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P M Matthews

Showing results (161-170 of 182) with videos related to

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Neuromuscular Disorders : NMD|May 1, 1995
Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriersP M Matthews, D Benjamin, I Van Bakel, et al.
Magnetic Resonance in Medicine|October 31, 2003
Characterization and propagation of uncertainty in diffusion-weighted MR imagingT E J Behrens, M W Woolrich, M Jenkinson, et al.
Brain : a Journal of Neurology|June 1, 1994
Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patientsP M Matthews, R M Brown, L J Otero, et al.
Neuroimage|August 15, 2009
Longitudinal changes in grey and white matter during adolescenceA Giorgio, K E Watkins, M Chadwick, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 2, 2004
Changes in connectivity profiles define functionally distinct regions in human medial frontal cortexH Johansen-Berg, T E J Behrens, M D Robson, et al.
Annals of Neurology|July 1, 1994
Pyruvate dehydrogenase deficiency: molecular basis for intrafamilial heterogeneityT Fujii, R N Van Coster, S E Old, et al.
Neurology|April 12, 2003
Evidence of early cortical atrophy in MS: relevance to white matter changes and disabilityN De Stefano, P M Matthews, M Filippi, et al.
Neuroimage|August 14, 2010
Differential effects of the APOE genotype on brain function across the lifespanN Filippini, K P Ebmeier, B J MacIntosh, et al.
Neuroimage|February 14, 2006
Reliable identification of the auditory thalamus using multi-modal structural analysesJ T Devlin, E L Sillery, D A Hall, et al.
Osteoarthritis and Cartilage|November 2, 2011
Reproducibility of sodium MRI measures of articular cartilage of the knee in osteoarthritisR D Newbould, S R Miller, J A W Tielbeek, et al.
Pageof 19

Showing results (161-170 of 182) with videos related to

Sort By:
Pageof 19
Neuromuscular Disorders : NMD|May 1, 1995
Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriersP M Matthews, D Benjamin, I Van Bakel, et al.
Magnetic Resonance in Medicine|October 31, 2003
Characterization and propagation of uncertainty in diffusion-weighted MR imagingT E J Behrens, M W Woolrich, M Jenkinson, et al.
Brain : a Journal of Neurology|June 1, 1994
Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patientsP M Matthews, R M Brown, L J Otero, et al.
Neuroimage|August 15, 2009
Longitudinal changes in grey and white matter during adolescenceA Giorgio, K E Watkins, M Chadwick, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 2, 2004
Changes in connectivity profiles define functionally distinct regions in human medial frontal cortexH Johansen-Berg, T E J Behrens, M D Robson, et al.
Annals of Neurology|July 1, 1994
Pyruvate dehydrogenase deficiency: molecular basis for intrafamilial heterogeneityT Fujii, R N Van Coster, S E Old, et al.
Neurology|April 12, 2003
Evidence of early cortical atrophy in MS: relevance to white matter changes and disabilityN De Stefano, P M Matthews, M Filippi, et al.
Neuroimage|August 14, 2010
Differential effects of the APOE genotype on brain function across the lifespanN Filippini, K P Ebmeier, B J MacIntosh, et al.
Neuroimage|February 14, 2006
Reliable identification of the auditory thalamus using multi-modal structural analysesJ T Devlin, E L Sillery, D A Hall, et al.
Osteoarthritis and Cartilage|November 2, 2011
Reproducibility of sodium MRI measures of articular cartilage of the knee in osteoarthritisR D Newbould, S R Miller, J A W Tielbeek, et al.
Pageof 19