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Jack W Miller

Showing results (1-10 of 11) with videos related to

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Primary Care|August 2, 2007
Screening children for developmental behavioral problems: principles for the practitionerJack W Miller
Neurobiology of Aging|July 14, 2012
Mutation analysis of VCP in British familial and sporadic amyotrophic lateral sclerosis patientsJack W Miller, Bradley N Smith, Simon D Topp, et al.
Neurobiology of Aging|August 16, 2012
Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patientsLauren Johnson, Jack W Miller, Athina Soragia Gkazi, et al.
Neurobiology of Aging|October 24, 2018
Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementiaSoragia Athina Gkazi, Claire Troakes, Simon Topp, et al.
Neurobiology of Aging|September 8, 2015
The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patientsChun Hao Wong, Simon Topp, Athina Soragia Gkazi, et al.
Brain : a Journal of Neurology|May 19, 2015
De novo point mutations in patients diagnosed with ataxic cerebral palsyRicardo Parolin Schnekenberg, Emma M Perkins, Jack W Miller, et al.
Cell Reports|December 3, 2013
Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxicYoun-Bok Lee, Han-Jou Chen, João N Peres, et al.
Science Translational Medicine|May 5, 2017
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosisBradley N Smith, Simon D Topp, Claudia Fallini, et al.
Neurobiology of Aging|September 11, 2012
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1Kreshnik B Ahmeti, Senda Ajroud-Driss, Ammar Al-Chalabi, et al.
Neuron|November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALSBradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Primary Care|August 2, 2007
Screening children for developmental behavioral problems: principles for the practitionerJack W Miller
Neurobiology of Aging|July 14, 2012
Mutation analysis of VCP in British familial and sporadic amyotrophic lateral sclerosis patientsJack W Miller, Bradley N Smith, Simon D Topp, et al.
Neurobiology of Aging|August 16, 2012
Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patientsLauren Johnson, Jack W Miller, Athina Soragia Gkazi, et al.
Neurobiology of Aging|October 24, 2018
Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementiaSoragia Athina Gkazi, Claire Troakes, Simon Topp, et al.
Neurobiology of Aging|September 8, 2015
The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patientsChun Hao Wong, Simon Topp, Athina Soragia Gkazi, et al.
Brain : a Journal of Neurology|May 19, 2015
De novo point mutations in patients diagnosed with ataxic cerebral palsyRicardo Parolin Schnekenberg, Emma M Perkins, Jack W Miller, et al.
Cell Reports|December 3, 2013
Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxicYoun-Bok Lee, Han-Jou Chen, João N Peres, et al.
Science Translational Medicine|May 5, 2017
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosisBradley N Smith, Simon D Topp, Claudia Fallini, et al.
Neurobiology of Aging|September 11, 2012
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1Kreshnik B Ahmeti, Senda Ajroud-Driss, Ammar Al-Chalabi, et al.
Neuron|November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALSBradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Pageof 2