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C M Sue

Showing results (11-20 of 44) with videos related to

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Internal Medicine Journal|June 15, 2007
Population prevalence and incidence of Parkinson's disease in an Australian communityP Mehta, A Kifley, J J Wang, et al.
BMJ Case Reports|July 7, 2011
Mitochondrial disease mimicking Charcot-Marie Tooth diseaseM Needham, J Duley, S Hammond, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2006
Mitochondrial disease mimicking Charcot-Marie Tooth diseaseM Needham, J Duley, S Hammond, et al.
Internal Medicine Journal|July 27, 2006
Prevalence of mitochondrial DNA haplogroups in an Australian populationN Manwaring, M M Jones, J J Wang, et al.
Neurology|October 27, 1997
Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutationC M Sue, P Mitchell, D S Crimmins, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 23, 2008
Is Sydenham's chorea an antiphospholipid syndrome?V S Fung, C Yiannikas, C M Sue, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Measurement of ATP production in mitochondrial disordersR K Shepherd, N Checcarelli, A Naini, et al.
Journal of the Neurological Sciences|January 8, 1999
Detection of MELAS A3243G point mutation in muscle, blood and hair folliclesC M Sue, A Quigley, S Katsabanis, et al.
Lancet (London, England)|February 13, 1993
Mitochondrial gene mutations and diabetes mellitusC M Sue, D J Holmes-Walker, J G Morris, et al.
European Journal of Neurology|February 17, 2015
Cortical excitability changes distinguish the motor neuron disease phenotypes from hereditary spastic paraplegiaN Geevasinga, P Menon, C M Sue, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Internal Medicine Journal|June 15, 2007
Population prevalence and incidence of Parkinson's disease in an Australian communityP Mehta, A Kifley, J J Wang, et al.
BMJ Case Reports|July 7, 2011
Mitochondrial disease mimicking Charcot-Marie Tooth diseaseM Needham, J Duley, S Hammond, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2006
Mitochondrial disease mimicking Charcot-Marie Tooth diseaseM Needham, J Duley, S Hammond, et al.
Internal Medicine Journal|July 27, 2006
Prevalence of mitochondrial DNA haplogroups in an Australian populationN Manwaring, M M Jones, J J Wang, et al.
Neurology|October 27, 1997
Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutationC M Sue, P Mitchell, D S Crimmins, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 23, 2008
Is Sydenham's chorea an antiphospholipid syndrome?V S Fung, C Yiannikas, C M Sue, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Measurement of ATP production in mitochondrial disordersR K Shepherd, N Checcarelli, A Naini, et al.
Journal of the Neurological Sciences|January 8, 1999
Detection of MELAS A3243G point mutation in muscle, blood and hair folliclesC M Sue, A Quigley, S Katsabanis, et al.
Lancet (London, England)|February 13, 1993
Mitochondrial gene mutations and diabetes mellitusC M Sue, D J Holmes-Walker, J G Morris, et al.
European Journal of Neurology|February 17, 2015
Cortical excitability changes distinguish the motor neuron disease phenotypes from hereditary spastic paraplegiaN Geevasinga, P Menon, C M Sue, et al.
Pageof 5