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Curr Neurovasc Res

M.HertzigM.SweeneyJ

Hereditary spastic paraplegia is a common phenotypic finding in ARG1 deficiency, P5CS deficiency and HHH syndrome: three inborn errors of metabolism caused by alteration of an interconnected pathway of glutamate and urea cycle metabolism

Number of Sessions: Total cost depends on the complete treatment plan, including maintenance doses

Por otro lado, es un nutriente asociado directamente con la prctica deportiva, ya que la L-Carnitina contribuye a mejorar la resistencia fsica, potenciando la generacin de energa durante los entrenamientos

rare but serious reactions include hypersensitivity