Universidad de Buenos Aires-ko ikertzaileekin lankidetzan egindako argitalpenak (4)

2023

  1. The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism

    Endocrine, Vol. 80, Núm. 1, pp. 47-53

2022

  1. Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis

    Endocrine, Vol. 77, Núm. 1, pp. 86-101

2018

  1. Is it all said for NSAIDs in alzheimer’s disease? Role of mitochondrial calcium uptake

    Current Alzheimer Research, Vol. 15, Núm. 6, pp. 504-510

  2. Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism

    Molecular and Cellular Endocrinology, Vol. 473, pp. 1-16