Výsledky vyhledávání - "J. J. M. de Vijlder"

Separation of some DL-amino acids into their optical isomers by paper adsorption chromatography

Autor: C.L. De Ligny, J. H. H. G. van Willigen, H. Nieboer, J. J. M. de Vijlder

Publikováno v: Recueil des Travaux Chimiques des Pays-Bas. 82:213-224

A systematic research was made into the conditions producing optimum separation of the optical isomers of amino acids by paper chromatography, using as pilot substances racemic mixtures of the amino acids histidine, tryptophan and kynurenin and metha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5583b829d171c088c5e2bee64aa0579b
https://doi.org/10.1002/recl.19630820214

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

Autor: M. J. E. Kempers, L. van der Sluijs Veer, M. W. G. Nijhuis-van der Sanden, L. Kooistra, B. M. Wiedijk, I. Faber, B. F. Last, J. J. M. de Vijlder, M. A. Grootenhuis, T. Vulsma

Publikováno v: Journal of Clinical Endocrinology and Metabolism, 91, 2, pp. 418-24
Kempers, M J, van der Sluijs Veer, L, Nijhuis-van der Sanden, M W, Kooistra, L, Wiedijk, M, Faber, I, Last, B F, de Vijlder, J J, Grootenhuis, M A & Vulsma, T 2006, ' Intellectual and motor development of young adults with congenital hypothyroidism diagnosed by neonatal screening ', Journal of Clinical Endocrinology and Metabolism, vol. 91, no. 2, pp. 418-424 . https://doi.org/10.1210/jc.2005-1209
Journal of Clinical Endocrinology and Metabolism, 91(2), 418-424. Oxford University Press
Journal of clinical endocrinology and metabolism, 91(2), 418-424. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 91, 418-24

Contains fulltext : 35756.pdf (Publisher’s version ) (Open Access) CONTEXT: Long-term follow-up data on cognitive and motor functioning in adult patients with congenital hypothyroidism, diagnosed by neonatal screening, are scarce. Hence, it is stil

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28c92dd7d7a3e60256909568afb7d459
http://jcem.endojournals.org/cgi/reprint/91/2/418

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Disseminated Medullary Thyroid Carcinoma Despite Early Thyroid Surgery in the Multiple Endocrine Neoplasia-2A Syndrome

Autor: T. Vulsma, M.D. van de Wetering, J. J. M. De Vijlder, H.M. van Santen, A S P van Trotsenburg, F. J. W. Ten Kate, Doron Aronson, Wilmar M. Wiersinga

Publikováno v: Thyroid, 15(5), 485-488. Mary Ann Liebert Inc.

A 5 1/2-year-old boy, with a family history of multiple endocrine neoplasia (MEN)-2A syndrome, was evaluated for presence of MEN-2A and medullary thyroid carcinoma (MTC). DNA diagnostics confirmed MEN-2A. Basal (360 ng/L) and pentagastrin stimulated

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7e6f387a124f0d1d0d9443e89fce5c7
https://doi.org/10.1089/thy.2005.15.485

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

Autor: Egbert Bakker, T. Vulsma, Brenda M. Wiedijk, J. J. M. De Vijlder, D.A. van Tijn, Marlies Kempers, A S P van Trotsenburg, Erik Endert

Publikováno v: Journal of clinical endocrinology and metabolism, 90(7), 4094-4100. The Endocrine Society

Background: During T4 supplementation of patients with thyroidal (primary) congenital hypothyroidism (CH) TSH concentrations are frequently elevated despite free T4 (FT4) concentrations being well within the reference range. To examine the thyroid’

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e122f74109b68d4a4d0879a5173d493f
https://doi.org/10.1210/jc.2005-0197

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

Autor: H.M. van Santen, T. Vulsma, Doron Aronson, R.F.H.M Tummers, C. van den Bos, J. J. M. De Vijlder, M.M. Geenen

Publikováno v: European journal of cancer (Oxford, England, 40(11), 1743-1751. Elsevier Limited

Since the mortality rate for childhood differentiated thyroid carcinoma is nearly zero, the focus must be to minimise morbidity following treatment. Our aim was to analyse early and late adverse events. Twenty-five of 26 children treated between 1962

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::200528a996f46b091258b612d6c49fa9
https://doi.org/10.1016/j.ejca.2004.03.006

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

Autor: Erwin Pauws, S. van de Graaf, Carrie Ris-Stalpers, J. J. M. De Vijlder, A. H. C. van Kampen

Publikováno v: Nucleic Acids Research, 29(8), 1690-1694. Oxford University Press
Scopus-Elsevier
Nucleic acids research, 29(8), 1690-1694. Oxford University Press

The analysis of a human thyroid serial analysis of gene expression (SAGE) library shows the presence of an abundant SAGE tag corresponding to the mRNA of thyroglobulin (TG). Additional, less abundant tags are present that can not be linked to any oth

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20f23df1d1b46743e8a20fdeed301c9a
https://doi.org/10.1093/nar/29.8.1690

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Maternal Isodisomy for Chromosome 2p Causing Severe Congenital Hypothyroidism

Autor: J. J. M. De Vijlder, E J Lommen, M G Schipper, Raoul C.M. Hennekam, Bert N. Bakker, T. Vulsma, Hennie Bikker

Publikováno v: Journal of clinical endocrinology and metabolism, 86(3), 1164-1168. The Endocrine Society

Severe congenital hypothyroidism (CH) due to a total iodide organification defect (TIOD) is usually due to mutations in the thyroid peroxidase (TPO) gene located at chromosome 2p25. A homozygous deletion [DeltaT2512 (codon 808)] in exon 14 was identi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b82e5e96ad7040af892df67fb3beadaf
https://doi.org/10.1210/jcem.86.3.7313

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

Autor: Carrie Ris-Stalpers, M Jedlicková, Erwin Pauws, J. J. M. De Vijlder, José Moreno, A. H. C. van Kampen

Publikováno v: Genomics, 75(1-3), 70-76. Academic Press Inc.

A paradigm of molecular medicine is the identification of functionally specialized genes in the search of defects responsible for human disease. To identify novel genes relevant for thyroid physiology, we applied serial analysis of gene expression (S

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https://doi.org/10.1006/geno.2001.6586

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

Autor: A S P van Trotsenburg, T. Vulsma, CH Konings, J. J. M. De Vijlder, Brenda M. Wiedijk, Carrie Ris-Stalpers

Publikováno v: European journal of endocrinology / European Federation of Endocrine Societies, 144(1), 1-4. BioScientifica Ltd.

OBJECTIVE: Subclinical hypothyroidism occurs in a number of children with Down's syndrome (DS). The reason for the mildly elevated plasma thyrotropin (TSH) concentrations is not known. The present study investigated whether decreased TSH bioactivity

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0919a94f36511342a178f663c5306c98
https://doi.org/10.1530/eje.0.1440001

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

Autor: J. H. Kok, Filip Cools, J. J. M. De Vijlder, A. G. van Wassenaer

Publikováno v: European journal of endocrinology / European Federation of Endocrine Societies, 143(6), 733-740. BioScientifica Ltd.

Objective Evaluation of thyroid hormone response to a single administration of triiodothyronine (T3) early postnatally to premature infants of Design A prospective clinical trial with historical control. Methods Ten infants born Results For the infan

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https://doi.org/10.1530/eje.0.1430733

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