Bioquímica y Biología Molecular y Fisiología
Departamento
Universidad de Buenos Aires
Buenos Aires, ArgentinaPublicaciones en colaboración con investigadores/as de Universidad de Buenos Aires (4)
2023
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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
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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
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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
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Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism
Molecular and Cellular Endocrinology, Vol. 473, pp. 1-16