Yoshio Tsuboi

Yoshio Tsuboi

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Yoshio Tsuboi has a total of 6 co-authors. Here are the top co-authors by number of shared publications:

  • Hiroyasu Kawano

    Department of Pediatrics, Fukuoka University School of Medicine, Fukuoka, Japan

    1 shared publication
  • Jiro Fukae

    Department of Neurology, Fukuoka University School of Medicine, Fukuoka, Japan

    1 shared publication
  • Jun Tsugawa

    Stroke center, Fukuoka University Chikushi Hospital, Fukuoka, Japan

    1 shared publication
  • Ken-Ichi Inoue

    Department of Neurology, Fukuoka University School of Medicine, Fukuoka, Japan

    1 shared publication
  • Kosuke Fukuhara

    Department of Neurology, Fukuoka University School of Medicine, Fukuoka, Japan

    1 shared publication
  • Shinsuke Fujioka

    Department of Neurology, Fukuoka University School of Medicine, Fukuoka, Japan

    1 shared publication

Latest Publications

  • Open Access

    Myasthenia Gravis with Anti-Muscle-Specific Tyrosine Kinase Antibody during Pregnancy and Risk of Neonatal Myasthenia Gravis: A Case Report and Review of the Literature

    by Ken-Ichi Inoue, Jun Tsugawa, Jiro Fukae, Kosuke Fukuhara, Hiroyasu Kawano, Shinsuke Fujioka, Yoshio Tsuboi

    A 31-year-old woman presented with a nasal voice, dysarthria, and upper limb weakness during her first pregnancy. Soon after delivery of her first baby, her symptoms disappeared. At the age of 34 years, during her second pregnancy, her nasal voice re-appeared. After delivery of the second baby, her nasal voice worsened, and bilateral eyelid ptosis and easy fatigability were also evident. She was referred to our hospital. Because of her myasthenic symptoms and anti-muscle-specific tyrosine kinase (MuSK) antibody (Ab)-positive status, she was diagnosed as having myasthenia gravis (MG). Her symptoms were worse than those in her first pregnancy. She was treated with oral steroid and double filtration plasmapheresis. After initiation of treatment, her myasthenic symptoms improved completely. In addition, her baby developed transient neonatal MG (TNMG) on the fourth day after birth and then gradually recovered over 30 days. It should be noted that symptoms of patients with anti-MuSK Ab-positive MG (MuSK-MG) can deteriorate during pregnancy, and the babies delivered of patients with MuSK-MG have a high probability of developing TNMG.