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Nadia Schoenmakers

Showing results (31-40 of 43) with videos related to

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The Journal of Clinical Investigation|March 19, 2010
Resistance to thyroid hormone is associated with raised energy expenditure, muscle mitochondrial uncoupling, and hyperphagiaCatherine S Mitchell, David B Savage, Sylvie Dufour, et al.
Thyroid : Official Journal of the American Thyroid Association|March 6, 2026
Finnish-Enriched SLC26A7 Variant in Congenital Hypothyroidism: Clinical Spectrum, Thyroid Histopathology, and Expression AnalysisLaura Niuro, Johanna Ojala, Rowmika Ravi, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2022
An Approach to a Patient With Primary Hyperparathyroidism and a Suspected Ectopic Parathyroid AdenomaClark Glasgow, Eunice Y C Lau, Luigi Aloj, et al.
European Journal of Endocrinology|October 17, 2025
EndoCompass project: research roadmap for thyroid endocrinologyAgnieszka Piekiełko-Witkowska, Rossella Elisei, Juliane Leger, et al.
The New England Journal of Medicine|December 16, 2011
A mutation in the thyroid hormone receptor alpha geneElena Bochukova, Nadia Schoenmakers, Maura Agostini, et al.
Hormone Research in Paediatrics|December 1, 2025
EndoCompass Project: Research Roadmap for Thyroid EndocrinologyAgnieszka Piekielko-Witkowska, Rossella Elisei, Juliane Léger, et al.
JCI Insight|October 19, 2018
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidismHakan Cangul, Xiao-Hui Liao, Erik Schoenmakers, et al.
The Journal of Clinical Endocrinology and Metabolism|October 26, 2019
IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory HyperfunctionSjoerd D Joustra, Ferdinand Roelfsema, A S Paul van Trotsenburg, et al.
The Journal of Clinical Endocrinology and Metabolism|August 16, 2016
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-SituAdeline K Nicholas, Eva G Serra, Hakan Cangul, et al.
Nature|April 14, 2026
Polyclonal selection of immune checkpoint mutations in thyroid autoimmunityPantelis A Nicola, Andrew R J Lawson, Alexandra Tidd, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
The Journal of Clinical Investigation|March 19, 2010
Resistance to thyroid hormone is associated with raised energy expenditure, muscle mitochondrial uncoupling, and hyperphagiaCatherine S Mitchell, David B Savage, Sylvie Dufour, et al.
Thyroid : Official Journal of the American Thyroid Association|March 6, 2026
Finnish-Enriched SLC26A7 Variant in Congenital Hypothyroidism: Clinical Spectrum, Thyroid Histopathology, and Expression AnalysisLaura Niuro, Johanna Ojala, Rowmika Ravi, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2022
An Approach to a Patient With Primary Hyperparathyroidism and a Suspected Ectopic Parathyroid AdenomaClark Glasgow, Eunice Y C Lau, Luigi Aloj, et al.
European Journal of Endocrinology|October 17, 2025
EndoCompass project: research roadmap for thyroid endocrinologyAgnieszka Piekiełko-Witkowska, Rossella Elisei, Juliane Leger, et al.
The New England Journal of Medicine|December 16, 2011
A mutation in the thyroid hormone receptor alpha geneElena Bochukova, Nadia Schoenmakers, Maura Agostini, et al.
Hormone Research in Paediatrics|December 1, 2025
EndoCompass Project: Research Roadmap for Thyroid EndocrinologyAgnieszka Piekielko-Witkowska, Rossella Elisei, Juliane Léger, et al.
JCI Insight|October 19, 2018
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidismHakan Cangul, Xiao-Hui Liao, Erik Schoenmakers, et al.
The Journal of Clinical Endocrinology and Metabolism|October 26, 2019
IGSF1 Deficiency Results in Human and Murine Somatotrope Neurosecretory HyperfunctionSjoerd D Joustra, Ferdinand Roelfsema, A S Paul van Trotsenburg, et al.
The Journal of Clinical Endocrinology and Metabolism|August 16, 2016
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-SituAdeline K Nicholas, Eva G Serra, Hakan Cangul, et al.
Nature|April 14, 2026
Polyclonal selection of immune checkpoint mutations in thyroid autoimmunityPantelis A Nicola, Andrew R J Lawson, Alexandra Tidd, et al.
Pageof 5