检索结果 - C. Noordam

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  1. 1
    Growth, Endocrine Features, and Growth Hormone Treatment in Noonan Syndrome

    Growth, Endocrine Features, and Growth Hormone Treatment in Noonan Syndrome 由 Jovanna Dahlgren, C. Noordam

    出版 2022
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  2. 2
    Prader–Willi Syndrome and Hypogonadism: A Review Article

    Prader–Willi Syndrome and Hypogonadism: A Review Article 由 C. Noordam, Charlotte Höybye, Urs Eiholzer

    出版 2021
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  3. 3
    Response to Growth Hormone Treatment and Final Height in Noonan Syndrome in a Large Cohort of Patients in the KIGS Database

    Response to Growth Hormone Treatment and Final Height in Noonan Syndrome in a Large Cohort of Patients in the KIGS Database 由 Renske Raaijmakers, C. Noordam, Georgios Karagiannis, J W Gregory, Niels Thomas Hertel, Ilkka Sipilä, B. Otten

    出版 2008
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  4. 4
    The occurrence of lipidic particles in lipid bilayers as seen by 31P NMR and freeze-fracture electron-microscopy

    The occurrence of lipidic particles in lipid bilayers as seen by 31P NMR and freeze-fracture electron-microscopy 由 Ben de Kruijff, A. J. Verkley, Cees J. A. van Echteld, W.J. Gerritsen, C. Mombers, P.C. Noordam, J. de Gier

    出版 1979
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  5. 5
    Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births

    Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births 由 A. S. Slingerland, Beverley Shields, Sarah E. Flanagan, G.J. Bruining, C. Noordam, Agnieszka Gach, Wojciech Młynarski, Maciej T. Małecki, Andrew T. Hattersley, Sian Ellard

    出版 2009
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  6. 6
    Inactivating<i>PAPSS2</i>Mutations in a Patient with Premature Pubarche

    Inactivating<i>PAPSS2</i>Mutations in a Patient with Premature Pubarche 由 C. Noordam, Vivek Dhir, Joanne McNelis, Florian Schlereth, Neil A. Hanley, Nils Krone, Jan Smeitink, Roel Smeets, Fred C.G.J. Sweep, Hedi L. Claahsen‐van der Grinten, Wiebke Arlt

    出版 2009
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  7. 7
    Insights Into the Biochemical and Genetic Basis of Glucokinase Activation From Naturally Occurring Hypoglycemia Mutations

    Insights Into the Biochemical and Genetic Basis of Glucokinase Activation From Naturally Occurring Hypoglycemia Mutations 由 Anna L. Gloyn, C. Noordam, Michèl A.A.P. Willemsen, Sian Ellard, Wayne Lam, Ian W Campbell, Paula Midgley, Chyio Shiota, Carol Buettger, Mark A. Magnuson, Franz M. Matschinsky, Andrew T. Hattersley

    出版 2003
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  8. 8
    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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  9. 9
    Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation

    Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation 由 Marjolijn C.J. Jongmans, Ineke van der Burgt, Peter M. Hoogerbrugge, C. Noordam, Helger G. Yntema, Willy M. Nillesen, Roland P Kuiper, Marjolijn J. L. Ligtenberg, Ad Geurts van Kessel, J. Han van Krieken, Lambertus A. Kiemeney, Nicoline Hoogerbrugge

    出版 2011
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  10. 10
    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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  11. 11
    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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  12. 12
    Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by<i>TPIT</i>Gene Mutations

    Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by<i>TPIT</i>Gene Mutations 由 Sophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino, Magali Gueydan, Anne Barlier, M David, Marc Nicolino, G Malpuech, Pierre Déchelotte, Cheri Deal, Guy Van Vliet, Monique De Vroede, Felix G. Riepe, Carl‐Joachim Partsch, Wolfgang G. Sippell, Merih Berberoğlu, Begüm Atasay, Francis de Zegher, Dominique Beckers, Jennifer Kyllo, Patricia A. Donohoue, Martin Faßnacht, Stefanie Hahner, Bruno Allolio, C. Noordam, Leo Dunkel, Matti Hero, B. Pigeon, Jacques Weill, Sevket Yigit, Raja Brauner, Juan J. Heinrich, Elizabeth A. Cummings, Christie Riddell, A Enjalbert, Jacques Drouin

    出版 2005
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