Van Hul W - Search Results

1

Fibrogenesis Imperfecta Ossium and Response to Human Growth Hormone: A Potential Therapy.

Bhadada SK, Dhiman V, Mukherjee S, Aggarwal S, Bal A, Sukumar SP, Sood A, Sharma DC, Khandelwal N, Bhansali A, Van Hul W, Rao SD. Bhadada SK, et al. Among authors: van hul w. J Clin Endocrinol Metab. 2017 May 1;102(5):1750-1756. doi: 10.1210/jc.2016-3055. J Clin Endocrinol Metab. 2017. PMID: 28323922

2

Novel SOST gene mutation in a sclerosteosis patient and her parents.

Bhadada SK, Rastogi A, Steenackers E, Boudin E, Arya A, Dhiman V, Bhansali A, Van Hul W. Bhadada SK, et al. Among authors: van hul w. Bone. 2013 Feb;52(2):707-10. doi: 10.1016/j.bone.2012.10.009. Epub 2012 Oct 16. Bone. 2013. PMID: 23079137

3

Camurati-Engelmann disease (progressive diaphyseal dysplasia): reports of an Indian kindred.

Bhadada SK, Sridhar S, Steenackers E, Dhiman V, Mortier G, Bhansali A, Van Hul W. Bhadada SK, et al. Among authors: van hul w. Calcif Tissue Int. 2014 Feb;94(2):240-7. doi: 10.1007/s00223-013-9804-9. Epub 2013 Oct 24. Calcif Tissue Int. 2014. PMID: 24154985

4

Sclerosing bone dysplasias.

Boudin E, Van Hul W. Boudin E, et al. Among authors: van hul w. Best Pract Res Clin Endocrinol Metab. 2018 Oct;32(5):707-723. doi: 10.1016/j.beem.2018.06.003. Epub 2018 Jun 18. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 30449550 Review.

5

Spondylo-epi-metaphyseal dysplasia due to a homozygous missense mutation in the gene encoding Matrilin-3 (T120M).

Das L, Dhiman V, Van Hul W, Bhansali A, Gogate Y, Steenackers E, Mortier G, Bhadada SK. Das L, et al. Among authors: van hul w. Bone Rep. 2020 Jan 11;12:100245. doi: 10.1016/j.bonr.2020.100245. eCollection 2020 Jun. Bone Rep. 2020. PMID: 32025536 Free PMC article.

6

Camurati-Engelmann Disease Complicated by Hypopituitarism: Management Challenges and Literature Review of Outcomes With Bisphosphonates.

Das L, Dhiman V, Dutta P, Sood A, Prakash M, Kaur S, Steenackers E, Hendrickx G, Dayal D, Van Hul W, Bhadada SK. Das L, et al. Among authors: van hul w. AACE Clin Case Rep. 2021 Oct 20;8(2):58-64. doi: 10.1016/j.aace.2021.10.002. eCollection 2022 Mar-Apr. AACE Clin Case Rep. 2021. PMID: 35415221 Free PMC article.

7

The genetics of low-density lipoprotein receptor-related protein 5 in bone: a story of extremes.

Balemans W, Van Hul W. Balemans W, et al. Among authors: van hul w. Endocrinology. 2007 Jun;148(6):2622-9. doi: 10.1210/en.2006-1352. Epub 2007 Mar 29. Endocrinology. 2007. PMID: 17395706 Review.

8

WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders.

Huybrechts Y, Mortier G, Boudin E, Van Hul W. Huybrechts Y, et al. Among authors: van hul w. Front Endocrinol (Lausanne). 2020 Apr 9;11:165. doi: 10.3389/fendo.2020.00165. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32328030 Free PMC article. Review.

9

DNA Methylation Profiling and Genomic Analysis in 20 Children with Short Stature Who Were Born Small for Gestational Age.

Peeters S, Declerck K, Thomas M, Boudin E, Beckers D, Chivu O, Heinrichs C, Devriendt K, de Zegher F, Van Hul W, Vanden Berghe W, De Schepper J, Rooman R, Mortier G; WES-BESPEED Study Group. Peeters S, et al. Among authors: van hul w. J Clin Endocrinol Metab. 2020 Dec 1;105(12):dgaa465. doi: 10.1210/clinem/dgaa465. J Clin Endocrinol Metab. 2020. PMID: 32685970

10

Editorial: Innovative Therapies in Bone Biology: What Can Be Learned From Rare Bone Diseases?

Eekhoff EMW, de Vries TJ, Sakkers RJB, Van Hul W. Eekhoff EMW, et al. Among authors: van hul w. Front Endocrinol (Lausanne). 2022 Jun 9;13:928667. doi: 10.3389/fendo.2022.928667. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35757420 Free PMC article. No abstract available.

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