INSTITUTE OF BIOMEDICINE AND MOLECULAR GENETICS (IBGM)
Institute
Centre Hospitalier Regional et Universitaire de Lille
Lila, FranciaPublications in collaboration with researchers from 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