Zobrazeno 1 - 10
of 268
pro vyhledávání: '"T. Vulsma"'
Publikováno v:
van der Sluijs Veer, L, Kempers, M J, Last, B F, Vulsma, T & Grootenhuis, M A 2008, ' Quality of life, developmental milestones, and self-esteem of young adults with congenital hypothyroidism diagnosed by neonatal screening ', Journal of Clinical Endocrinology and Metabolism, vol. 93, no. 7, pp. 2654-2661 . https://doi.org/10.1210/jc.2007-1560
Journal of Clinical Endocrinology and Metabolism, 93, 7, pp. 2654-61
Journal of Clinical Endocrinology and Metabolism, 93, 2654-61
Journal of Clinical Endocrinology and Metabolism, 93(7), 2654-2661. Oxford University Press
Journal of clinical endocrinology and metabolism, 93(7), 2654-2661. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 93, 7, pp. 2654-61
Journal of Clinical Endocrinology and Metabolism, 93, 2654-61
Journal of Clinical Endocrinology and Metabolism, 93(7), 2654-2661. Oxford University Press
Journal of clinical endocrinology and metabolism, 93(7), 2654-2661. The Endocrine Society
Contains fulltext : 71281.pdf (Publisher’s version ) (Closed access) CONTEXT: With advances in the treatment of congenital hypothyroidism (CH), the neuropsychological functioning of CH patients is considerably improved. Although much is written abo
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:
Cancer, 94(7), 2081-2089. John Wiley and Sons Inc.
BACKGROUND Treatment modalities like targeted radiotherapy with 131I-meta-iodobenzylguanidine (131I-MIBG) improve survival rates after neuroblastoma (NB). Radiation to the thyroid gland can lead to hypothyroidism and even malignancy. Because hypothyr
Publikováno v:
European journal of cancer (Oxford, England, 37(5), 605-612. Elsevier Limited
The aim of this study was to assess the long-term effects of cancer treatments on adult height and age at menarche in survivors of various types of childhood cancer. 285 childhood cancer survivors (161 men and 124 women), at least 18 years old and ha
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:
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
Autor:
Annabelle S. Slingerland, C. Ris-Stalpers, T. Vulsma, Nitash Zwaveling-Soonawala, E. E. Hagebeuk, A. S. P. van Trotsenburg
Publikováno v:
Diabetologia
Diabetologia, 54(2), 469-471. Springer Verlag
Diabetologia, 54(2), 469-471. Springer Verlag
To the Editor: Permanent neonatal diabetes mellitus (PNDM) is mainly caused by activating mutations in the KCNJ11 or ABCC8 genes, encoding respectively the Kir6.2 and sulfonylurea receptor (SUR)1 subunits of the KATP channels in the pancreatic beta c