Zobrazeno 1 - 10 of 648 pro vyhledávání: '"J.M. Wit"'
1
De richtlijn lengtegroei voor de jeugdgezondheidszorg
Autor: namens de leden van de werkgroep, T. de Jong, K. Bisschoff, M. Beltman, M. Gianotten, J.M. Wit, E. A. Lindhout-Hoogendoorn, J.A. de Wilde, T. Steenbergen, J. van de Laar, Wilma Oostdijk, Anita C. S. Hokken-Koelega, P. van Dommelen, M. Oostdijk-van den Berg, R. van Zoonen, E. Vlasblom, I. van Zon, F K Grote
Publikováno v: JGZ Tijdschrift voor jeugdgezondheidszorg. 53:130-137
Inleiding: Het doel van dit onderzoek was het ontwikkelen van een richtlijn voor Jeugdgezondheidszorg (JGZ)-professionals om aandoeningen die samenhangen met een kleine lengte (en/of trage groei) of een grote lengte (en/of snelle groei) vroegtijdig o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::88d37c04be5ada8416473ee129c3cc0e
https://doi.org/10.1007/s12452-021-00264-5
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2
A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency
Autor: M J E Walenkamp, J.M. Wit
Publikováno v: European Journal of Endocrinology, 181(6), C29-C33. BioScientifica Ltd.
Walenkamp, M J E & Wit, J M 2019, ' A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency ', European Journal of Endocrinology, vol. 181, no. 6, pp. C29-C33 . https://doi.org/10.1530/EJE-19-0801
European Journal of Endocrinology, 181(6), C29-C33
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d54764a163ea0f3bcaa389ac9be20f7
https://hdl.handle.net/1887/3195451
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4
IGF-1 and IGF-1 SDS - Fit for purpose?
Autor: Wilma Oostdijk, Christa M. Cobbaert, Bart E.P.B. Ballieux, Nienke R. Biermasz, J.M. Wit, T M Kuijper, S Kos, Hannema Se
Publikováno v: Kos, S, Cobbaert, C M, Kuijper, T M, Oostdijk, W, Hannema, S E, Wit, J M, Biermasz, N & Ballieux, B E P B 2019, ' IGF-1 and IGF-1 SDS-Fit for purpose? ', European Journal of Endocrinology, vol. 181, no. 5, pp. L1-L4 . https://doi.org/10.1530/EJE-19-0458
European Journal of Endocrinology, 181(5), L1-L4
European Journal of Endocrinology, 181(5), L1-L4. BioScientifica Ltd.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d671ff0de7912971ccfb3c10137e80f
https://research.vumc.nl/en/publications/be409ffc-8670-4751-9497-d059655721a3
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5
Normale groei en ontwikkeling
Autor: J.M. Wit, H.A. Delemarre-van de Waal, Joost Rotteveel
Publikováno v: Kindergeneeskunde voor kinderverpleegkundigen ISBN: 9789036818506
Kindergeneeskunde voor kinderverpleegkundigen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::83a2ce36494373040e722c5cc17aae5c
https://doi.org/10.1007/978-90-368-1851-3_5
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6
Pharmacokinetics and Pharmacodynamics of Orally Administered Clonidine: A Model-Based Approach
Autor: Jacobus Burggraaf, Rám N. Sukhai, Boudewijn Bakker, Adam F. Cohen, H M Reeser, P Hu, Erica S. Klaassen, Richard H. Klein, B E P B Ballieux, Wilma Oostdijk, Ricardo Alvarez-Jimenez, J.M. Wit, Jan Freijer
Publikováno v: Hormone Research in Paediatrics, 79(5), 300-309
Klein, R H, Alvarez-Jimenez, R, Sukhai, R N, Oostdijk, W, Bakker, B, Reeser, H M, Ballieux, B E P B, Hu, P, Klaassen, E S, Freijer, J, Burggraaf, J, Cohen, A F & Wit, J M 2013, ' Pharmacokinetics and pharmacodynamics of orally administered clonidine : A model-based approach ', Hormone Research in Paediatrics, vol. 79, no. 5, pp. 300-309 . https://doi.org/10.1159/000350819
Hormone Research in Paediatrics, 79(5), 300-309. S. Karger AG
Background/Aims: The oral clonidine test is a diagnostic procedure performed in children with suspected growth hormone (GH) deficiency. It is associated with untoward effects, including bradycardia, hypotension and sedation. Serum clonidine levels ha
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7ee96142c04000c934356ab6b152d5e
https://doi.org/10.1159/000350819
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7
The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients
Autor: Irene Campi, Marcel M.A.M. Mannens, M.H. Breuning, Mehul T. Dattani, Marco Bonomi, Giorgio Radetti, W. Oostdijk, Daniel J. Bernard, Krishna Chatterjee, Nadia Schoenmakers, Joseph A M J L Janssen, H. Zhu, Paolo Beck-Peccoz, Sjoerd D. Joustra, Maria Paola Lombardi, J.M. Wit, Erik Endert, Raoul C.M. Hennekam, Nienke R. Biermasz, Natasha M. Appelman-Dijkstra, Yu Sun, Aimee J. Varewijck, Alberto M. Pereira, Charlotte A Heinen, A S P van Trotsenburg, Eleonora P M Corssmit, Luca Persani, Timothy M. E. Davis, Beata Bak
Publikováno v: Journal of clinical endocrinology and metabolism, 98(12), 4942-4952. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 98(12), 4942-4952. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 98(12), 4942-4952
Context: Ig superfamily member1 (IGSF1) deficiency was recently discovered as a novel X-linked cause of central hypothyroidism (CeH) and macro-orchidism. However, clinical and biochemical data regarding growth, puberty, and metabolic outcome, as well
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17eb6e22e0801827994fba2a88dfa2d8
https://pure.eur.nl/en/publications/51ed2254-11a0-4202-8c57-63351e3c7191
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8
What Constitutes the Best Interest of a Child? Views of Parents, Children, and Physicians in a Pediatric Oncology Setting
Autor: J.M. Wit, Gertjan J.L. Kaspers, Dorine Bresters, M.C. de Vries, E. F. Van Leeuwen, Mirjam Houtlosser, Dirk P Engberts
Publikováno v: Ajob Primary Research, 4, 2, pp. 1-10
Ajob Primary Research, 4, 1-10
de Vries, M C, Bresters, D, Kaspers, G J L, Houtlosser, M, Wit, J M, Engberts, D P & van Leeuwen, E 2013, ' What Constitutes the Best Interest of a Child? Views of Parents, Children, and Physicians in a Pediatric Oncology Setting ', AJOB Primary Research, vol. 4, no. 2, pp. 1-10 . https://doi.org/10.1080/21507716.2012.757254
AJOB Primary Research, 4(2), 1-10. Taylor and Francis Ltd.
Background: In pediatrics, the “best interest” standard has become the prevailing standard in decision making even though it proves difficult to apply in practice. Differences in values can lead to different views by families and physicians of wh
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7839e02781fd01c7911c9bc894089c3
https://doi.org/10.1080/21507716.2012.757254
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9
Splice Site Mutations in GH1 Detected in Previously (Genetically) Undiagnosed Families with Congenital Isolated Growth Hormone Deficiency Type II
Autor: Monique Losekoot, M. de Vroede, Barto J. Otten, J. Alfen-van der Velden, Ronald A.J. Duim, Marlies Kempers, J.M. Wit, S.N. van der Crabben, Romana T. Netea-Maier
Publikováno v: Hormone Research in Paediatrics. 80:390-396
Background: Congenital isolated growth hormone deficiency (IGHD) is a rare endocrine disorder that presents with severe proportionate growth failure. Dominant (type II) IGHD is usually caused by heterozygous mutations of GH1. The presentation of newl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9267b87e26422cdddf1d74b8e7f2bbb5
https://doi.org/10.1159/000355403
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10
Mild deficits in attentional control in patients with the IGSF1 deficiency syndrome
Autor: Wilma Oostdijk, Cornelie D. Andela, Huub A. M. Middelkoop, Nienke R. Biermasz, J.M. Wit, A S P van Trotsenburg, Sjoerd D. Joustra, Ellen A. Fliers, Alberto M. Pereira
Publikováno v: Clinical Endocrinology, 84(6), 896-903
Clinical Endocrinology, 84(6), 896-903. WILEY-BLACKWELL
Clinical endocrinology, 84(6), 896-903
Clinical endocrinology, 84(6), 896-903. Wiley-Blackwell
SummaryObjective Male patients with the X-linked IGSF1 deficiency syndrome are characterized by central hypothyroidism, delayed pubertal testosterone rise, adult macroorchidism, variable prolactin deficiency and occasionally transient partial growth
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d507bb133d4730c95cfc5f7a3ce3465d
http://hdl.handle.net/1887/113956
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