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T Pulkes

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

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Advanced Drug Delivery Reviews|May 30, 2001
Human mitochondrial DNA diseasesT Pulkes, M G Hanna
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 31, 2010
CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in ThailandS Theerasasawat, C Papsing, T Pulkes
Lancet (London, England)|January 6, 2001
Increased risk of stroke in patients with the A12308G polymorphism in mitochondriaT Pulkes, M G Sweeney, M G Hanna
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|June 8, 2006
Levodopa induced motor complications in Thai Parkinson's disease patientsK Kulkantrakorn, S Tiamkao, C Pongchaiyakul, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 15, 2011
Mutation and haplotype analysis of oculopharyngeal muscular dystrophy in Thai patientsT Pulkes, C Papsing, M Busabaratana, et al.
Neurology|November 9, 2000
A novel mutation in the mitochondrial tRNA(TYr) gene associated with exercise intoleranceT Pulkes, A Siddiqui, J A Morgan-Hughes, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 26, 2011
Association between apolipoprotein E genotypes and Parkinson's diseaseT Pulkes, C Papsing, S Mahasirimongkol, et al.
Neurology|March 23, 2005
Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intoleranceT Pulkes, D Liolitsa, A J Wills, et al.
Neuromuscular Disorders : NMD|March 13, 2012
Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: CorrectionR Witoonpanich, T Pulkes, C Dejthevaporn, et al.
Annals of Neurology|December 10, 1999
The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAST Pulkes, L Eunson, V Patterson, et al.
Pageof 2

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

Sort By:
Pageof 2
Advanced Drug Delivery Reviews|May 30, 2001
Human mitochondrial DNA diseasesT Pulkes, M G Hanna
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 31, 2010
CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in ThailandS Theerasasawat, C Papsing, T Pulkes
Lancet (London, England)|January 6, 2001
Increased risk of stroke in patients with the A12308G polymorphism in mitochondriaT Pulkes, M G Sweeney, M G Hanna
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|June 8, 2006
Levodopa induced motor complications in Thai Parkinson's disease patientsK Kulkantrakorn, S Tiamkao, C Pongchaiyakul, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 15, 2011
Mutation and haplotype analysis of oculopharyngeal muscular dystrophy in Thai patientsT Pulkes, C Papsing, M Busabaratana, et al.
Neurology|November 9, 2000
A novel mutation in the mitochondrial tRNA(TYr) gene associated with exercise intoleranceT Pulkes, A Siddiqui, J A Morgan-Hughes, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 26, 2011
Association between apolipoprotein E genotypes and Parkinson's diseaseT Pulkes, C Papsing, S Mahasirimongkol, et al.
Neurology|March 23, 2005
Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intoleranceT Pulkes, D Liolitsa, A J Wills, et al.
Neuromuscular Disorders : NMD|March 13, 2012
Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: CorrectionR Witoonpanich, T Pulkes, C Dejthevaporn, et al.
Annals of Neurology|December 10, 1999
The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAST Pulkes, L Eunson, V Patterson, et al.
Pageof 2