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  1. Current status of non-invasive prenatal testing in Japan
  2. QOL in caregivers of Japanese patients with Prader–Willi syndrome with reference to age and genotype
  3. Autism spectrum disorders and hyperactive/impulsive behaviors in Japanese patients with Prader–Willi syndrome: A comparison between maternal uniparental disomy and deletion cases
  4. Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations
  5. Testosterone replacement therapy to improve secondary sexual characteristics and body composition without adverse behavioral problems in adult male patients with Prader–Willi syndrome: An observational study
  6. Scoliosis in Prader–Willi syndrome: Effect of growth hormone therapy and value of paravertebral muscle volume by CT in predicting scoliosis progression
  7. Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation