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39 TPI deficiency (OMIM 190450) is a relatively rare autosomal recessive multisystem disorder, characterized by hemolytic anemia, severe neuromuscular defects, increased susceptibility to infection, and cardiomyopathy.48,134,161 Patients usually die in childhood, although intriguing exceptions have been reported

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They then inhaled a nebulized solution containing 600 mg NAC 30 minutes prior to and after each subsequent radiation treatment

Med Sci Monit: Int Med J Expt Clin Res 23:2684 Xu Z et al (2021) Astragaloside IV protects 6-hydroxydopamine-induced SH-SY5Y cell model of Parkinsons disease via activating the JAK2/STAT3 pathway

Las modificaciones dietticas estratgicas pueden mitigar significativamente los problemas intestinales asociados con los medicamentos GLP-1, mejorando tanto la tolerabilidad como la efectividad del tratamiento