Zobrazeno 1 - 10 of 268 pro vyhledávání: '"T, Vulsma"'
1
Quality of life, developmental milestones, and self-esteem of young adults with congenital hypothyroidism diagnosed by neonatal screening
Autor: L. van der Sluijs Veer, M. J. E. Kempers, B. F. Last, T. Vulsma, M. A. Grootenhuis
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
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccad40591195a50dceed2010a6eac64a
https://doi.org/10.1210/jc.2007-1560
Zobrazit plný text záznamu
2
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
Zobrazit plný text záznamu
3
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
Zobrazit plný text záznamu
4
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
Zobrazit plný text záznamu
5
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
Zobrazit plný text záznamu
6
High incidence of thyroid dysfunction despite prophylaxis with potassium iodide during 131I-meta-iodobenzylguanidine treatment in children with neuroblastoma
Autor: Jan de Kraker, T. Vulsma, Hanneke M. van Santen, Berthe L. van Eck, Jan J. M. de Vijlder
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbb95a663c3d710757ed3ba0bbc66a15
https://doi.org/10.1002/cncr.10447
Zobrazit plný text záznamu
7
Adult height and age at menarche in childhood cancer survivors
Autor: H. Behrendt, E.M. Noorda, T. Vulsma, F.E. van Leeuwen, R. Somers
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1f01c7452939a9de84c064c529ec01b
https://doi.org/10.1016/s0959-8049(00)00438-x
Zobrazit plný text záznamu
8
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
Zobrazit plný text záznamu
9
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
Zobrazit plný text záznamu
10
Successful transfer to sulfonylurea therapy in an infant with developmental delay, epilepsy and neonatal diabetes (DEND) syndrome and a novel ABCC8 gene mutation
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
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84f39fcce27da6c605bf00193158e48b
http://europepmc.org/articles/PMC3017308
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje