de Graaff LCG - Search Results

1

Transition readiness among adolescents with rare endocrine conditions.

van Alewijk L, Davidse K, Pellikaan K, van Eck J, Hokken-Koelega ACS, Sas TCJ, Hannema S, van der Lely AJ, de Graaff LCG. van Alewijk L, et al. Among authors: de graaff lcg. Endocr Connect. 2021 Apr 22;10(4):432-446. doi: 10.1530/EC-20-0304. Endocr Connect. 2021. PMID: 33764888 Free PMC article.

2

Body proportions before and during growth hormone therapy in children with chronic renal failure.

de Graaff LC, Mulder PG, Hokken-Koelega AC. de Graaff LC, et al. Pediatr Nephrol. 2003 Jul;18(7):679-84. doi: 10.1007/s00467-003-1090-8. Epub 2003 May 7. Pediatr Nephrol. 2003. PMID: 12734746 Clinical Trial.

3

GH receptor d3 polymorphism in Dutch patients with MPHD and IGHD born small or appropriate for gestational age.

de Graaff LC, Meyer S, Els C, Hokken-Koelega AC. de Graaff LC, et al. Clin Endocrinol (Oxf). 2008 Jun;68(6):930-4. doi: 10.1111/j.1365-2265.2007.03140.x. Epub 2007 Nov 19. Clin Endocrinol (Oxf). 2008. PMID: 18031312

4

Facial and pituitary morphology are related in Dutch patients with GH deficiency.

de Graaff LC, Baan J, Govaerts LC, Hokken-Koelega AC. de Graaff LC, et al. Clin Endocrinol (Oxf). 2008 Jul;69(1):112-6. doi: 10.1111/j.1365-2265.2007.03167.x. Epub 2008 Jul 1. Clin Endocrinol (Oxf). 2008. PMID: 18182094

5

Genetic screening of a Dutch population with isolated GH deficiency (IGHD).

de Graaff LC, Argente J, Veenma DC, Herrebout MA, Friesema EC, Uitterlinden AG, Drent ML, Campos-Barros A, Hokken-Koelega AC. de Graaff LC, et al. Clin Endocrinol (Oxf). 2009 May;70(5):742-50. doi: 10.1111/j.1365-2265.2008.03414.x. Epub 2008 Sep 10. Clin Endocrinol (Oxf). 2009. PMID: 18785993

6

Antipituitary antibodies in dutch patients with idiopathic hypopituitarism.

de Graaff LC, De Bellis A, Bellastella A, Hokken-Koelega AC. de Graaff LC, et al. Horm Res. 2009 Jan;71(1):22-7. doi: 10.1159/000173738. Epub 2008 Nov 27. Horm Res. 2009. PMID: 19039233

7

Genetic polymorphisms in the locus control region and promoter of GH1 are related to serum IGF-I levels and height in patients with isolated growth hormone deficiency and healthy controls.

de Graaff LC, Argente J, van Meurs JB, Uitterlinden AG, Hokken-Koelega AC. de Graaff LC, et al. Horm Res Paediatr. 2010;73(1):25-34. doi: 10.1159/000271913. Epub 2010 Jan 15. Horm Res Paediatr. 2010. PMID: 20190537

8

PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency.

de Graaff LC, Argente J, Veenma DC, Drent ML, Uitterlinden AG, Hokken-Koelega AC. de Graaff LC, et al. Horm Res Paediatr. 2010;73(5):363-71. doi: 10.1159/000308169. Epub 2010 Apr 14. Horm Res Paediatr. 2010. PMID: 20389107

9

Isolated GH deficiency: mutation screening and copy number analysis of HMGA2 and CDK6 genes.

Gorbenko del Blanco D, de Graaff LC, Posthouwer D, Visser TJ, Hokken-Koelega AC. Gorbenko del Blanco D, et al. Eur J Endocrinol. 2011 Oct;165(4):537-44. doi: 10.1530/EJE-11-0478. Epub 2011 Jul 29. Eur J Endocrinol. 2011. PMID: 21803798

10

Growth hormone insensitivity syndrome caused by a heterozygous GHR mutation: phenotypic variability owing to moderation by nonsense-mediated decay.

Gorbenko del Blanco D, de Graaff LC, Visser TJ, Hokken-Koelega AC. Gorbenko del Blanco D, et al. Clin Endocrinol (Oxf). 2012 May;76(5):706-12. doi: 10.1111/j.1365-2265.2011.04304.x. Clin Endocrinol (Oxf). 2012. PMID: 22117696

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