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Movement Disorders : Official Journal of the Movement Disorder Society
|
October 10, 2013
Persistent figure-eight and side-to-side head shaking is a marker for rhombencephalosynapsis
Hannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Developmental Medicine and Child Neurology
|
August 29, 2012
ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia
Allison Brashear, Jonathan W Mink, Deborah F Hill, et al.
Research Square
|
August 30, 2023
Assessing the integrity of auditory sensory memory processing in CLN<i>3</i> disease (Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)): An auditory evoked potential study of the duration-evoked mismatch negativity (MMN)
Tufikameni Brima, Edward G Freedman, Kevin D Prinsloo, et al.
Journal of Neurodevelopmental Disorders
|
January 5, 2024
Assessing the integrity of auditory sensory memory processing in CLN3 disease (Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)): an auditory evoked potential study of the duration-evoked mismatch negativity (MMN)
Tufikameni Brima, Edward G Freedman, Kevin D Prinsloo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 25, 2004
Effect of stimulation frequency on tremor suppression in essential tremor
Mwiza Ushe, Jonathan W Mink, Fredy J Revilla, et al.
Pediatric Neurology
|
February 8, 2020
Tic Disorders are Associated With Lower Child and Parent Quality of Life and Worse Family Functioning
Jennifer Vermilion, Erika Augustine, Heather R Adams, et al.
Depression and Anxiety
|
February 26, 2015
SUICIDAL THOUGHTS AND BEHAVIORS IN CHILDREN AND ADOLESCENTS WITH CHRONIC TIC DISORDERS
Eric A Storch, Camille E Hanks, Jonathan W Mink, et al.
Frontiers in Neurology
|
May 7, 2026
Diagnostic approach to episodic ataxia types 1 and 2: a proposed algorithm for limited resource-settings
Claudio M de Gusmao, Lucas H M R Garcia, Jonathan W Mink, et al.
Developmental Medicine and Child Neurology
|
March 2, 2010
Genotype does not predict severity of behavioural phenotype in juvenile neuronal ceroid lipofuscinosis (Batten disease)
Heather R Adams, Christopher A Beck, Erika Levy, et al.
Contemporary Clinical Trials
|
May 1, 2013
Methodology of clinical research in rare diseases: development of a research program in juvenile neuronal ceroid lipofuscinosis (JNCL) via creation of a patient registry and collaboration with patient advocates
Elisabeth A de Blieck, Erika F Augustine, Frederick J Marshall, et al.
Page
of 18
Search research articles
Search
Showing results (131-140 of 171) with videos related to
Sort By:
Page
of 18
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 10, 2013
Persistent figure-eight and side-to-side head shaking is a marker for rhombencephalosynapsis
Hannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Developmental Medicine and Child Neurology
|
August 29, 2012
ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia
Allison Brashear, Jonathan W Mink, Deborah F Hill, et al.
Research Square
|
August 30, 2023
Assessing the integrity of auditory sensory memory processing in CLN<i>3</i> disease (Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)): An auditory evoked potential study of the duration-evoked mismatch negativity (MMN)
Tufikameni Brima, Edward G Freedman, Kevin D Prinsloo, et al.
Journal of Neurodevelopmental Disorders
|
January 5, 2024
Assessing the integrity of auditory sensory memory processing in CLN3 disease (Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)): an auditory evoked potential study of the duration-evoked mismatch negativity (MMN)
Tufikameni Brima, Edward G Freedman, Kevin D Prinsloo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 25, 2004
Effect of stimulation frequency on tremor suppression in essential tremor
Mwiza Ushe, Jonathan W Mink, Fredy J Revilla, et al.
Pediatric Neurology
|
February 8, 2020
Tic Disorders are Associated With Lower Child and Parent Quality of Life and Worse Family Functioning
Jennifer Vermilion, Erika Augustine, Heather R Adams, et al.
Depression and Anxiety
|
February 26, 2015
SUICIDAL THOUGHTS AND BEHAVIORS IN CHILDREN AND ADOLESCENTS WITH CHRONIC TIC DISORDERS
Eric A Storch, Camille E Hanks, Jonathan W Mink, et al.
Frontiers in Neurology
|
May 7, 2026
Diagnostic approach to episodic ataxia types 1 and 2: a proposed algorithm for limited resource-settings
Claudio M de Gusmao, Lucas H M R Garcia, Jonathan W Mink, et al.
Developmental Medicine and Child Neurology
|
March 2, 2010
Genotype does not predict severity of behavioural phenotype in juvenile neuronal ceroid lipofuscinosis (Batten disease)
Heather R Adams, Christopher A Beck, Erika Levy, et al.
Contemporary Clinical Trials
|
May 1, 2013
Methodology of clinical research in rare diseases: development of a research program in juvenile neuronal ceroid lipofuscinosis (JNCL) via creation of a patient registry and collaboration with patient advocates
Elisabeth A de Blieck, Erika F Augustine, Frederick J Marshall, et al.
Page
of 18