Dhiman V - Search Results

1

HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA: A NOVEL HOMOZYGOUS MUTATION IN SLC34A3 AND LITERATURE REVIEW.

Bhadada SK, Sridhar S, Dhiman V, Wong K, Bennetts B, Naot D, Jayaraman S, Cundy T. Bhadada SK, et al. Among authors: dhiman v. AACE Clin Case Rep. 2020 May 11;6(3):e105-e112. doi: 10.4158/ACCR-2019-0456. eCollection 2020 May-Jun. AACE Clin Case Rep. 2020. PMID: 32524022 Free PMC article.

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: dhiman v. 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: dhiman v. 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

Predictors of atypical femoral fractures during long term bisphosphonate therapy: a case series & review of literature.

Bhadada SK, Sridhar S, Muthukrishnan J, Mithal A, Sharma DC, Bhansali A, Dhiman V. Bhadada SK, et al. Among authors: dhiman v. Indian J Med Res. 2014 Jul;140(1):46-54. Indian J Med Res. 2014. PMID: 25222777 Free PMC article. Review.

5

VISUAL VIGNETTE.

Dhiman V, Bhadada SK, Dhanwada S, Gopinathan NR. Dhiman V, et al. Endocr Pract. 2019 Feb;25(2):202. doi: 10.4158/EP-2018-0278. Epub 2018 Jul 23. Endocr Pract. 2019. PMID: 30035622 No abstract available.

6

Fibrogenesis Imperfecta Ossium: Clinical Approach to Diagnosis and Management of a Rare Skeletal Disorder.

Dhaliwal R, Dhiman V, Rao SD, Bhadada SK. Dhaliwal R, et al. Among authors: dhiman v. J Clin Endocrinol Metab. 2019 Sep 1;104(9):4005-4015. doi: 10.1210/jc.2018-01180. J Clin Endocrinol Metab. 2019. PMID: 30869792

7

Fibrogenesis Imperfecta Ossium.

Bhadada SK, Dhaliwal R, Dhiman V, Rao SD. Bhadada SK, et al. Among authors: dhiman v. Calcif Tissue Int. 2019 May;104(5):561-569. doi: 10.1007/s00223-019-00547-8. Epub 2019 May 8. Calcif Tissue Int. 2019. PMID: 31069441 Review.

8

Co-administration of Systemic and Intralesional Zoledronic Acid in a Case of Fibrous Dysplasia: A Potentially Novel Therapy.

Bhadada SK, Pal R, Sood A, Dhiman V, Saini UC. Bhadada SK, et al. Among authors: dhiman v. Front Endocrinol (Lausanne). 2019 Nov 19;10:803. doi: 10.3389/fendo.2019.00803. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31803145 Free PMC article.

9

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: dhiman v. 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.

10

Adult hypophosphatasia with a novel ALPL mutation: Report of an Indian kindred.

Bhadada SK, Pal R, Dhiman V, Alonso N, Ralston SH, Kaur S, Gupta R. Bhadada SK, et al. Among authors: dhiman v. Bone Rep. 2020 Jan 24;12:100247. doi: 10.1016/j.bonr.2020.100247. eCollection 2020 Jun. Bone Rep. 2020. PMID: 32025537 Free PMC article.

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