Upper Motor Neuron Disorders: Primary Lateral Sclerosis, Upper Motor Neuron Dominant Amyotrophic Lateral Sclerosis, and Hereditary Spastic Paraplegia

Lignende værker

• Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions
  af: Denora, Paola S., et al.
  Udgivet: (2016)
• SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia
  af: Osmanovic, Alma, et al.
  Udgivet: (2020)
• Motor Neuron Firing Dysfunction in Spastic Patients With Primary Lateral Sclerosis
  af: Floeter, Mary Kay, et al.
  Udgivet: (2005)
• Dominant Heterogeneity of Upper and Lower Motor Neuron Degeneration to Motor Manifestation of Involved Region in Amyotrophic Lateral Sclerosis
  af: Jin, Jiaoting, et al.
  Udgivet: (2019)
• The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia
  af: Meyer, T., et al.
  Udgivet: (1998)