INSTITUTO DE INVESTIGACIÓN BIOMÉDICA DE SALAMANCA
Instituto
Universidad de Buenos Aires
Buenos Aires, ArgentinaPublicaciones en colaboración con investigadores/as de Universidad de Buenos Aires (33)
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
2021
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A Global Survey on Changes in the Supply, Price, and Use of Illicit Drugs and Alcohol, and Related Complications During the 2020 COVID-19 Pandemic
Frontiers in Psychiatry, Vol. 12
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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Reorganization of Substance Use Treatment and Harm Reduction Services During the COVID-19 Pandemic: A Global Survey
Frontiers in Psychiatry, Vol. 12
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Ursodeoxycholic acid in intrahepatic cholestasis of pregnancy: A systematic review and individual participant data meta-analysis
Obstetrical and Gynecological Survey
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Ursodeoxycholic acid in intrahepatic cholestasis of pregnancy: a systematic review and individual participant data meta-analysis
The Lancet Gastroenterology and Hepatology, Vol. 6, Núm. 7, pp. 547-558
2019
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Association of adverse perinatal outcomes of intrahepatic cholestasis of pregnancy with biochemical markers: Results of aggregate and individual patient data meta-analyses
Obstetrical and Gynecological Survey
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Association of adverse perinatal outcomes of intrahepatic cholestasis of pregnancy with biochemical markers: results of aggregate and individual patient data meta-analyses
The Lancet, Vol. 393, Núm. 10174, pp. 899-909
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What is new in teaching science structured around the notion of 'scientific competence'?
CEUR Workshop Proceedings
2018
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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
2016
2015
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Kinetic characterization of human thyroperoxidase. Normal and pathological enzyme expression in Baculovirus System: A molecular model of functional expression
Molecular and Cellular Endocrinology, Vol. 404, pp. 9-15
2014
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QSAR on antiproliferative naphthoquinones based on a conformation- independent approach
European Journal of Medicinal Chemistry, Vol. 77, pp. 176-184
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UV irradiation accelerates amyloid precursor protein (APP) processing and disrupts APP axonal transport
Journal of Neuroscience, Vol. 34, Núm. 9, pp. 3320-3339
2012
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Congenital goitrous hypothyroidism: Mutation analysis in the thyroid peroxidase gene
Clinical Endocrinology, Vol. 76, Núm. 4, pp. 568-576
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Guidelines for the use and interpretation of assays for monitoring autophagy
Autophagy, Vol. 8, Núm. 4, pp. 445-544
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Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: Identification a cryptic donor splice site in the exon 19
Molecular and Cellular Endocrinology, Vol. 348, Núm. 1, pp. 313-321