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D Hilton-Jones

Showing results (31-40 of 58) with videos related to

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Neuromuscular Disorders : NMD|March 21, 2001
Cardiac abnormalities and skeletal muscle weakness in carriers of Duchenne and Becker muscular dystrophies and controlsL Grain, M Cortina-Borja, C Forfar, et al.
European Journal of Neurology|April 21, 2010
EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemiaT Kyriakides, C Angelini, J Schaefer, et al.
Journal of Medical Genetics|January 1, 1994
Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissuesP M Matthews, J Hopkin, R M Brown, et al.
Journal of the Neurological Sciences|November 1, 1985
A mitochondrial encephalomyopathy. A combined 31P magnetic resonance and biochemical investigationD J Hayes, D Hilton-Jones, D L Arnold, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2002
An expanded cortical representation for hand movement after peripheral motor denervationH Reddy, D Bendahan, M A Lee, et al.
Lancet (London, England)|July 5, 1986
Biochemical investigation of human tumours in vivo with phosphorus-31 magnetic resonance spectroscopyR D Oberhaensli, D Hilton-Jones, P J Bore, et al.
Neuromuscular Disorders : NMD|March 20, 2012
Modafinil for excessive daytime sleepiness in myotonic dystrophy type 1--the patients' perspectiveD Hilton-Jones, M Bowler, H Lochmueller, et al.
Journal of the American College of Cardiology|November 25, 2000
Magnetic resonance spectroscopy evidence of abnormal cardiac energetics in Xp21 muscular dystrophyJ G Crilley, E A Boehm, B Rajagopalan, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Recurrent congenital arthrogryposis leading to a diagnosis of myasthenia gravis in an initially asymptomatic motherP R Barnes, D J Kanabar, L Brueton, et al.
Brain : a Journal of Neurology|November 25, 1998
Normal in vivo skeletal muscle oxidative metabolism in sporadic inclusion body myositis assessed by 31P-magnetic resonance spectroscopyR Lodi, D J Taylor, S J Tabrizi, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Neuromuscular Disorders : NMD|March 21, 2001
Cardiac abnormalities and skeletal muscle weakness in carriers of Duchenne and Becker muscular dystrophies and controlsL Grain, M Cortina-Borja, C Forfar, et al.
European Journal of Neurology|April 21, 2010
EFNS guidelines on the diagnostic approach to pauci- or asymptomatic hyperCKemiaT Kyriakides, C Angelini, J Schaefer, et al.
Journal of Medical Genetics|January 1, 1994
Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissuesP M Matthews, J Hopkin, R M Brown, et al.
Journal of the Neurological Sciences|November 1, 1985
A mitochondrial encephalomyopathy. A combined 31P magnetic resonance and biochemical investigationD J Hayes, D Hilton-Jones, D L Arnold, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2002
An expanded cortical representation for hand movement after peripheral motor denervationH Reddy, D Bendahan, M A Lee, et al.
Lancet (London, England)|July 5, 1986
Biochemical investigation of human tumours in vivo with phosphorus-31 magnetic resonance spectroscopyR D Oberhaensli, D Hilton-Jones, P J Bore, et al.
Neuromuscular Disorders : NMD|March 20, 2012
Modafinil for excessive daytime sleepiness in myotonic dystrophy type 1--the patients' perspectiveD Hilton-Jones, M Bowler, H Lochmueller, et al.
Journal of the American College of Cardiology|November 25, 2000
Magnetic resonance spectroscopy evidence of abnormal cardiac energetics in Xp21 muscular dystrophyJ G Crilley, E A Boehm, B Rajagopalan, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Recurrent congenital arthrogryposis leading to a diagnosis of myasthenia gravis in an initially asymptomatic motherP R Barnes, D J Kanabar, L Brueton, et al.
Brain : a Journal of Neurology|November 25, 1998
Normal in vivo skeletal muscle oxidative metabolism in sporadic inclusion body myositis assessed by 31P-magnetic resonance spectroscopyR Lodi, D J Taylor, S J Tabrizi, et al.
Pageof 6