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C M Sue

Showing results (1-10 of 44) with videos related to

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Brain Pathology (Zurich, Switzerland)|July 8, 2000
Mitochondrial respiratory chain diseases and mutations in nuclear DNA: a promising start?C M Sue, E A Schon
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1997
Another case of Hashimoto's encephalopathyC M Sue, J G Morris
Neurology|February 11, 2000
Paroxysmal word deafness secondary to focal epilepsyV S Fung, C M Sue, E R Somerville
Journal of Neurology|July 22, 2015
A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian familyK E Ahmad, R L Davis, C M Sue
Internal Medicine Journal|December 21, 2012
SPAST mutations in Australian patients with hereditary spastic paraplegiaH Vandebona, N P Kerr, C Liang, et al.
Seminars in Perinatology|May 20, 1999
Neonatal presentations of mitochondrial metabolic disordersC M Sue, M Hirano, S DiMauro, et al.
The Medical Journal of Australia|May 15, 1995
Confusion, cortical blindness and feverC M Sue, J G Morris, J Leicester, et al.
Internal Medicine Journal|June 1, 2012
POLG mutations in Australian patients with mitochondrial diseaseP Woodbridge, C Liang, R L Davis, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 1, 1997
Transcranial cortical stimulation in disorders of the central motor pathwaysC M Sue, C Yiannikas, P D Clouston, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 1, 1997
Hashimoto's encephalopathyC M Sue, V Fung, J P Halpern, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Brain Pathology (Zurich, Switzerland)|July 8, 2000
Mitochondrial respiratory chain diseases and mutations in nuclear DNA: a promising start?C M Sue, E A Schon
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1997
Another case of Hashimoto's encephalopathyC M Sue, J G Morris
Neurology|February 11, 2000
Paroxysmal word deafness secondary to focal epilepsyV S Fung, C M Sue, E R Somerville
Journal of Neurology|July 22, 2015
A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian familyK E Ahmad, R L Davis, C M Sue
Internal Medicine Journal|December 21, 2012
SPAST mutations in Australian patients with hereditary spastic paraplegiaH Vandebona, N P Kerr, C Liang, et al.
Seminars in Perinatology|May 20, 1999
Neonatal presentations of mitochondrial metabolic disordersC M Sue, M Hirano, S DiMauro, et al.
The Medical Journal of Australia|May 15, 1995
Confusion, cortical blindness and feverC M Sue, J G Morris, J Leicester, et al.
Internal Medicine Journal|June 1, 2012
POLG mutations in Australian patients with mitochondrial diseaseP Woodbridge, C Liang, R L Davis, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 1, 1997
Transcranial cortical stimulation in disorders of the central motor pathwaysC M Sue, C Yiannikas, P D Clouston, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 1, 1997
Hashimoto's encephalopathyC M Sue, V Fung, J P Halpern, et al.
Pageof 5