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Lance H Rodan

Showing results (21-30 of 76) with videos related to

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Journal of Child Neurology|October 5, 2013
Anti-glutamic Acid decarboxylase antibody associated limbic encephalitis in a child: expanding the spectrum of pediatric inflammatory brain diseasesNavin Mishra, Lance H Rodan, Dragos A Nita, et al.
European Journal of Human Genetics : EJHG|June 23, 2016
A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin geneLance H Rodan, Julie Cohen, Ali Fatemi, et al.
Movement Disorders Clinical Practice|August 9, 2019
VAC14 Gene-Related Parkinsonism-Dystonia With Response to Deep Brain StimulationClaudio M de Gusmao, Scellig Stone, Jeff L Waugh, et al.
Journal of Child Neurology|November 1, 2016
De Novo TUBB2A Variant Presenting With Anterior Temporal PachygyriaLance H Rodan, Christelle Moufawad El Achkar, Gerard T Berry, et al.
Pediatrics|June 3, 2016
A 10-Month-Old With Intermittent Hypotonia and ParalysisBeate C Beinvogl, N Paul Rosman, Fiona M Baumer, et al.
JIMD Reports|September 10, 2017
Liver Failure as the Presentation of Ornithine Transcarbamylase Deficiency in a 13-Month-Old FemaleFarrah Rajabi, Lance H Rodan, Maureen M Jonas, et al.
JIMD Reports|September 14, 2022
Expansion of the clinical and neuroimaging spectrum associated with NDUFS8-related disorderMilena M Andzelm, Shanti Balasubramaniam, Edward Yang, et al.
Annals of Neurology|September 22, 2020
Polymicrogyria is Associated With Pathogenic Variants in PTENDiane D Shao, Christelle M Achkar, Abbe Lai, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
A <i>de novo</i> missense variant in <i>EZH1</i> associated with developmental delay exhibits functional deficits in <i>Drosophila melanogaster</i>Sharayu Jangam, Lauren C Briere, Kristy Jay, et al.
Molecular Genetics and Metabolism|July 23, 2018
5,10-methenyltetrahydrofolate synthetase deficiency causes a neurometabolic disorder associated with microcephaly, epilepsy, and cerebral hypomyelinationLance H Rodan, Wanshu Qi, Gregory S Ducker, et al.
Pageof 8

Showing results (21-30 of 76) with videos related to

Sort By:
Pageof 8
Journal of Child Neurology|October 5, 2013
Anti-glutamic Acid decarboxylase antibody associated limbic encephalitis in a child: expanding the spectrum of pediatric inflammatory brain diseasesNavin Mishra, Lance H Rodan, Dragos A Nita, et al.
European Journal of Human Genetics : EJHG|June 23, 2016
A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin geneLance H Rodan, Julie Cohen, Ali Fatemi, et al.
Movement Disorders Clinical Practice|August 9, 2019
VAC14 Gene-Related Parkinsonism-Dystonia With Response to Deep Brain StimulationClaudio M de Gusmao, Scellig Stone, Jeff L Waugh, et al.
Journal of Child Neurology|November 1, 2016
De Novo TUBB2A Variant Presenting With Anterior Temporal PachygyriaLance H Rodan, Christelle Moufawad El Achkar, Gerard T Berry, et al.
Pediatrics|June 3, 2016
A 10-Month-Old With Intermittent Hypotonia and ParalysisBeate C Beinvogl, N Paul Rosman, Fiona M Baumer, et al.
JIMD Reports|September 10, 2017
Liver Failure as the Presentation of Ornithine Transcarbamylase Deficiency in a 13-Month-Old FemaleFarrah Rajabi, Lance H Rodan, Maureen M Jonas, et al.
JIMD Reports|September 14, 2022
Expansion of the clinical and neuroimaging spectrum associated with NDUFS8-related disorderMilena M Andzelm, Shanti Balasubramaniam, Edward Yang, et al.
Annals of Neurology|September 22, 2020
Polymicrogyria is Associated With Pathogenic Variants in PTENDiane D Shao, Christelle M Achkar, Abbe Lai, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
A <i>de novo</i> missense variant in <i>EZH1</i> associated with developmental delay exhibits functional deficits in <i>Drosophila melanogaster</i>Sharayu Jangam, Lauren C Briere, Kristy Jay, et al.
Molecular Genetics and Metabolism|July 23, 2018
5,10-methenyltetrahydrofolate synthetase deficiency causes a neurometabolic disorder associated with microcephaly, epilepsy, and cerebral hypomyelinationLance H Rodan, Wanshu Qi, Gregory S Ducker, et al.
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