de Bruin C - Search Results

1

Somatic growth in single ventricle patients: A systematic review and meta-analysis.

Van den Eynde J, Bartelse S, Rijnberg FM, Kutty S, Jongbloed MRM, de Bruin C, Hazekamp MG, Le Cessie S, Roest AAW. Van den Eynde J, et al. Among authors: de bruin c. Acta Paediatr. 2023 Feb;112(2):186-199. doi: 10.1111/apa.16562. Epub 2022 Oct 17. Acta Paediatr. 2023. PMID: 36200280 Free PMC article. Review.

2

Fetal growth restriction inhibits childhood growth despite catch-up in discordant identical twins: an observational cohort study.

Groene SG, Gremmen IJ, van Zwet EW, Roest AAW, Haak MC, van Klink JMM, Lopriore E, Heijmans BT, de Bruin C. Groene SG, et al. Among authors: de bruin c. Eur J Endocrinol. 2023 Aug 2;189(2):183-189. doi: 10.1093/ejendo/lvad103. Eur J Endocrinol. 2023. PMID: 37548178

3

Differential Diagnosis of the Short IGF-I-Deficient Child with Apparently Normal Growth Hormone Secretion.

Wit JM, Joustra SD, Losekoot M, van Duyvenvoorde HA, de Bruin C. Wit JM, et al. Among authors: de bruin c. Horm Res Paediatr. 2021;94(3-4):81-104. doi: 10.1159/000516407. Epub 2021 Jun 4. Horm Res Paediatr. 2021. PMID: 34091447 Free article. Review.

4

Ways to Improve the Diagnosis of Growth Hormone Deficiency.

Wit JM, Vliegenthart J, Joustra SD, de Bruin C, Bakker B, van der Kaay DCM, Bocca G. Wit JM, et al. Among authors: de bruin c. Horm Res Paediatr. 2022;95(1):93-96. doi: 10.1159/000522541. Epub 2022 Feb 10. Horm Res Paediatr. 2022. PMID: 35144257 Free article. No abstract available.

5

An XRCC4 splice mutation associated with severe short stature, gonadal failure, and early-onset metabolic syndrome.

de Bruin C, Mericq V, Andrew SF, van Duyvenvoorde HA, Verkaik NS, Losekoot M, Porollo A, Garcia H, Kuang Y, Hanson D, Clayton P, van Gent DC, Wit JM, Hwa V, Dauber A. de Bruin C, et al. J Clin Endocrinol Metab. 2015 May;100(5):E789-98. doi: 10.1210/jc.2015-1098. Epub 2015 Mar 5. J Clin Endocrinol Metab. 2015. PMID: 25742519 Free PMC article.

6

Children Born Small for Gestational Age: Differential Diagnosis, Molecular Genetic Evaluation, and Implications.

Finken MJJ, van der Steen M, Smeets CCJ, Walenkamp MJE, de Bruin C, Hokken-Koelega ACS, Wit JM. Finken MJJ, et al. Among authors: de bruin c. Endocr Rev. 2018 Dec 1;39(6):851-894. doi: 10.1210/er.2018-00083. Endocr Rev. 2018. PMID: 29982551 Review.

7

TGDS pathogenic variants cause Catel-Manzke syndrome without hyperphalangy.

Boschann F, Stuurman KE, de Bruin C, van Slegtenhorst M, van Duyvenvoorde HA, Kant SG, Ehmke N. Boschann F, et al. Among authors: de bruin c. Am J Med Genet A. 2020 Mar;182(3):431-436. doi: 10.1002/ajmg.a.61419. Epub 2019 Nov 25. Am J Med Genet A. 2020. PMID: 31769200

8

A Proposal for the Interpretation of Serum IGF-I Concentration as Part of Laboratory Screening in Children with Growth Failure.

Wit JM, Bidlingmaier M, de Bruin C, Oostdijk W. Wit JM, et al. Among authors: de bruin c. J Clin Res Pediatr Endocrinol. 2020 Jun 3;12(2):130-139. doi: 10.4274/jcrpe.galenos.2019.2019.0176. Epub 2019 Dec 17. J Clin Res Pediatr Endocrinol. 2020. PMID: 31842524 Free PMC article. Review.

9

Novel Clinical Criteria Allow Detection of Short Stature Homeobox-Containing Gene Haploinsufficiency Caused by Either Gene or Enhancer Region Defects.

Joustra SD, Kamp GA, Stalman SE, Donze SH, Losekoot M, Kant SG, de Bruin C, Oostdijk W, Wit JM. Joustra SD, et al. Among authors: de bruin c. Horm Res Paediatr. 2019;92(6):372-381. doi: 10.1159/000507215. Epub 2020 Apr 28. Horm Res Paediatr. 2019. PMID: 32344414 Free article. Clinical Trial.

10

Anthropometric, biochemical and hormonal profiles of the partially admixed pygmoid group in Rampasasa (Flores, Indonesia).

Pulungan A, Andarie AA, Soesanti F, Yassien MR, de Bruin C, Wijaya A, Firmansyah A, Wit JM. Pulungan A, et al. Among authors: de bruin c. J Pediatr Endocrinol Metab. 2021 Apr 13;34(5):547-557. doi: 10.1515/jpem-2020-0526. Print 2021 May 26. J Pediatr Endocrinol Metab. 2021. PMID: 33851527

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