Search Results - Wilma Oostdijk

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  1. 1
    Towards a Rational and Efficient Diagnostic Approach in Children Referred for Growth Failure to the General Paediatrician

    Towards a Rational and Efficient Diagnostic Approach in Children Referred for Growth Failure to the General Paediatrician by Jan M. Wit, Gerdine A. Kamp, Wilma Oostdijk

    Published 2019
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  2. 2
    Diagnostic Approach in Children with Short Stature

    Diagnostic Approach in Children with Short Stature by Wilma Oostdijk, Floor K Grote, Sabine M.P.F. de Muinck Keizer‐Schrama, Jan M. Wit

    Published 2009
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  3. 3
    MECHANISMS IN ENDOCRINOLOGY: Novel genetic causes of short stature

    MECHANISMS IN ENDOCRINOLOGY: Novel genetic causes of short stature by Jan M. Wit, Wilma Oostdijk, Monique Losekoot, Hermine A. van Duyvenvoorde, Claudia Ruivenkamp, Sarina G. Kant

    Published 2015
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  4. 4
    Pubertal Development in The Netherlands 1965–1997

    Pubertal Development in The Netherlands 1965–1997 by Dick Mul, A.M. Fredriks, Stef van Buuren, Wilma Oostdijk, S.P. Verloove-Vanhorick, Jan M. Wit

    Published 2001
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  5. 5
    Developing evidence-based guidelines for referral for short stature

    Developing evidence-based guidelines for referral for short stature by Floor K Grote, Paula van Dommelen, Wilma Oostdijk, Sabine M.P.F. de Muinck Keizer‐Schrama, P.H. Verkerk, Jan M. Wit, Stef van Buuren

    Published 2007
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  6. 6
    Final height in central precocious puberty after long term treatment with a slow release GnRH agonist.

    Final height in central precocious puberty after long term treatment with a slow release GnRH agonist. by Wilma Oostdijk, B. Rikken, S Schreuder, B.J. Otten, Roelof J. Odink, C. Rouwé, M. Jansen, Willem J.M. Gerver, J. J. J. Waelkens, Stenvert L. S. Drop

    Published 1996
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  7. 7
    The diagnostic work up of growth failure in secondary health care; An evaluation of consensus guidelines

    The diagnostic work up of growth failure in secondary health care; An evaluation of consensus guidelines by Floor K Grote, Wilma Oostdijk, S M de Muinck Keizer-Schrama, Paula van Dommelen, Stef van Buuren, Friedo W. Dekker, A. G. Ketel, Henriëtte A. Moll, Jan M. Wit

    Published 2008
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  8. 8
    Inhibition of Gsk3β in cartilage induces osteoarthritic features through activation of the canonical Wnt signaling pathway

    Inhibition of Gsk3β in cartilage induces osteoarthritic features through activation of the canonical Wnt signaling pathway by Razvan L. Miclea, M. Siebelt, Livio Finos, Jelle J. Goeman, Clemens W.G.M. Löwik, Wilma Oostdijk, Harrie Weinans, Jan M. Wit, Els C. Robanus-Maandag, Marcel Karperien

    Published 2011
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  9. 9
    Phenotypic Features and Response to GH Treatment of Patients With a Molecular Defect of the IGF-1 Receptor

    Phenotypic Features and Response to GH Treatment of Patients With a Molecular Defect of the IGF-1 Receptor by M.J.E. Walenkamp, Jasmijn M L Robers, Jan M. Wit, Gladys R.J. Zandwijken, Hermine A. van Duyvenvoorde, Wilma Oostdijk, Anita Hokken-Koelega, Sarina G. Kant, Monique Losekoot

    Published 2019
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  10. 10
    Long‐term results of growth hormone therapy in children with short stature, subnormal growth rate and normal growth hormone response to secretagogues

    Long‐term results of growth hormone therapy in children with short stature, subnormal growth rate and normal growth hormone response to secretagogues by J.M. Wit, Bart Boersma, Sabine M.P.F. de Muinck Keizer‐Schrama, Henrlët E. Nienhuls, Wilma Oostdijk, Barto J. Otten, Henriëtte A. Delemarre‐van de Waal, Maarten Reeser, J. J. J. Waelkens, Berthon Rikken, Guy Massa

    Published 1995
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  11. 11
    Short Stature Associated with a Novel Heterozygous Mutation in the<i>Insulin-Like Growth Factor 1</i>Gene

    Short Stature Associated with a Novel Heterozygous Mutation in the<i>Insulin-Like Growth Factor 1</i>Gene by Hermine A. van Duyvenvoorde, P.A. van Setten, M.J.E. Walenkamp, J. van Doorn, Jens Koenig, Lisbeth Gauguin, Wilma Oostdijk, Claudia Ruivenkamp, Monique Losekoot, John D. Wade, Pierre De Meyts, Marcel Karperien, C. Noordam, Jan M. Wit

    Published 2010
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  12. 12
    Novel Leptin Receptor Mutations Identified in Two Girls with Severe Obesity Are Associated with Increased Bone Mineral Density

    Novel Leptin Receptor Mutations Identified in Two Girls with Severe Obesity Are Associated with Increased Bone Mineral Density by Sabine E Hannema, Jan M. Wit, Mieke E.C.A.M. Houdijk, Arie van Haeringen, Elsa C. Bik, Annemieke J.M.H. Verkerk, André G. Uitterlinden, Sarina G. Kant, Wilma Oostdijk, Egbert Bakker, Henriëtte A. Delemarre‐van de Waal, Monique Losekoot

    Published 2016
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  13. 13
    IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management

    IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management by Sjoerd D. Joustra, Charlotte A. Heinen, Nadia Schoenmakers, Marco Bonomi, Bart E.P.B. Ballieux, Marc‐Olivier Turgeon, Daniel J. Bernard, Eric Fliers, A.S. Paul van Trotsenburg, Monique Losekoot, Luca Persani, Jan M. Wit, Nienke R. Biermasz, Alberto M. Pereira, Wilma Oostdijk

    Published 2016
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  14. 14
    PAPSS2 Deficiency Causes Androgen Excess via Impaired DHEA Sulfation—In Vitro and in Vivo Studies in a Family Harboring Two Novel PAPSS2 Mutations

    PAPSS2 Deficiency Causes Androgen Excess via Impaired DHEA Sulfation—In Vitro and in Vivo Studies in a Family Harboring Two Novel PAPSS2 Mutations by Wilma Oostdijk, Jan Idkowiak, Jonathan Wolf Mueller, Philip J House, Angela E. Taylor, Michael O’Reilly, Beverly Hughes, Martine C. de Vries, Sarina G. Kant, Gijs W.E. Santen, Annemieke J.M.H. Verkerk, André G. Uitterlinden, Jan M. Wit, Monique Losekoot, Wiebke Arlt

    Published 2015
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  15. 15
    Genotype<i>Versus</i>Phenotype in Families with Androgen Insensitivity Syndrome

    Genotype<i>Versus</i>Phenotype in Families with Androgen Insensitivity Syndrome by Annemie L. M. Boehmer, Hennie T. Brüggenwirth, Cissy van Assendelft, Barto J. Otten, M.C.T. Verleun-Mooijman, Martinus F. Niermeijer, Han G. Brunner, Catrienus W. Rouwé, J. J. J. Waelkens, Wilma Oostdijk, Wim J. Kleijer, Theodorus van der Kwast, Monique A. de Vroede, Stenvert L. S. Drop

    Published 2001
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  16. 16
    A novel variant of FGFR3 causes proportionate short stature

    A novel variant of FGFR3 causes proportionate short stature by Sarina G. Kant, Iveta Cervenkova, Lukáš Bálek, Lukáš Trantı́rek, Gijs W.E. Santen, Martine C. de Vries, Hermine A. van Duyvenvoorde, Michiel J.R. van der Wielen, Annemieke J.M.H. Verkerk, André G. Uitterlinden, Sabine E Hannema, Jan M. Wit, Wilma Oostdijk, Pavel Krejčı́, Monique Losekoot

    Published 2015
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  17. 17
    Central 22q11.2 deletions

    Central 22q11.2 deletions by Patrick Rump, Nicole de Leeuw, Anthonie J. van Essen, Corien C. Verschuuren‐Bemelmans, Hermine E. Veenstra‐Knol, Mariëlle E.M. Swinkels, Wilma Oostdijk, Claudia Ruivenkamp, William Reardon, Sonja de Munnik, Mariken Ruiter, Ayala Frumkin, Dorit Lev, Christina Evers, Birgit Sikkema‐Raddatz, Trijnie Dijkhuizen, Conny M.A. van Ravenswaaij‐Arts

    Published 2014
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  18. 18
    Adult Height in Short Children Born SGA Treated with Growth Hormone and Gonadotropin Releasing Hormone Analog: Results of a Randomized, Dose-Response GH Trial

    Adult Height in Short Children Born SGA Treated with Growth Hormone and Gonadotropin Releasing Hormone Analog: Results of a Randomized, Dose-Response GH Trial by Annemieke J. Lem, Daniëlle C M van der Kaay, Maria de Ridder, Willie M. Bakker‐van Waarde, Flip J. P. C. M. van der Hulst, Jaap C. Mulder, C. Noordam, Roel J. H. ODINK, Wilma Oostdijk, Eelco J. Schroor, Eric J. Sulkers, Ciska Westerlaken, Anita C. S. Hokken‐Koelega

    Published 2012
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  19. 19
    An Activating Mutation in the Kinase Homology Domain of the Natriuretic Peptide Receptor-2 Causes Extremely Tall Stature Without Skeletal Deformities

    An Activating Mutation in the Kinase Homology Domain of the Natriuretic Peptide Receptor-2 Causes Extremely Tall Stature Without Skeletal Deformities by Sabine E Hannema, Hermine A. van Duyvenvoorde, Thomas Premsler, Ruey‐Bing Yang, Thomas D. Mueller, Birgit Gaßner, Heike Oberwinkler, Ferdinand Roelfsema, Gijs W.E. Santen, Timothy C. R. Prickett, Sarina G. Kant, Annemieke J.M.H. Verkerk, André G. Uitterlinden, Eric A. Espiner, Claudia Ruivenkamp, Wilma Oostdijk, Alberto M. Pereira, Monique Losekoot, Michaela Kühn, Jan M. Wit

    Published 2013
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  20. 20
    Copy number variants in patients with short stature

    Copy number variants in patients with short stature by Hermine A. van Duyvenvoorde, Julian C. Lui, Sarina G. Kant, Wilma Oostdijk, Antoinet C.J. Gijsbers, Mariëtte J.V. Hoffer, Marcel Karperien, M.J.E. Walenkamp, C. Noordam, Paul G. Voorhoeve, Verónica Mericq, Alberto M. Pereira, Hedi L Claahsen-van de Grinten, Sandy A. van Gool, Martijn H. Breuning, Monique Losekoot, Jeffrey Baron, Claudia Ruivenkamp, Jan M. Wit

    Published 2013
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