Zobrazeno 1 - 10
of 564
pro vyhledávání: '"Hoorweg-Nijman"'
Autor:
Wessels, Margreet, Velthuis, Anouk, van Lochem, Ellen, Duijndam, Eline, Hoorweg-Nijman, Gera, de Kruijff, Ineke, Wolters, Victorien, Berghout, Eveline, Meijer, Jos, Bokma, Jan Alle, Mul, Dick, van der Velden, Janielle, Roovers, Lian, Mearin, M. Luisa, van Setten, Petra
Publikováno v:
In The Journal of Pediatrics August 2020 223:87-92
Autor:
Gera Hoorweg-Nijman, Anita C. S. Hokken-Koelega, Martijn J. J. Finken, Mariette van Leeuwen, Stephany Donze, Gianni Bocca, Petr E. Jira, Janiëlle A E M van Alfen-van der Velden, Layla Damen
Publikováno v:
Clinical Endocrinology, 91(1), 118-123. Wiley
Clinical Endocrinology, 91, 118-123
Clinical Endocrinology, 91, 1, pp. 118-123
Clinical Endocrinology, 91(1), 118-123. Wiley-Blackwell Publishing Ltd
Donze, S H, Damen, L, van Alfen-van der Velden, J A E M, Bocca, G, Finken, M J J, Hoorweg-Nijman, G J G, Jira, P E, van Leeuwen, M & Hokken-Koelega, A C S 2019, ' Prevalence of growth hormone (GH) deficiency in previously GH-treated young adults with Prader-Willi syndrome ', Clinical Endocrinology, vol. 91, no. 1, pp. 118-123 . https://doi.org/10.1111/cen.13988
Clinical Endocrinology
Clinical Endocrinology, 91(1), 118-123. Wiley-Blackwell
Clinical Endocrinology, 91, 118-123
Clinical Endocrinology, 91, 1, pp. 118-123
Clinical Endocrinology, 91(1), 118-123. Wiley-Blackwell Publishing Ltd
Donze, S H, Damen, L, van Alfen-van der Velden, J A E M, Bocca, G, Finken, M J J, Hoorweg-Nijman, G J G, Jira, P E, van Leeuwen, M & Hokken-Koelega, A C S 2019, ' Prevalence of growth hormone (GH) deficiency in previously GH-treated young adults with Prader-Willi syndrome ', Clinical Endocrinology, vol. 91, no. 1, pp. 118-123 . https://doi.org/10.1111/cen.13988
Clinical Endocrinology
Clinical Endocrinology, 91(1), 118-123. Wiley-Blackwell
OBJECTIVE: Some features of subjects with Prader-Willi syndrome (PWS) resemble those seen in growth hormone deficiency (GHD). Children with PWS are treated with growth hormone (GH), which has substantially changed their phenotype. Currently, young ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::552835ff4798d883669ccbafe26dea8a
https://hdl.handle.net/2066/204782
https://hdl.handle.net/2066/204782
Autor:
Margreet Wessels, Anouk Velthuis, Ellen van Lochem, Eline Duijndam, Gera Hoorweg-Nijman, Ineke de Kruijff, Victorien Wolters, Eveline Berghout, Jos Meijer, Jan Alle Bokma, Dick Mul, Janielle van der Velden, Lian Roovers, M. Luisa Mearin, Petra van Setten
Publikováno v:
The Journal of Pediatrics. 246:293
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb3777a132cf74ff2ad75b8b0a1e712a
https://doi.org/10.1016/j.jpeds.2022.04.033
https://doi.org/10.1016/j.jpeds.2022.04.033
Autor:
Yvonne Schönbeck, Annelieke A A van der Linde, Paul H. Verkerk, Roelof Odink, Hedi L Claahsen-van der Grinten, Paul van Trotsenburg, Mirjam E. van Albada, Anita Boelen, Peter C. J. I. Schielen, Saartje Straetemans, Martijn J. J. Finken, Erica L T van den Akker, Hetty J. van der Kamp, Gera Hoorweg-Nijman, Sabine E. Hannema
Publikováno v:
Archives of Disease in Childhood, 104(7), 653-657. BMJ Publishing Group
Archives of Disease in Childhood, 104, 653-657
Archives of Disease in Childhood, 104(7), 653-657. BMJ PUBLISHING GROUP
Archives of Disease in Childhood, 104(7), 653. BMJ Publishing Group
Archives of Disease in Childhood, 104, 7, pp. 653-657
Archives of disease in childhood, 104(7), 653-657. BMJ Publishing Group
van der Linde, A A A, Schönbeck, Y, van der Kamp, H J, van den Akker, E L T, van Albada, M E, Boelen, A, Finken, M J J, Hannema, S E, Hoorweg-Nijman, G, Odink, R J, Schielen, P C J I, Straetemans, S, van Trotsenburg, P S, Claahsen-van der Grinten, H L & Verkerk, P H 2019, ' Evaluation of the Dutch neonatal screening for congenital adrenal hyperplasia ', Archives of Disease in Childhood, vol. 104, no. 7, pp. 653-657 . https://doi.org/10.1136/archdischild-2018-315972, https://doi.org/10.1136/archdischild-2018-315972
Archives of Disease in Childhood, 7, 104, 653-657
Archives of Disease in Childhood, 104(7), 653-657
Archives of Disease in Childhood, 104, 653-657
Archives of Disease in Childhood, 104(7), 653-657. BMJ PUBLISHING GROUP
Archives of Disease in Childhood, 104(7), 653. BMJ Publishing Group
Archives of Disease in Childhood, 104, 7, pp. 653-657
Archives of disease in childhood, 104(7), 653-657. BMJ Publishing Group
van der Linde, A A A, Schönbeck, Y, van der Kamp, H J, van den Akker, E L T, van Albada, M E, Boelen, A, Finken, M J J, Hannema, S E, Hoorweg-Nijman, G, Odink, R J, Schielen, P C J I, Straetemans, S, van Trotsenburg, P S, Claahsen-van der Grinten, H L & Verkerk, P H 2019, ' Evaluation of the Dutch neonatal screening for congenital adrenal hyperplasia ', Archives of Disease in Childhood, vol. 104, no. 7, pp. 653-657 . https://doi.org/10.1136/archdischild-2018-315972, https://doi.org/10.1136/archdischild-2018-315972
Archives of Disease in Childhood, 7, 104, 653-657
Archives of Disease in Childhood, 104(7), 653-657
BackgroundIn 2002, a nationwide screening for congenital adrenal hyperplasia (CAH) was introduced in the Netherlands. The aim of our study is to evaluate the validity of the neonatal screening for CAH and to assess how many newborns with salt-wasting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35f84b09644338ab6d7cec9767921320
http://hdl.handle.net/10029/622765
http://hdl.handle.net/10029/622765
Autor:
Nitash Zwaveling-Soonawala, Dederieke A. M. Festen, R. J. Kuppens, M. van Leeuwen, G. C. B. (Karen) Bindels-de Heus, Danny A. J. P. Haring, Euphemia C. A. M. Houdijk, L. Lunshof, R. J. Odink, R. F. A. Tummers-de Lind van Wijngaarden, Wilma Oostdijk, M. E. J. Wegdam-den Boer, Petr E. Jira, Anita C. S. Hokken-Koelega, J. J. G. Hoorweg-Nijman, Gianni Bocca, Elbrich P. C. Siemensma, A. A. E. M. Van Alfen, Joost Rotteveel, H. Van Wieringen, N. E. Bakker
Publikováno v:
Journal of Clinical Endocrinology and Metabolism, 100(4), 1609-1618. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 100(4), 1609-1618
Bakker, N E, Kuppens, R J, Siemensma, E P C, van Wijngaarden, R F A T, Festen, D A M, Bindels-de Heus, G C B, Bocca, G, Haring, D A J P, Hoorweg-Nijman, J J G, Houdijk, E C A M, Jira, P E, Lunshof, L, Odink, R J, Oostdijk, W, Rotteveel, J, Van Alfen, A A E M, van Leeuwen, M, van Wieringen, H, Wegdam-den Boer, M E J, Zwaveling-Soonawala, N & Hokken-Koelega, A C S 2015, ' Bone Mineral Density in Children and Adolescents With Prader-Willi Syndrome: A Longitudinal Study During Puberty and 9 Years of Growth Hormone Treatment ', Journal of Clinical Endocrinology and Metabolism, vol. 100, no. 4, pp. 1609-1618 . https://doi.org/10.1210/jc.2014-4347
Journal of clinical endocrinology and metabolism, 100(4), 1609-1618. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 100(4), 1609-1618. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 100(4), 1609-1618. ENDOCRINE SOC
Journal of Clinical Endocrinology and Metabolism, 100(4), 1609-1618
Bakker, N E, Kuppens, R J, Siemensma, E P C, van Wijngaarden, R F A T, Festen, D A M, Bindels-de Heus, G C B, Bocca, G, Haring, D A J P, Hoorweg-Nijman, J J G, Houdijk, E C A M, Jira, P E, Lunshof, L, Odink, R J, Oostdijk, W, Rotteveel, J, Van Alfen, A A E M, van Leeuwen, M, van Wieringen, H, Wegdam-den Boer, M E J, Zwaveling-Soonawala, N & Hokken-Koelega, A C S 2015, ' Bone Mineral Density in Children and Adolescents With Prader-Willi Syndrome: A Longitudinal Study During Puberty and 9 Years of Growth Hormone Treatment ', Journal of Clinical Endocrinology and Metabolism, vol. 100, no. 4, pp. 1609-1618 . https://doi.org/10.1210/jc.2014-4347
Journal of clinical endocrinology and metabolism, 100(4), 1609-1618. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 100(4), 1609-1618. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 100(4), 1609-1618. ENDOCRINE SOC
Context: Longitudinal data on bone mineral density(BMD) in children and adolescents with Prader-Willi Syndrome (PWS) during long-term GH treatment are not available.Objective: This study aimed to determine effects of long-term GH treatment and pubert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::094d3564d5c0815aec4d04dea434a57a
https://research.rug.nl/en/publications/57dadd42-1500-468f-bdd8-f5d3b203b148
https://research.rug.nl/en/publications/57dadd42-1500-468f-bdd8-f5d3b203b148
Autor:
Wessels, Margreet, Velthuis, Anouk, van Lochem, Ellen, Duijndam, Eline, Hoorweg-Nijman, Gera, de Kruijff, Ineke, Wolters, Victorien, Berghout, Eveline, Meijer, Jos, Bokma, Jan Alle, Mul, Dick, van der Velden, Janielle, Roovers, Lian, Mearin, M. Luisa, van Setten, Petra
Publikováno v:
In The Journal of Pediatrics July 2022 246:293-293
Autor:
Gera Hoorweg-Nijman, Petra van Setten, Anouk Velthuis, Ineke de Kruijff, Margreet Wessels, Eline Duijndam, Dick Mul, Ellen G van Lochem, Jan Alle Bokma, Janiëlle A E M van Alfen-van der Velden, Jos W. R. Meijer, M. Luisa Mearin, Eveline Berghout, Lian Roovers, Victorien M. Wolters
Publikováno v:
Journal of Pediatrics, 223, 87-+. MOSBY-ELSEVIER
Journal of Pediatrics, 223, pp. 87-92.e1
Journal of Pediatrics, 223, 87-92.e1
Journal of Pediatrics, 223, pp. 87-92.e1
Journal of Pediatrics, 223, 87-92.e1
Objective To study the optimal cut-off value for anti-tissue transglutaminase type 2 IgA antibodies (TG2A) in serum to select for diagnostic small bowel biopsies for celiac disease in children with type 1 diabetes mellitus. Study design Children with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b056099fb0baee6efe6e2f78d0a0a11a
https://doi.org/10.1016/j.jpeds.2020.02.086
https://doi.org/10.1016/j.jpeds.2020.02.086
Autor:
Anita Boelen, A S Paul van Trotsenburg, Nitash Zwaveling-Soonawala, Eric Fliers, Charlotte A Heinen, Marielle Alders, Raoul C.M. Hennekam, Gera Hoorweg-Nijman, Hennie Bikker, Ferdinand Roelfsema, Emmely M de Vries, Erica L T van den Akker, Boudewijn Bakker
Publikováno v:
Journal of Medical Genetics
Journal of Medical Genetics, 55(10), 693-700. BMJ Publishing Group
Journal of Medical Genetics, 55(10), 693-700
Journal of medical genetics, 55(10), 693-700. BMJ Publishing Group
Journal of Medical Genetics, 55(10), 693-700. BMJ Publishing Group
Journal of Medical Genetics, 55(10), 693-700
Journal of medical genetics, 55(10), 693-700. BMJ Publishing Group
BackgroundFour genetic causes of isolated congenital central hypothyroidism (CeH) have been identified, but many cases remain unexplained. We hypothesised the existence of other genetic causes of CeH with a Mendelian inheritance pattern.MethodsWe per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7796ff6ff0ed69d4719527b2bdae4a10
https://hdl.handle.net/1887/86797
https://hdl.handle.net/1887/86797
Autor:
Donze, Stephany H., Damen, Layla, Alfen‐van der Velden, Janiëlle A. E. M., Bocca, Gianni, Finken, Martijn J. J., Hoorweg‐Nijman, Gera J. G., Jira, Petr E., Leeuwen, Mariëtte, Hokken‐Koelega, Anita C. S.
Publikováno v:
Clinical Endocrinology; Jul2019, Vol. 91 Issue 1, p118-123, 6p, 2 Charts, 1 Graph
Autor:
van der Linde, Annelieke A. A., Schönbeck, Yvonne, van der Kamp, Hetty J., van den Akker, Erica L. T., van Albada, Mirjam E., Boelen, Anita, Finken, Martijn J. J., Hannema, Sabine E., Hoorweg-Nijman, Gera, Odink, Roelof J., Schielen, Peter C. J. I., Straetemans, Saartje, van Trotsenburg, Paul S., der Grinten, Hedi L. Claahsen-van, Verkerk, Paul H., Claahsen-van der Grinten, Hedi L
Publikováno v:
Archives of Disease in Childhood; Jul2019, Vol. 104 Issue 7, p653-657, 5p, 3 Charts