Visser, Theo J.

Rapid and selective inner ring deiodination of thyroxine sulfate by rat-liver deiodinase

MOL, J. A., & VISSER, T. J. (1985) · Endocrinology

Thyroid Disorders and TreatmentsPharmacogenetics and Drug Metabolism

Cited by 76

Disorder of thyroid hormone transport into the tissues

Groeneweg, S., Visser, W. E., & Visser, T. J. (2017) · Best Practice & Research Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsDrug Transport and Resistance Mechanisms

Cited by 75

Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations

Visser, W. E., Jansen, J., Friesema, E. C. H., Kester, M. H. A., Mancilla, E., Lundgren, J., van der Knaap, M. S., Lunsing, R. J., Brouwer, O. F., & Visser, T. J. (2009) · Human Mutation

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 75

Distribution of thyrotropin-releasing hormone (TRH)-containing cells and fibers in the human hypothalamus

Fliers, E., Noppen, N. W. A. M., Wiersinga, W. M., Visser, T. J., & Swaab, D. F. (1994) · Journal of Comparative Neurology

Hypothalamic control of reproductive hormonesNeuropeptides and Animal Physiology

Cited by 73

Type 3 Deiodinase Is Highly Expressed in Infiltrating Neutrophilic Granulocytes in Response to Acute Bacterial Infection

Boelen, A., Boorsma, J., Kwakkel, J., Wieland, C. W., Renckens, R., Visser, T. J., Fliers, E., & Wiersinga, W. M. (2008) · Thyroid

Thyroid Disorders and TreatmentsNeutrophil, Myeloperoxidase and Oxidative Mechanisms

Cited by 70

Different effects of continuous infusion of interleukin-1 and interleukin-6 on the hypothalamic-hypophysial-thyroid axis.

van Haasteren, G. A., van der Meer, M. J., Hermus, A. R., Linkels, E., Klootwijk, W., Kaptein, E., van Toor, H., Sweep, C. G., Visser, T. J., & de Greef, W. J. (1994) · Endocrinology

Thyroid Disorders and TreatmentsGrowth Hormone and Insulin-like Growth Factors

Cited by 69

Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations

Demir, K., van Gucht, A. L. M., Büyükinan, M., Çatlı, G., Ayhan, Y., Baş, V. N., Dündar, B., Özkan, B., Meima, M. E., Visser, W. E., et al. (2016) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 69

A large-scale association analysis of 68 thyroid hormone pathway genes with serum TSH and FT4 levels

Medici, M., van der Deure, W. M., Verbiest, M., Vermeulen, S. H., Hansen, P. S., Kiemeney, L. A., Hermus, A. R. M. M., Breteler, M. M., Hofman, A., Hegedüs, L., et al. (2011) · European Journal of Endocrinology

Thyroid Disorders and TreatmentsGenetic Associations and Epidemiology

Cited by 68

Resistance to Thyroid Hormone Alpha in an 18-Month-Old Girl: Clinical, Therapeutic, and Molecular Characteristics

van Gucht, A. L. M., Meima, M. E., Zwaveling-Soonawala, N., Visser, W. E., Fliers, E., Wennink, J. M. B., Henny, C., Visser, T. J., Peeters, R. P., & van Trotsenburg, A. S. P. (2016) · Thyroid

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 67

Pilot study on the assessment of the setpoint of the hypothalamus-pituitary-thyroid axis in healthy volunteers

Benhadi, N., Fliers, E., Visser, T. J., Reitsma, J. B., & Wiersinga, W. M. (2010) · European Journal of Endocrinology

Thyroid Disorders and TreatmentsClinical Laboratory Practices and Quality Control

Cited by 66

The pathophysiological consequences of thyroid hormone transporter deficiencies: Insights from mouse models

Heuer, H., & Visser, T. J. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects

Thyroid Disorders and TreatmentsDrug Transport and Resistance Mechanisms

Cited by 64

Concentrations of seven iodothyronine metabolites in brain regions and the liver of the adult rat

Pinna, G., Brödel, O., Visser, T., Jeitner, A., Grau, H., Eravci, M., Meinhold, H., & Baumgartner, A. (2002) · Endocrinology

Thyroid Disorders and TreatmentsGrowth Hormone and Insulin-like Growth Factors

Cited by 59

Bexarotene-induced hypothyroidism: Bexarotene stimulates the peripheral metabolism of thyroid hormones

Smit, J. W. A., Stokkel, M. P. M., Pereira, A. M., Romijn, J. A., & Visser, T. J. (2007) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsThyroid Cancer Diagnosis and Treatment

Cited by 59

Childhood Thyroid Function Reference Ranges and Determinants: A Literature Overview and a Prospective Cohort Study

Önsesveren, I., Barjaktarovic, M., Chaker, L., de Rijke, Y. B., Jaddoe, V. W. V., van Santen, H. M., Visser, T. J., Peeters, R. P., & Korevaar, T. I. M. (2017) · Thyroid®

Thyroid Disorders and TreatmentsClinical Laboratory Practices and Quality Control

Cited by 58

Increased Thyroxine Sulfate Levels in Critically Ill Patients as a Result of a Decreased Hepatic Type I Deiodinase Activity

Peeters, R. P., Kester, M. H. A., Wouters, P. J., Kaptein, E., van Toor, H., Visser, T. J., & Van den Berghe, G. (2005) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsAdrenal Hormones and Disorders

Cited by 57

Transport of Iodothyronines by Human L-Type Amino Acid Transporters

Zevenbergen, C., Meima, M. E., Lima de Souza, E. C., Peeters, R. P., Kinne, A., Krause, G., Visser, W. E., & Visser, T. J. (2015) · Endocrinology

Amino Acid Enzymes and MetabolismThyroid Disorders and Treatments

Cited by 55

Thr92Ala polymorphism in the type 2 deiodinase is not associated with T4 dose in athyroid patients or patients with Hashimoto thyroiditis

Heemstra, K. A., Hoftijzer, H. C., Van Der Deure, W. M., Peeters, R. P., Fliers, E., Appelhof, B. C., Wiersinga, W. M., Corssmit, E. P. M., Visser, T. J., & Smit, J. W. A. (2009) · Clinical Endocrinology

Thyroid Disorders and TreatmentsThyroid Cancer Diagnosis and Treatment

Cited by 51

Fatigue and fatigue-related symptoms in patients treated for different causes of hypothyroidism

Louwerens, M., Appelhof, B. C., Verloop, H., Medici, M., Peeters, R. P., Visser, T. J., Boelen, A., Fliers, E., Smit, J. W. A., & Dekkers, O. M. (2012) · European Journal of Endocrinology

Thyroid Disorders and TreatmentsThyroid Cancer Diagnosis and Treatment

Cited by 50

Mutations in MCT8 in patients with Allan-Herndon-Dudley-syndrome affecting its cellular distribution

Kersseboom, S., Kremers, G.-J., Friesema, E. C. H., Visser, W. E., Klootwijk, W., Peeters, R. P., & Visser, T. J. (2013) · Molecular Endocrinology

Thyroid Disorders and TreatmentsDrug Transport and Resistance Mechanisms

Cited by 45

Tissue mRNA expression of the glucocorticoid receptor and its splice variants in fatal critical illness

Peeters, R. P., Hagendorf, A., Vanhorebeek, I., Visser, T. J., Klootwijk, W., Mesotten, D., Wouters, P. J., Koper, J. W., De Jong, F. H., Feelders, R. A., et al. (2009) · Clinical Endocrinology

Adrenal Hormones and DisordersHyperglycemia and glycemic control in critically ill and hospitalized patients

Cited by 36

Relevance of Different Cellular Models in Determining the Effects of Mutations on SLC16A2/MCT8 Thyroid Hormone Transporter Function and Genotype-Phenotype Correlation

Capri, Y., Friesema, E. C. H., Kersseboom, S., Touraine, R., Monnier, A., Eymard-Pierre, E., Des Portes, V., De Michele, G., Brady, A. F., Boespflug-Tanguy, O., et al. (2013) · Human Mutation

Genomics and Rare DiseasesThyroid Disorders and Treatments

Cited by 33

Consumptive hypothyroidism: a case report and review of the literature

Jassam, N., Visser, T. J., Brisco, T., Bathia, D., McClean, P., & Barth, J. H. (2011) · Annals of Clinical Biochemistry International Journal of Laboratory Medicine

Thyroid Disorders and TreatmentsVascular Malformations and Hemangiomas

Cited by 32

Studies on the role of TRH and corticosterone in the regulation of prolactin and thyrotrophin secretion during lactation

van Haasteren, G. A. C., van Toor, H., Klootwijk, W., Handler, B., Linkels, E., van der Schoot, P., van Ophemert, J., de Jong, F. H., Visser, T. J., & de Greef, W. J. (1996) · Journal of Endocrinology

Growth Hormone and Insulin-like Growth FactorsHypothalamic control of reproductive hormones

Cited by 30

Transcriptional profiling of fibroblasts from patients with mutations in MCT8 and comparative analysis with the human brain transcriptome

Visser, W. E., Swagemakers, S. M. A., Őzgűr, Z., Schot, R., Verheijen, F. W., van Ijcken, W. F. J., van der Spek, P. J., & Visser, T. J. (2010) · Human Molecular Genetics

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 24