Zobrazeno 1 - 10
of 93
pro vyhledávání: '"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
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
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
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
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’
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
Publikováno v:
Nucleic Acids Research, 29(8), 1690-1694. Oxford University Press
Scopus-Elsevier
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
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
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
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
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