Familial ALS With p. L127S ( L126S ) Variant of the Cu/Zn SOD1 Gene: A Report of Two New Cases and Literature Review

Documenti analoghi

• An Autopsy Case of ALS Which Clinically Presented Sporadic Adult‐Onset Lower Motor Neuron Disease and Genetically Had p. Leu127Ser ( L126S ) Variant in SOD1 and SMN2 Deletion
  di: Kimiko Inoue, et al.
  Pubblicazione: (2025)
• Computational Analysis of SOD1‐G93A Mouse Muscle Biomarkers for Comprehensive Assessment of ALS Progression
  di: Pedro Gómez‐Gálvez, et al.
  Pubblicazione: (2025)
• Perineuronal nets are phagocytosed by MMP‐9 expressing microglia and astrocytes in the SOD1 G93A ALS mouse model
  di: Sang Won Cheung, et al.
  Pubblicazione: (2024)
• An autopsy report of a long‐survival case of familial amyotrophic lateral sclerosis with SOD1 G93S gene mutation: Lack of SOD1‐positive inclusion in the remaining neurons
  di: Asuka Funai, et al.
  Pubblicazione: (2024)
• Pleiotrophin/Midkine Pathway Is Dysregulated in a TDP ‐ 43 A315T Mouse Model of Amyotrophic Lateral Sclerosis ( ALS )
  di: Paloma Martínez‐Alesón, et al.
  Pubblicazione: (2026)