INSTITUTO DE BIOMEDICINA Y GENÉTICA MOLECULAR (IBGM)
Instituto
Centre Hospitalier Regional et Universitaire de Lille
Lila, FranciaPublicaciones en colaboración con investigadores/as de Centre Hospitalier Regional et Universitaire de Lille (6)
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
2021
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Global impact of COVID-19 on stroke care
International Journal of Stroke, Vol. 16, Núm. 5, pp. 573-584
2019
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Extending thrombolysis to 4·5–9 h and wake-up stroke using perfusion imaging: a systematic review and meta-analysis of individual patient data
The Lancet, Vol. 394, Núm. 10193, pp. 139-147
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