1. Autosomal recessive axonal neuropathy caused by HINT1 mutation: new association of a psychiatric disorder to the neurologic phenotype

    http://dx.doi.org/10.1016/j.nmd.2019.05.001
  2. Newborn screening for SMA in Southern Belgium

    http://dx.doi.org/10.1016/j.nmd.2019.02.003
  3. ACTA1-myopathy with prominent finger flexor weakness and rimmed vacuoles

    http://dx.doi.org/10.1016/j.nmd.2019.02.012
  4. Wrist drop in an arcade dancing game: Unusual sudden bilateral radial palsy

    http://dx.doi.org/10.1016/j.nmd.2019.02.005
  5. Exome sequencing detects compound heterozygous nonsense LAMA2 mutations in two siblings with atypical phenotype and nearly normal brain MRI

    http://dx.doi.org/10.1016/j.nmd.2019.04.001
  6. Editorial Board

    http://dx.doi.org/10.1016/s0960-8966(19)30281-0
  7. Thoracic circumference: A new outcome measure in spinal muscular atrophy type 1?

    http://dx.doi.org/10.1016/j.nmd.2019.03.003
  8. Central drive and ventilatory failure in late-onset Pompe disease: At the gates of a new phenotype

    http://dx.doi.org/10.1016/j.nmd.2019.03.008
  9. Surgical outcomes of cavovarus foot deformity in children with Charcot-Marie-Tooth disease

    http://dx.doi.org/10.1016/j.nmd.2019.04.004
  10. 1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018

    http://dx.doi.org/10.1016/j.nmd.2019.03.002
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