检索结果 - 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 由 Jan M. Wit, Gerdine A. Kamp, Wilma Oostdijk

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

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

    出版 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 由 Jan M. Wit, Wilma Oostdijk, Monique Losekoot, Hermine A. van Duyvenvoorde, Claudia Ruivenkamp, Sarina G. Kant

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

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

    出版 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 由 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

    出版 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. 由 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

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 2015
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  17. 17
    Central 22q11.2 deletions

    Central 22q11.2 deletions 由 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

    出版 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 由 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

    出版 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 由 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

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

    Copy number variants in patients with short stature 由 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

    出版 2013
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