Now showing items 1-2 of 2

    • Campanholi, Diana Ruffato Resende; Margutti, Ana Vitoria Barban; Silva, Wilson A.; Garcia, Daniel F.; Molfetta, Greice A.; Marques, Adriana A.; Schwartz, Ida Vanessa Döederlein; Cornejo Espinoza, Verónica del Carmen; Hamilton Viollier, Valerie; Castro Chávez, Gabriela; Sperb Ludwig, Fernanda; Borges, Ester S.; Camelo, José S (Wiley, 2021)
      Background Maple syrup urine disease (MSUD) is an autosomal recessive inherited metabolic disorder caused by the deficient activity of the branched-chain alpha-keto acid dehydrogenase (BCKD) enzymatic complex. BCKD is a ...
    • Fuenzalida, Karen; Leal Witt, María Jesús; Guerrero, Patricio; Hamilton Viollier, Valerie; Salazar, María Florencia; Peñaloza, Felipe; Arias Pefaur, Carolina; Cornejo Espinoza, Veronica del Carmen (MDPI, 2021)
      Treatment and follow-up in Hereditary Tyrosinemia type 1 (HT-1) patients require comprehensive clinical and dietary management, which involves drug therapy with NTBC and the laboratory monitoring of parameters, including ...