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Martin Delatycki

Showing results (31-40 of 57) with videos related to

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Stem Cell Research|August 16, 2019
Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum DisorderKiymet Bozaoglu, Yujing Gao, Edouard Stanley, et al.
Brain : a Journal of Neurology|March 5, 2003
Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical courseFerdinando Squitieri, Cinzia Gellera, Milena Cannella, et al.
Annals of Clinical and Translational Neurology|July 2, 2024
Gradient of microstructural damage along the dentato-thalamo-cortical tract in Friedreich ataxiaSirio Cocozza, Sara Bosticardo, Matteo Battocchio, et al.
Journal of Medical Genetics|September 21, 2021
A step forward, but still inadequate: Australian health professionals' views on the genetics and life insurance moratoriumJane M Tiller, Louise A Keogh, Aideen M McInerney-Leo, et al.
Neurology|July 11, 2022
Natural History of Friedreich Ataxia: Heterogeneity of Neurologic Progression and Consequences for Clinical Trial DesignChristian Rummey, Louise A Corben, Martin Delatycki, et al.
Journal of Medical Genetics|February 10, 2023
Population-based <i>BRCA1/2</i> testing programmes are highly acceptable in the Jewish community: results of the JeneScreen StudyJane M Tiller, Nicole E Cousens, Rajneesh Kaur, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
BMJ Open|June 3, 2023
Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocolSophie E Bouffler, Ling Lee, Fiona Lynch, et al.
Journal of Child Neurology|July 4, 2012
Friedreich ataxia clinical outcome measures: natural history evaluation in 410 participantsSean R Regner, Nicholas S Wilcox, Lisa S Friedman, et al.
Life Science Alliance|January 31, 2023
The ribose methylation enzyme FTSJ1 has a conserved role in neuron morphology and learning performanceMira Brazane, Dilyana G Dimitrova, Julien Pigeon, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Stem Cell Research|August 16, 2019
Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum DisorderKiymet Bozaoglu, Yujing Gao, Edouard Stanley, et al.
Brain : a Journal of Neurology|March 5, 2003
Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical courseFerdinando Squitieri, Cinzia Gellera, Milena Cannella, et al.
Annals of Clinical and Translational Neurology|July 2, 2024
Gradient of microstructural damage along the dentato-thalamo-cortical tract in Friedreich ataxiaSirio Cocozza, Sara Bosticardo, Matteo Battocchio, et al.
Journal of Medical Genetics|September 21, 2021
A step forward, but still inadequate: Australian health professionals' views on the genetics and life insurance moratoriumJane M Tiller, Louise A Keogh, Aideen M McInerney-Leo, et al.
Neurology|July 11, 2022
Natural History of Friedreich Ataxia: Heterogeneity of Neurologic Progression and Consequences for Clinical Trial DesignChristian Rummey, Louise A Corben, Martin Delatycki, et al.
Journal of Medical Genetics|February 10, 2023
Population-based <i>BRCA1/2</i> testing programmes are highly acceptable in the Jewish community: results of the JeneScreen StudyJane M Tiller, Nicole E Cousens, Rajneesh Kaur, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
BMJ Open|June 3, 2023
Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocolSophie E Bouffler, Ling Lee, Fiona Lynch, et al.
Journal of Child Neurology|July 4, 2012
Friedreich ataxia clinical outcome measures: natural history evaluation in 410 participantsSean R Regner, Nicholas S Wilcox, Lisa S Friedman, et al.
Life Science Alliance|January 31, 2023
The ribose methylation enzyme FTSJ1 has a conserved role in neuron morphology and learning performanceMira Brazane, Dilyana G Dimitrova, Julien Pigeon, et al.
Pageof 6