Improved anatomical reproducibility in quantitative lower‐limb muscle MRI

To compare the influence of two limb positions and slice prescription using scout‐image–based and surface‐anatomy–based methods on the reproducibility of quantitative MRI of lower‐limb muscles.

[1]  D. Felsenberg,et al.  Heterogeneous atrophy occurs within individual lower limb muscles during 60 days of bed rest. , 2012, Journal of applied physiology.

[2]  Susana Quijano-Roy,et al.  Whole body muscle MRI protocol: Pattern recognition in early onset NM disorders , 2012, Neuromuscular Disorders.

[3]  Volker Straub,et al.  Towards harmonization of protocols for MRI outcome measures in skeletal muscle studies: Consensus recommendations from two TREAT-NMD NMR workshops, 2 May 2010, Stockholm, Sweden, 1–2 October 2009, Paris, France , 2012, Neuromuscular Disorders.

[4]  Volker Straub,et al.  TREAT-NMD workshop: Pattern recognition in genetic muscle diseases using muscle MRI 25–26 February 2011, Rome, Italy , 2012, Neuromuscular Disorders.

[5]  T. Yousry,et al.  1700 MRI quantification of lower limb muscle fatty atrophy: a potential outcome measure in chronic neuromuscular diseases , 2012, Journal of Neurology Neurosurgery & Psychiatry.

[6]  R. Finkel,et al.  Thigh Muscle Volume Measured by Magnetic Resonance Imaging Is Stable Over a 6-Month Interval in Spinal Muscular Atrophy , 2011, Journal of Child Neurology.

[7]  K. Scheffler,et al.  Muscular involvement assessed by MRI correlates to motor function measurement values in oculopharyngeal muscular dystrophy , 2011, Journal of Neurology.

[8]  P. Bini,et al.  Changes in skeletal muscle qualities during enzyme replacement therapy in late-onset type II glycogenosis: temporal and spatial pattern of mass vs. strength response , 2010, Journal of Inherited Metabolic Disease.

[9]  G. Nicholson,et al.  Correlation between muscle atrophy on MRI and manual strength testing in hereditary neuropathies , 2010, Journal of Clinical Neuroscience.

[10]  M. Geschwind Are you Related to “the Geschwind?” , 2010, Neuropsychology Review.

[11]  M. Maas,et al.  Reliability of in vivo determination of forearm muscle volume using 3.0 T magnetic resonance imaging , 2010, Journal of magnetic resonance imaging : JMRI.

[12]  Zhaohua Ding,et al.  Repeatability of DTI‐based skeletal muscle fiber tracking , 2010, NMR in biomedicine.

[13]  X. Golay,et al.  P86 Inter-scan reproducibility of quantitative neuromuscular MRI , 2010, Neuromuscular Disorders.

[14]  M. Wattjes,et al.  Whole‐body high‐field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenita , 2010, Acta neurologica Scandinavica.

[15]  A. Pestronk,et al.  A phase I/IItrial of MYO‐029 in adult subjects with muscular dystrophy , 2008, Annals of neurology.

[16]  Brian C Clark,et al.  Reliability of techniques to assess human neuromuscular function in vivo. , 2007, Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology.

[17]  H. Schild,et al.  Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2 , 2006, Journal of Neurology.

[18]  D. Downham,et al.  Assessment of contractile and noncontractile components in human skeletal muscle by magnetic resonance imaging , 2002, Muscle & nerve.

[19]  D. Altman,et al.  STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT , 1986, The Lancet.

[20]  Klaus Bohndorf,et al.  Muscle cross-section measurement by magnetic resonance imaging , 2004, European Journal of Applied Physiology and Occupational Physiology.

[21]  H. Schild,et al.  Wattjes Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2 A whole body highfield MRI study , 2022 .