Selina A - Search Results

1

Case report of a PRDM5 linked brittle cornea syndrome type 2 in association with a novel SLC6A5 mutation.

Selina A, John D, Loganathan L, Madhuri V. Selina A, et al. Indian J Ophthalmol. 2020 Nov;68(11):2545-2547. doi: 10.4103/ijo.IJO_325_20. Indian J Ophthalmol. 2020. PMID: 33120686 Free PMC article.

2

MATN3 Mutation Causing Spondyloepimetaphyseal Dysplasia.

Shyamasundar LG, Loganathan L, Kumar A, Selina A, Madhuri V. Shyamasundar LG, et al. Among authors: selina a. Indian J Pediatr. 2020 Mar;87(3):227-228. doi: 10.1007/s12098-019-03100-5. Epub 2019 Nov 14. Indian J Pediatr. 2020. PMID: 31724101 No abstract available.

3

Osteogenesis imperfecta: Novel genetic variants and clinical observations from a clinical exome study of 54 Indian patients.

Madhuri V, Selina A, Loganathan L, Kumar A, Kumar V, Raymond R, Ramesh S, Vincy N, Joel G, James D, Kandagaddala M, B A. Madhuri V, et al. Among authors: selina a. Ann Hum Genet. 2021 Jan;85(1):37-46. doi: 10.1111/ahg.12403. Epub 2020 Aug 7. Ann Hum Genet. 2021. PMID: 32770541

4

A Recurrent Biallelic Pathogenic Variant in TBXAS1 Gene Causing Ghosal Hematodiaphyseal Dysplasia.

Selina A, Kandagaddala M, Madhuri V. Selina A, et al. Indian J Pediatr. 2021 Apr;88(4):381-382. doi: 10.1007/s12098-020-03581-9. Epub 2020 Nov 27. Indian J Pediatr. 2021. PMID: 33244729 No abstract available.

5

Novel TRPV4 Pathogenic Variant in Severe Metatropic Skeletal Dysplasia: A Case Report.

James D, Subramanian L, Selina A, Palocaren T, Madhuri V. James D, et al. Among authors: selina a. Malays Orthop J. 2022 Jul;16(2):145-149. doi: 10.5704/MOJ.2207.021. Malays Orthop J. 2022. PMID: 35992980 Free PMC article.

6

A Novel Biallelic Splice Site Variant in the SPARC Gene Causing Severe Osteogenesis Imperfecta.

Selina A, James D, Madhuri V. Selina A, et al. Indian J Pediatr. 2023 Jun;90(6):626. doi: 10.1007/s12098-023-04541-9. Epub 2023 Mar 30. Indian J Pediatr. 2023. PMID: 36995644 No abstract available.

7

SERPINF1 gene variants causing late-onset progressive deforming osteogenesis imperfecta - A study of 18 patients from India.

Selina A, Kandagaddala M, Kumar V, Abraham SSC, Danda S, Madhuri V. Selina A, et al. Bone Rep. 2023 May 26;18:101690. doi: 10.1016/j.bonr.2023.101690. eCollection 2023 Jun. Bone Rep. 2023. PMID: 37425194 Free PMC article.

8

Perthes-Like Disorder in a Child with Atypical Bohring-Opitz Syndrome.

Altaf MT, Kandagaddala M, Selina A, Madhuri V. Altaf MT, et al. Among authors: selina a. JBJS Case Connect. 2024 Jan 5;14(1). doi: 10.2106/JBJS.CC.23.00433. eCollection 2024 Jan 1. JBJS Case Connect. 2024. PMID: 38181165

9

Pamidronate Response in a Novel Biallelic CREB3L1 Gene Mutation-Associated Osteogenesis Imperfecta: A Case Report.

Selina A, Kandagaddala M, Madhuri V. Selina A, et al. JBJS Case Connect. 2024 Jul 26;14(3). doi: 10.2106/JBJS.CC.24.00093. eCollection 2024 Jul 1. JBJS Case Connect. 2024. PMID: 39058796

10

The relationship between estrogen receptors and microtubule dynamics in post-menopausal rat brain.

Selina AK, Murat K, Emre K, Ismail M, Bunyami U, Cemal G. Selina AK, et al. Acta Histochem. 2015 Oct;117(8):747-51. doi: 10.1016/j.acthis.2015.08.005. Epub 2015 Aug 28. Acta Histochem. 2015. PMID: 26319549

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