Movement Disorder Perspectives on Monocarboxylate 8 Deficiency: A Case Series of 3 Colombian Patients with Allan–Herndon–Dudley Syndrome

Ähnliche Einträge

• Erratum to “Movement Disorder Perspectives at MCT8 Deficiency: A Case Series of Three Colombian Patients With Allan Herndon Dudley Syndrome”
  Veröffentlicht: (2025)
• Patients with Allan‐Herndon‐Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment
  von: Nina‐Maria Wilpert, et al.
  Veröffentlicht: (2025)
• GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and Anemia
  von: Sangeetha Yoganathan, et al.
  Veröffentlicht: (2026)
• Two Novel Movement Disorders with Osmotic Demyelination Syndrome
  von: Shreyashi Jha
  Veröffentlicht: (2025)
• Vitamin C Deficiency Presenting with Progressive Gait Difficulty, Myopathy, and Movement Disorder in a Toddler
  von: Vanessa Hwee Ling Ng, et al.
  Veröffentlicht: (2025)