Kannabiran C - Search Results

1

Genetic Markers for Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis in the Asian Indian Population: Implications on Prevention.

Shanbhag SS, Koduri MA, Kannabiran C, Donthineni PR, Singh V, Basu S. Shanbhag SS, et al. Among authors: kannabiran c. Front Genet. 2021 Jan 12;11:607532. doi: 10.3389/fgene.2020.607532. eCollection 2020. Front Genet. 2021. PMID: 33510770 Free PMC article. Review.

2

Trans-ethnic study confirmed independent associations of HLA-A*02:06 and HLA-B*44:03 with cold medicine-related Stevens-Johnson syndrome with severe ocular surface complications.

Ueta M, Kannabiran C, Wakamatsu TH, Kim MK, Yoon KC, Seo KY, Joo CK, Sangwan V, Rathi V, Basu S, Shamaila A, Lee HS, Yoon S, Sotozono C, Gomes JÁ, Tokunaga K, Kinoshita S. Ueta M, et al. Among authors: kannabiran c. Sci Rep. 2014 Aug 7;4:5981. doi: 10.1038/srep05981. Sci Rep. 2014. PMID: 25099678 Free PMC article.

3

IKZF1, a new susceptibility gene for cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis with severe mucosal involvement.

Ueta M, Sawai H, Sotozono C, Hitomi Y, Kaniwa N, Kim MK, Seo KY, Yoon KC, Joo CK, Kannabiran C, Wakamatsu TH, Sangwan V, Rathi V, Basu S, Ozeki T, Mushiroda T, Sugiyama E, Maekawa K, Nakamura R, Aihara M, Matsunaga K, Sekine A, Gomes JÁ, Hamuro J, Saito Y, Kubo M, Kinoshita S, Tokunaga K. Ueta M, et al. Among authors: kannabiran c. J Allergy Clin Immunol. 2015 Jun;135(6):1538-45.e17. doi: 10.1016/j.jaci.2014.12.1916. Epub 2015 Feb 8. J Allergy Clin Immunol. 2015. PMID: 25672763

4

Stevens-Johnson syndrome: The role of an ophthalmologist.

Jain R, Sharma N, Basu S, Iyer G, Ueta M, Sotozono C, Kannabiran C, Rathi VM, Gupta N, Kinoshita S, Gomes JA, Chodosh J, Sangwan VS. Jain R, et al. Among authors: kannabiran c. Surv Ophthalmol. 2016 Jul-Aug;61(4):369-99. doi: 10.1016/j.survophthal.2016.01.004. Epub 2016 Jan 30. Surv Ophthalmol. 2016. PMID: 26829569 Review.

5

Association of Human Leukocyte Antigen Class 1 genes with Stevens Johnson Syndrome with severe ocular complications in an Indian population.

Kannabiran C, Ueta M, Sangwan V, Rathi V, Basu S, Tokunaga K, Kinoshita S. Kannabiran C, et al. Sci Rep. 2017 Nov 21;7(1):15960. doi: 10.1038/s41598-017-15965-7. Sci Rep. 2017. PMID: 29162886 Free PMC article.

6

Genetics of Inherited Retinal Diseases in Understudied Populations.

Kannabiran C, Parameswarappa D, Jalali S. Kannabiran C, et al. Front Genet. 2022 Feb 28;13:858556. doi: 10.3389/fgene.2022.858556. eCollection 2022. Front Genet. 2022. PMID: 35295952 Free PMC article. Review.

7

Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy.

Salman M, Verma A, Chaurasia S, Prasad D, Kannabiran C, Singh V, Ramappa M. Salman M, et al. Among authors: kannabiran c. Orphanet J Rare Dis. 2022 Sep 17;17(1):361. doi: 10.1186/s13023-022-02521-4. Orphanet J Rare Dis. 2022. PMID: 36115991 Free PMC article.

8

Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy.

Salman M, Verma A, Chaurasia S, Prasad D, Kannabiran C, Singh V, Ramappa M. Salman M, et al. Among authors: kannabiran c. Orphanet J Rare Dis. 2023 Jun 29;18(1):170. doi: 10.1186/s13023-023-02791-6. Orphanet J Rare Dis. 2023. PMID: 37386499 Free PMC article. No abstract available.

9

Screening for homozygosity by descent in families with autosomal recessive retinitis pigmentosa.

Lalitha K, Jalali S, Kadakia T, Kannabiran C. Lalitha K, et al. Among authors: kannabiran c. J Genet. 2002 Aug;81(2):59-63. doi: 10.1007/BF02715901. J Genet. 2002. PMID: 12532037 Free article.

10

Genetics of corneal endothelial dystrophies.

Kannabiran C. Kannabiran C. J Genet. 2009 Dec;88(4):487-94. doi: 10.1007/s12041-009-0067-1. J Genet. 2009. PMID: 20090209 Free article. Review.

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