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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 4
2010 2
2011 3
2012 1
2013 2
2014 3
2015 3
2017 2
2018 3
2021 2
2022 1
2023 1
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24 results
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Page 1
Biosimilars: controversies as illustrated by rhGH.
Declerck PJ, Darendeliler F, Góth M, Kolouskova S, Micle I, Noordam C, Peterkova V, Volevodz NN, Zapletalová J, Ranke MB. Declerck PJ, et al. Among authors: noordam c. Curr Med Res Opin. 2010 May;26(5):1219-29. doi: 10.1185/03007991003719642. Curr Med Res Opin. 2010. PMID: 20302553 Review.
Motor performance in children with Noonan syndrome.
Croonen EA, Essink M, van der Burgt I, Draaisma JM, Noordam C, Nijhuis-van der Sanden MWG. Croonen EA, et al. Among authors: noordam c. Am J Med Genet A. 2017 Sep;173(9):2335-2345. doi: 10.1002/ajmg.a.38322. Epub 2017 Jun 19. Am J Med Genet A. 2017. PMID: 28627718
GATA6 haploinsufficiency causes pancreatic agenesis in humans.
Allen HL, Flanagan SE, Shaw-Smith C, De Franco E, Akerman I, Caswell R; International Pancreatic Agenesis Consortium; Ferrer J, Hattersley AT, Ellard S. Allen HL, et al. Nat Genet. 2011 Dec 11;44(1):20-22. doi: 10.1038/ng.1035. Nat Genet. 2011. PMID: 22158542 Free PMC article.
Gonadal Hormone Substitution in People with Prader-Labhart-Willi Syndrome: An International Prader-Willi Syndrome Organisation Survey.
Eiholzer U, Stephan A, Fritz C, Katschnig C, Noordam C; Clinical and Scientific Advisory Board of the International Prader-Willi Syndrome Organisation (IPWSO). Eiholzer U, et al. Among authors: noordam c. Horm Res Paediatr. 2021;94(5-6):176-185. doi: 10.1159/000518342. Epub 2021 Jul 13. Horm Res Paediatr. 2021. PMID: 34348303
Copy number variants in patients with short stature.
van Duyvenvoorde HA, Lui JC, Kant SG, Oostdijk W, Gijsbers AC, Hoffer MJ, Karperien M, Walenkamp MJ, Noordam C, Voorhoeve PG, Mericq V, Pereira AM, Claahsen-van de Grinten HL, van Gool SA, Breuning MH, Losekoot M, Baron J, Ruivenkamp CA, Wit JM. van Duyvenvoorde HA, et al. Among authors: noordam c. Eur J Hum Genet. 2014 May;22(5):602-9. doi: 10.1038/ejhg.2013.203. Epub 2013 Sep 25. Eur J Hum Genet. 2014. PMID: 24065112 Free PMC article.
Inactivating PAPSS2 mutations in a patient with premature pubarche.
Noordam C, Dhir V, McNelis JC, Schlereth F, Hanley NA, Krone N, Smeitink JA, Smeets R, Sweep FC, Claahsen-van der Grinten HL, Arlt W. Noordam C, et al. N Engl J Med. 2009 May 28;360(22):2310-8. doi: 10.1056/NEJMoa0810489. N Engl J Med. 2009. PMID: 19474428 Free article.
24 results