Reddy AB - Search Results

1

Identification of R368H as a predominant CYP1B1 allele causing primary congenital glaucoma in Indian patients.

Reddy AB, Panicker SG, Mandal AK, Hasnain SE, Balasubramanian D. Reddy AB, et al. Invest Ophthalmol Vis Sci. 2003 Oct;44(10):4200-3. doi: 10.1167/iovs.02-0945. Invest Ophthalmol Vis Sci. 2003. PMID: 14507861

2

Myocilin gene implicated in primary congenital glaucoma.

Kaur K, Reddy AB, Mukhopadhyay A, Mandal AK, Hasnain SE, Ray K, Thomas R, Balasubramanian D, Chakrabarti S. Kaur K, et al. Among authors: reddy ab. Clin Genet. 2005 Apr;67(4):335-40. doi: 10.1111/j.1399-0004.2005.00411.x. Clin Genet. 2005. PMID: 15733270

3

Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees.

Panicker SG, Reddy AB, Mandal AK, Ahmed N, Nagarajaram HA, Hasnain SE, Balasubramanian D. Panicker SG, et al. Among authors: reddy ab. Invest Ophthalmol Vis Sci. 2002 May;43(5):1358-66. Invest Ophthalmol Vis Sci. 2002. PMID: 11980847

4

Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly.

Panicker SG, Sampath S, Mandal AK, Reddy AB, Ahmed N, Hasnain SE. Panicker SG, et al. Among authors: reddy ab. Invest Ophthalmol Vis Sci. 2002 Dec;43(12):3613-6. Invest Ophthalmol Vis Sci. 2002. PMID: 12454026

5

Congenital glaucoma associated with 22p+ variant in a dysmorphic child.

Mandal AK, Prabhakara K, Reddy AB, Devi AR, Panicker SG. Mandal AK, et al. Among authors: reddy ab. Indian J Ophthalmol. 2003 Dec;51(4):355-7. Indian J Ophthalmol. 2003. PMID: 14750628 Free article.

6

Correlations of genotype with phenotype in Indian patients with primary congenital glaucoma.

Panicker SG, Mandal AK, Reddy AB, Gothwal VK, Hasnain SE. Panicker SG, et al. Among authors: reddy ab. Invest Ophthalmol Vis Sci. 2004 Apr;45(4):1149-56. doi: 10.1167/iovs.03-0404. Invest Ophthalmol Vis Sci. 2004. PMID: 15037581

7

Disease-causing mutations in proteins: structural analysis of the CYP1B1 mutations causing primary congenital glaucoma in humans.

Achary MS, Reddy AB, Chakrabarti S, Panicker SG, Mandal AK, Ahmed N, Balasubramanian D, Hasnain SE, Nagarajaram HA. Achary MS, et al. Among authors: reddy ab. Biophys J. 2006 Dec 15;91(12):4329-39. doi: 10.1529/biophysj.106.085498. Epub 2006 Sep 8. Biophys J. 2006. PMID: 16963504 Free PMC article.

8

PAX6 gene mutations and genotype-phenotype correlations in sporadic cases of aniridia from India.

Dharmaraj N, Reddy A, Kiran V, Mandal A, Panicker S, Chakrabarti S. Dharmaraj N, et al. Ophthalmic Genet. 2003 Sep;24(3):161-5. doi: 10.1076/opge.24.3.161.15607. Ophthalmic Genet. 2003. PMID: 12868034

9

Schizencephaly Associated With Bipolar Affective Disorder.

Rama Rao R, Reddy ABS, P D, Koul A. Rama Rao R, et al. Among authors: reddy abs. Cureus. 2024 Feb 20;16(2):e54534. doi: 10.7759/cureus.54534. eCollection 2024 Feb. Cureus. 2024. PMID: 38516433 Free PMC article.

10

Infrared thermal images using PCSAN-Net-DBOA: An approach of breast cancer classification.

Vijayarajan SM, Manoj Kumar D, Sudha G, Reddy AB. Vijayarajan SM, et al. Among authors: reddy ab. Microsc Res Tech. 2024 Mar 19. doi: 10.1002/jemt.24550. Online ahead of print. Microsc Res Tech. 2024. PMID: 38501825

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