a slowing of progression of LINCL in the treated children, and it is proposed that additional studies to assess the safety and efficacy of AAV-mediated gene therapy for LINCL are warranted.
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Study of Intraventricular Cerliponase Alfa for CLN2 Disease.

TL;DR: Intraventricular infusion of cerliponase alfa in patients with CLN2 disease resulted in less decline in motor and language function than that in historical controls.
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Possible axonal regrowth in late recovery from the minimally conscious state.

TL;DR: It is proposed that axonal regrowth may underlie these findings and provide a biological mechanism for late recovery and is discussed in the context of recent experimental studies that support this inference.
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The Medial Prefrontal Cortex and the Emergence of Self-Conscious Emotion in Adolescence

TL;DR: Findings demonstrate that adolescents’ self-consciousness is related to age-dependent sensitivity of brain systems critical to socioaffective processes, and unique interactions between the MPFC and striatum may provide a mechanism by which social-evaluation contexts influence adolescent behavior.
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Dissociations between behavioural and functional magnetic resonance imaging-based evaluations of cognitive function after brain injury

TL;DR: Observations reveal significant challenges in developing validated functional magnetic resonance imaging-based methods for clinical use and raise interesting questions about underlying brain function assayed using these methods in brain-injured subjects.