J. de Vijlder

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The binding of NAD + and NADH to glyceraldehydephosphate dehydrogenase.

E. C. Slater, W. Boers, J. de Vijlder, 1970, Vitamins and hormones.

Function and role of NAD+ in mechanism of action of rabbit-muscle glyceraldehydephosphate dehydrogenase.

E. C. Slater, A. G. Hilvers, J. de Vijlder, 1969, Biochimica et biophysica acta.

Binding and properties of NAD+ in glyceraldehydephosphate dehydrogenase from lobster-tail muscle.

E. C. Slater, W. Boers, J. de Vijlder, 1969, Biochimica et biophysica acta.

The reaction of glyceraldehydephosphate dehydrogenase with NAD+.

E. C. Slater, J. de Vijlder, 1967, Biochimica et biophysica acta.

No damaging effect of chemotherapy in addition to radiotherapy on the thyroid axis in young adult survivors of childhood cancer.

M. Dijkgraaf, M. Jaspers, M. Offringa, 2003, The Journal of clinical endocrinology and metabolism.

Effects of pre- and postnatal exposure to chlorinated dioxins and furans on human neonatal thyroid hormone concentrations.

K. Olie, J. Koppe, J. de Vijlder, 1993, Environmental health perspectives.

Protection of the maternal and fetal thyroid from radioactive contamination by the administration of stable iodide during pregnancy. An experimental evaluation in chimpanzees.

J. J. Broerse, J. Broerse, J. de Vijlder, 1997, Radiation research.

Role of thallium-201 total-body scintigraphy in follow-up of thyroid carcinoma.

C. Hoefnagel, J. de Vijlder, C. Delprat, 1986, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

High incidence of thyroid dysfunction despite prophylaxis with potassium iodide during 131I‐meta‐iodobenzylguanidine treatment in children with neuroblastoma

H. V. van Santen, J. de Vijlder, B. V. van Eck, 2002, Cancer.

Identification of five novel inactivating mutations in the human thyroid peroxidase gene by denaturing gradient gel electrophoresis

F. Baas, J. de Vijlder, T. Vulsma, 1995, Human mutation.

Low maternal free thyroxine concentrations during early pregnancy are associated with impaired psychomotor development in infancy

W. Wiersinga, V. Pop, H. Drexhage, 1999, Clinical endocrinology.

Central congenital hypothyroidism due to gestational hyperthyroidism: detection where prevention failed.

M. Kempers, A. V. van Trotsenburg, J. de Vijlder, 2003, The Journal of clinical endocrinology and metabolism.

Lower neonatal screening thyroxine concentrations in down syndrome newborns.

H. V. van Santen, A. V. van Trotsenburg, J. de Vijlder, 2003, The Journal of clinical endocrinology and metabolism.

Maternal-fetal transfer of thyroxine in congenital hypothyroidism due to a total organification defect or thyroid agenesis.

J. de Vijlder, T. Vulsma, M. Gons, 1990, The New England journal of medicine.

Plasma thyrotropin bioactivity in Down's syndrome children with subclinical hypothyroidism.

C. Ris-Stalpers, J. de Vijlder, T. Vulsma, 2001, European journal of endocrinology.

Free thyroxine levels during the first weeks of life and neurodevelopmental outcome until the age of 5 years in very preterm infants.

A. V. van Baar, J. Kok, A. van Wassenaer, 2002, Pediatrics.

Hereditary congenital goiter with thyroglobulin deficiency in a breed of goats.

J. de Vijlder, A. Rijnberk, J. V. van Dijk, 1978, Endocrinology.

The Journal of Clinical Endocrinology & Metabolism Printed in U.S.A. Copyright © 2000 by The Endocrine Society Two Decades of Screening for Congenital Hypothyroidism in the Netherlands: TPO Gene Mutations in Total Iodide Organification Defects (an Update)

B. Bakker, J. D. Vijlder, J. de Vijlder, 2022 .

Two frequent missense mutations in Pendred syndrome.

E. Green, C. Cremers, N. Dietrich, 1998, Human molecular genetics.

Serum thyroglobulin and urinary iodine concentration are the most appropriate indicators of iodine status and thyroid function under conditions of increasing iodine supply in schoolchildren in Benin.

J. Hautvast, C. West, J. de Vijlder, 2001, The Journal of nutrition.

Absence of activating mutations in ras and gsp oncogenes in a cohort of nine patients with sporadic pediatric thyroid tumors.

C. Ris-Stalpers, J. D. Vijlder, J. de Vijlder, 2001, Medical and pediatric oncology.

Endocrine intervention during irradiation does not prevent damage to the thyroid gland.

J. Haveman, E. Endert, H. Rodermond, 2006, Thyroid : official journal of the American Thyroid Association.

Improved radiation protection of the thyroid gland with thyroxine, methimazole, and potassium iodide during diagnostic and therapeutic use of radiolabeled metaiodobenzylguanidine in children with neuroblastoma

H. V. van Santen, J. de Vijlder, B. V. van Eck, 2003, Cancer.

Serial analysis of gene expression as a tool to assess the human thyroid expression profile and to identify novel thyroidal genes.

F. Baas, C. Ris-Stalpers, M. Tijssen, 2000, The Journal of clinical endocrinology and metabolism.

Antithrombin Acts as a Negative Acute Phase Protein as Established with Studies on HepG2 Cells and in Baboons

R. W. Niessen, J. T. ten Cate, C. Hack, 1997, Thrombosis and Haemostasis.

Congenital hypothyroidism caused by a premature termination signal in exon 10 of the human thyroid peroxidase gene.

B. Bravenboer, J. de Vijlder, H. Bikker, 1996, The Journal of clinical endocrinology and metabolism.

A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect

M. Tambascia, G. Medeiros-Neto, J. de Vijlder, 1999, Clinical endocrinology.

A premature stopcodon in thyroglobulin messenger RNA results in familial goiter and moderate hypothyroidism.

C. Ris-Stalpers, M. Cammenga, H. Targovnik, 1999, The Journal of clinical endocrinology and metabolism.

Structure, function, and relevance of thyroid peroxidase in inherited diseases of the thyroid

C. Ris-Stalpers, J. de Vijlder, T. Vulsma, 1997 .

Human thyroglobulin reference material (CRM 457). 1st Part: Assessment of homogeneity, stability and immunoreactivity.

M. Schlumberger, G. Palumbo, D. Koutras, 1996, Annales de biologie clinique.

Up to date with human thyroglobulin.

C. Ris-Stalpers, H. Targovnik, J. de Vijlder, 2001, The Journal of endocrinology.

A premature stopcodon in thyroglobulin messenger RNA results in familial goiter and moderate hypothyroidism.

C. Ris-Stalpers, M. Cammenga, H. Targovnik, 1999, The Journal of clinical endocrinology and metabolism.

Studies on the structures of the normal and abnormal goat thyroglobulin genes.

F. Baas, G. van Ommen, J. de Vijlder, 1989, Biochimie.

Early assessment of hypothalamic-pituitary-gonadal function in patients with congenital hypothyroidism of central origin.

H. Delemarre-van de Waal, J. de Vijlder, T. Vulsma, 2007, The Journal of clinical endocrinology and metabolism.

The screening for mutations in the thyroglobulin cDNA from six patients with congenital hypothyroidism.

C. Ris-Stalpers, M. Cammenga, J. Orgiazzi, 1999, Biochimie.

The revised 8307 base pair coding sequence of human thyroglobulin transiently expressed in eukaryotic cells.

C. Ris-Stalpers, J. de Vijlder, E. Pauws, 1997, European journal of endocrinology.

Oculocutaneous albinism and skin cancer risk

H. C. de Vijlder, J. de Vijlder, H. Neumann, 2013, Journal of the European Academy of Dermatology and Venereology : JEADV.

Protection of the infant thyroid from radioactive contamination by the administration of stable iodide. An experimental evaluation in chimpanzees.

J. Broerse, J. de Vijlder, T. Vulsma, 1997, Radiation research.

Maternal-fetal transfer of thyroxine in congenital hypothyroidism due to a total organification defect or thyroid agenesis.

J. D. Vijlder, J. de Vijlder, T. Vulsma, 1989, The New England journal of medicine.

Disseminated medullary thyroid carcinoma despite early thyroid surgery in the multiple endocrine neoplasia-2A syndrome.

H. V. van Santen, A. V. van Trotsenburg, J. de Vijlder, 2005, Thyroid : official journal of the American Thyroid Association.

Maternal isodisomy for chromosome 2p causing severe congenital hypothyroidism.

R. Hennekam, R. Hennekam, B. Bakker, 2001, The Journal of clinical endocrinology and metabolism.

Primary congenital hypothyroidism: defects in iodine pathways.

J. de Vijlder, 2003, European journal of endocrinology.

Role of corticotropin-releasing hormone testing in assessment of hypothalamic-pituitary-adrenal axis function in infants with congenital central hypothyroidism.

J. de Vijlder, T. Vulsma, D. A. van Tijn, 2008, The Journal of clinical endocrinology and metabolism.

Thyroid function in very preterm newborns: possible implications.

J. Kok, A. van Wassenaer, J. D. Vijlder, 1999, Thyroid : official journal of the American Thyroid Association.

Morphological abnormalities in children with thyroidal congenital hypothyroidism

R. Hennekam, M. Kempers, K. Zwinderman, 2009, American journal of medical genetics. Part A.

Loss of integrity of thyroid morphology and function in children born to mothers with inadequately treated Graves' disease.

M. Kempers, R. V. van Rijn, A. V. van Trotsenburg, 2007, The Journal of clinical endocrinology and metabolism.

Neonatal screening for congenital hypothyroidism in the Netherlands: cognitive and motor outcome at 10 years of age.

M. Kempers, L. Kooistra, R. Nijhuis-van der Sanden, 2007, The Journal of clinical endocrinology and metabolism.

Normal ranges of T4 screening values in low birthweight infants.

E. Endert, J. Koppe, J. de Vijlder, 1983, Archives of disease in childhood.

Molecular basis of the thyroglobulin synthesis defect in Dutch goats.

J. de Vijlder, G. Veenboer, 1993, Endocrinology.

Effects of maternal thyroid status on thyroid hormones and growth in congenitally hypothyroid goat fetuses during the second half of gestation.

F. Baas, J. de Vijlder, J. van Doorn, 1997, Endocrinology.

Effects of Maternal Thyroid Status on Thyroid Hormones and Growth in Congenitally Hypothyroid Goat Fetuses during the Second Half of Gestation1.

F. Baas, J. D. Vijlder, J. de Vijlder, 1997, Endocrinology.

Circulating thyroglobulin measurements by homologous radioimmunoassay in dogs with thyroid carcinoma.

J. de Vijlder, J. Mol, P. Selman, 1991, Acta endocrinologica.

Characterization of and radioimmunoassay for canine thyroglobulin.

J. de Vijlder, J. Mol, P. Selman, 1991, Domestic animal endocrinology.

Concentration of plasma thyroglobulin and urinary excretion of iodinated material in the diagnosis of thyroid disorders in congenital hypothyroidism.

J. de Vijlder, J. Kok, M. Gons, 1983, Acta endocrinologica.

Autosomal recessive inheritance of goiter in Dutch goats.

F. Baas, G. van Ommen, J. de Vijlder, 1987, The Journal of heredity.

Congenital defect in iodothyronine synthesis. Clinical aspects of iodine metabolism in goats with congenital goitre and hypothyroidism.

J. de Vijlder, A. Rijnberk, J. V. van Dijk, 1977, The British veterinary journal.

Studies on the mechanism of inhibition of nuclear triiodothyronine binding by fatty acids

W. Wiersinga, J. de Vijlder, F. V. D. van der Klis, 1989, FEBS letters.

Dynamics of the plasma concentrations of TSH, FT4 and T3 following thyroxine supplementation in congenital hypothyroidism

M. Kempers, B. Bakker, J. de Vijlder, 2002, Clinical endocrinology.

Type II and type III deiodinase activity in human placenta as a function of gestational age.

T. Visser, C. Ris-Stalpers, J. de Vijlder, 1996, The Journal of clinical endocrinology and metabolism.

The human calbindin 27-kDa gene: structural organization of the 5' and 3' regions, chromosomal assignment, and restriction fragment length polymorphism.

M. Parmentier, G. Vassart, D. Lawson, 1989, Genomics.

Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism.

F. Baas, M. Kempers, C. Ris-Stalpers, 2002, The New England journal of medicine.

Regional localization of the gene for thyroid peroxidase to human chromosome 2pter----p12.

G. Vassart, F. Libert, J. de Vijlder, 1988, Cytogenetics and cell genetics.

Thyrotropin dependent and independent thyroid cell lines selected from FRTL-5 derived tumors grown in nude mice.

J. van den Brink, E. Schuuring, T. D. de Bruin, 1990, Endocrinology.

Correlation between the loss of thyroglobulin iodination and the expression of thyroid-specific proteins involved in iodine metabolism in thyroid carcinomas.

F. Miot, B. Franc, S. Costagliola, 2003, The Journal of clinical endocrinology and metabolism.

The effect of thyroxine treatment started in the neonatal period on development and growth of two-year-old Down syndrome children: a randomized clinical trial.

J. Tijssen, H. Heymans, A. V. van Baar, 2005, The Journal of clinical endocrinology and metabolism.

Euthyroidism via iodide supplementation in hereditary congenital goiter with thyroglobulin deficiency.

J. de Vijlder, J. V. van Dijk, W. F. van Voorthuizen, 1978, Endocrinology.

Trisomy 21 causes persistent congenital hypothyroidism presumably of thyroidal origin.

J. Tijssen, M. Kempers, E. Endert, 2006, Thyroid : official journal of the American Thyroid Association.

Comorbidity, Hospitalization, and Medication Use and Their Influence on Mental and Motor Development of Young Infants With Down Syndrome

J. Tijssen, H. Heymans, A. V. van Trotsenburg, 2006, Pediatrics.

Median Nerve Conduction Velocity and Central Conduction Time Measured With Somatosensory Evoked Potentials in Thyroxine-Treated Infants With Down Syndrome

J. Tijssen, A. V. van Trotsenburg, J. de Vijlder, 2006, Pediatrics.

Quantification of type III iodothyronine deiodinase activity using thin-layer chromatography and phosphor screen autoradiography.

T. Visser, J. de Vijlder, C. Schoenmakers, 1993, Analytical biochemistry.

Monoclonal antibodies to human thyroglobulin as probes for thyroglobulin structure.

M. D. de Baets, J. de Vijlder, P. J. Van Breda Vriesman, 1987, Endocrinology.

Effects of thyroxine supplementation on neurologic development in infants born at less than 30 weeks' gestation.

F. Dekker, A. V. van Baar, J. Kok, 1997, The New England journal of medicine.

Neonatal screening for congenital hypothyroidism based on thyroxine, thyrotropin, and thyroxine-binding globulin measurement: potentials and pitfalls.

M. Kempers, A. V. van Trotsenburg, J. de Vijlder, 2006, The Journal of clinical endocrinology and metabolism.

The quantity of thyroid hormone in human milk is too low to influence plasma thyroid hormone levels in the very preterm infant

F. Valianpour, A. van Wassenaer, P. Tamminga, 2002, Clinical endocrinology.

Neonatal Thyroxine Supplementation in Very Preterm Children: Developmental Outcome Evaluated at Early School Age

F. Dekker, A. V. van Baar, J. Kok, 2001, Pediatrics.

Changes in plasma thyroid hormone levels after a single dose of triiodothyronine in premature infants of less than 30 weeks gestational age.

F. Cools, J. Kok, A. van Wassenaer, 2000, European journal of endocrinology.

Thyroxine administration to infants of less than 30 weeks gestational age decreases plasma tri-iodothyronine concentrations.

F. Dekker, E. Endert, J. Kok, 1993, European journal of endocrinology.

Neonatal detection of congenital hypothyroidism of central origin.

J. de Vijlder, T. Vulsma, P. Verkerk, 2005, The Journal of clinical endocrinology and metabolism.

Intellectual and motor development of young adults with congenital hypothyroidism diagnosed by neonatal screening.

M. Kempers, L. Kooistra, M. Grootenhuis, 2006, The Journal of clinical endocrinology and metabolism.

Inborn errors of thyroid hormone biosynthesis.

C. Ris-Stalpers, J. de Vijlder, T. Vulsma, 1997, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Maternal hypothyroxinaemia during early pregnancy and subsequent child development: a 3‐year follow‐up study

V. Pop, A. V. van Baar, E. Brouwers, 2003, Clinical endocrinology.

Automated high-performance liquid chromatographic method for the determination of iodotyrosines and iodothyronines.

J. de Vijlder, E. Hogendoorn, C. E. Goewie, 1988, Journal of chromatography.

Molecular analysis of mutated thyroid peroxidase detected in patients with total iodide organification defects.

F. Baas, J. de Vijlder, H. Bikker, 1997, The Journal of clinical endocrinology and metabolism.

Use of amiodarone during pregnancy.

J. de Vijlder, T. A. Plomp, T. Vulsma, 1992, European journal of obstetrics, gynecology, and reproductive biology.

Thyroid albumin originates from blood.

J. de Vijlder, J. V. van Dijk, G. Veenboer, 1992, Endocrinology.

Heterogeneity in polyadenylation cleavage sites in mammalian mRNA sequences: implications for SAGE analysis.

E Pauws, A. V. van Kampen, C. Ris-Stalpers, 2001, Nucleic acids research.

The human thyroglobulin gene contains two 15-17 kb introns near its 3'-end.

F. Baas, A. Arnberg, G. van Ommen, 1983, Nucleic acids research.

Role of the thyrotropin-releasing hormone stimulation test in diagnosis of congenital central hypothyroidism in infants.

J. de Vijlder, T. Vulsma, D. A. van Tijn, 2008, The Journal of clinical endocrinology and metabolism.

Clinical Effectiveness and Cost-Effectiveness of the Use of the Thyroxine/Thyroxine-Binding Globulin Ratio to Detect Congenital Hypothyroidism of Thyroidal and Central Origin in a Neonatal Screening Program

J. Loeber, J. de Vijlder, T. Vulsma, 2005, Pediatrics.

Freeze fracture morphology of thyroid tight junctions in goats with different thyrotropin stimulation.

J. de Vijlder, J. V. van Dijk, C. Koch, 1985, Endocrinology.

Disturbance of the fetal thyroid hormone state has long-term consequences for treatment of thyroidal and central congenital hypothyroidism.

M. Kempers, E. Endert, A. V. van Trotsenburg, 2005, The Journal of clinical endocrinology and metabolism.

A negative iodine balance is found in healthy neonates compared with neonates with thyroid agenesis.

H. Oosting, B. Bakker, J. de Vijlder, 1999, The Journal of endocrinology.

Congenital hypothyroidism in two cats due to defective organification: data suggesting loosely anchored thyroperoxidase.

J. de Vijlder, A. Rijnberk, J. V. van Dijk, 1991, Acta endocrinologica.

On the origin of circulating thyroglobulin.

C. Ris-Stalpers, J. de Vijlder, T. Vulsma, 1999, European journal of endocrinology.

Cloning of tissue-specific genes using serial analysis of gene expression and a novel computational substraction approach.

A. V. van Kampen, A. V. Kampen, C. Ris-Stalpers, 2001, Genomics.

Frequent adverse events after treatment for childhood-onset differentiated thyroid carcinoma: a single institute experience.

H. V. van Santen, J. de Vijlder, T. Vulsma, 2004, European journal of cancer.

Production of monoclonal antibodies to thyroglobulin by in vitro immunization with a free synthetic peptide.

M. de Boer, F. Ossendorp, J. de Vijlder, 1987, Molecular immunology.

A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism.

F. Baas, J. de Vijlder, T. Vulsma, 1994, The Journal of clinical endocrinology and metabolism.

Normal-sized thyroglobulin messenger ribonucleic acid in Dutch goats with a thyroglobulin synthesis defect is translated into a 35,000 molecular weight N-terminal fragment.

J. de Vijlder, J. V. van Dijk, A. Sterk, 1989, Endocrinology.

Importance of the content and localization of tyrosine residues for thyroxine formation within the N-terminal part of human thyroglobulin.

C. Ris-Stalpers, J. de Vijlder, O. Bakker, 1995, European journal of endocrinology.

The Effect of Life-long Thyroxine Treatment and Physical Activity on Bone Mineral Density in Young Adult Women with Congenital Hypothyroidism

M. Kempers, H. Verberne, B. van Eck-Smit, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Binding of NAD+ to rabbit-muscle glyceraldehydephosphate dehydrogenase as studied by optical rotatory dispersion and circular dichroism.

B. Harmsen, J. de Vijlder, 1969, Biochimica et biophysica acta.

[Evaluation of a decade of neonatal screening for congenital hypothyroidism in The Netherlands].

J. Loeber, J. de Vijlder, T. Vulsma, 1993, Nederlands tijdschrift voor geneeskunde.

The role of serum thyroglobulin concentration and thyroid ultrasound imaging in the detection of iodide transport defects in infants.

J. de Vijlder, T. Vulsma, M. Gons, 1991, Acta endocrinologica.

Inhibition of T3-receptor binding by Nitrofen.

D. Tibboel, W. Wiersinga, J. de Vijlder, 1994, Biochimica et biophysica acta.

Characterization of five monoclonal antibodies obtained after immunization in vitro with a synthetic 19-amino acid peptide of thyroglobulin.

P. Admiraal, M. de Boer, F. Ossendorp, 1987, Hybridoma.

Generation and characterization of monoclonal antibodies directed against noniodinated and iodinated thyroglobulin, among which are antibodies against hormonogenic sites.

M. de Boer, J. de Vijlder, M. D. den Hartog, 1990, Endocrinology.

TSH action on iodination in FRTL-5 cells.

F. Ossendorp, J. de Vijlder, L. M. Leer, 1990, Hormone and metabolic research. Supplement series.

The reaction between NAD+ and rabbit-muscle glyceraldehydephosphate dehydrogenase.

E. C. Slater, J. de Vijlder, E. Slater, 1968, Biochimica et biophysica acta.

Thyroid function in preterm newborns; is T4 treatment required in infants < 27 weeks' gestational age?

A. V. van Baar, J. Kok, A. van Wassenaer, 2009, Experimental and clinical endocrinology & diabetes.

Thyroxine administration to infants of less than 30 weeks' gestational age does not increase plasma triiodothyronine concentrations.

E. Endert, J. Kok, A. van Wassenaer, 1993, Acta endocrinologica.