Drop SLS - Search Results

1

Update on the predictability of tall stature from DNA markers in Europeans.

Liu F, Zhong K, Jing X, Uitterlinden AG, Hendriks AEJ, Drop SLS, Kayser M. Liu F, et al. Among authors: drop sls. Forensic Sci Int Genet. 2019 Sep;42:8-13. doi: 10.1016/j.fsigen.2019.05.006. Epub 2019 Jun 1. Forensic Sci Int Genet. 2019. PMID: 31207428 Free article.

2

Common DNA variants predict tall stature in Europeans.

Liu F, Hendriks AE, Ralf A, Boot AM, Benyi E, Sävendahl L, Oostra BA, van Duijn C, Hofman A, Rivadeneira F, Uitterlinden AG, Drop SL, Kayser M. Liu F, et al. Hum Genet. 2014 May;133(5):587-97. doi: 10.1007/s00439-013-1394-0. Epub 2013 Nov 20. Hum Genet. 2014. PMID: 24253421

3

Computer-aided skeletal age scores in healthy children, girls with Turner syndrome, and in children with constitutionally tall stature.

Van Teunenbroek A, De Waal W, Roks A, Chinafo P, Fokker M, Mulder P, De Muinck Keizer-Schrama S, Drop S. Van Teunenbroek A, et al. Pediatr Res. 1996 Feb;39(2):360-7. doi: 10.1203/00006450-199602000-00028. Pediatr Res. 1996. PMID: 8825813

4

Radiographic absorptiometry of the phalanges in healthy children and in girls with Turner syndrome.

van Teunenbroek A, Mulder P, de Muinck Keizer-Schrama S, van Kuijk C, Grashuis J, van Bodegom JW, Drop S. van Teunenbroek A, et al. Bone. 1995 Jul;17(1):71-8. doi: 10.1016/8756-3282(95)00139-5. Bone. 1995. PMID: 7577161

5

Validation of a calibrated prediction model for response to growth hormone treatment in an independent cohort.

de Ridder MA, Stijnen T, Drop SL, Blum WF, Hokken-Koelega AC. de Ridder MA, et al. Horm Res. 2006;66(1):13-6. doi: 10.1159/000093047. Epub 2006 May 2. Horm Res. 2006. PMID: 16675910

6

Isolated 17,20-lyase deficiency due to the cytochrome b5 mutation W27X.

Kok RC, Timmerman MA, Wolffenbuttel KP, Drop SL, de Jong FH. Kok RC, et al. J Clin Endocrinol Metab. 2010 Mar;95(3):994-9. doi: 10.1210/jc.2008-1745. Epub 2010 Jan 15. J Clin Endocrinol Metab. 2010. PMID: 20080843

7

Longitudinal follow-up of bone density and body composition in children with precocious or early puberty before, during and after cessation of GnRH agonist therapy.

van der Sluis IM, Boot AM, Krenning EP, Drop SL, de Muinck Keizer-Schrama SM. van der Sluis IM, et al. J Clin Endocrinol Metab. 2002 Feb;87(2):506-12. doi: 10.1210/jcem.87.2.8202. J Clin Endocrinol Metab. 2002. PMID: 11836277 Free article. Clinical Trial.

8

Mutation analysis of the LH receptor gene in Leydig cell adenoma and hyperplasia and functional and biochemical studies of activating mutations of the LH receptor gene.

Boot AM, Lumbroso S, Verhoef-Post M, Richter-Unruh A, Looijenga LH, Funaro A, Beishuizen A, van Marle A, Drop SL, Themmen AP. Boot AM, et al. J Clin Endocrinol Metab. 2011 Jul;96(7):E1197-205. doi: 10.1210/jc.2010-3031. Epub 2011 Apr 13. J Clin Endocrinol Metab. 2011. PMID: 21490077 Free PMC article.

9

A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses.

van der Eerden BC, van der Heyden JC, van Hamburg JP, Schreuders-Koedam M, Asmawidjaja PS, de Muinck Keizer-Schrama SM, Boot AM, Lubberts E, Drop SL, van Leeuwen JP. van der Eerden BC, et al. Bone. 2014 Dec;69:6-11. doi: 10.1016/j.bone.2014.08.005. Epub 2014 Sep 6. Bone. 2014. PMID: 25201466

10

Multilingual Global E-Learning Pediatric Endocrinology and Diabetes Curriculum for Front Line Health Care Providers in Resource-Limited Countries: Development Study.

Kalaitzoglou E, Majaliwa E, Zacharin M, de Beaufort C, Chanoine JP, van Wijngaard-DeVugt C, Sperla E, Boot AM, Drop SLS. Kalaitzoglou E, et al. Among authors: drop sls. JMIR Form Res. 2020 Nov 5;4(11):e18555. doi: 10.2196/18555. JMIR Form Res. 2020. PMID: 33151156 Free PMC article.

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