Aldave AJ - Search Results

1

Keratitis Fugax Hereditaria Associated With a Novel NLRP3 Mutation in a Non-Finnish Patient.

Jatavallabhula K, Onyia O, Chung DD, Williams D, Wang K, Aldave AJ. Jatavallabhula K, et al. Among authors: aldave aj. Cornea. 2024 Feb 1;43(2):253-256. doi: 10.1097/ICO.0000000000003399. Epub 2023 Oct 11. Cornea. 2024. PMID: 37823852

2

Central discoid corneal dystrophy.

Aldave AJ, Edward DP, Park AJ, Raber IM, Eagle RC Jr. Aldave AJ, et al. Cornea. 2002 Nov;21(8):739-44. doi: 10.1097/00003226-200211000-00001. Cornea. 2002. PMID: 12410027

3

Atypical vortex pattern of corneal deposits in granular corneal dystrophy.

Aldave AJ, Yellore VS, Hwang DG. Aldave AJ, et al. Cornea. 2003 Nov;22(8):754-9. doi: 10.1097/00003226-200311000-00008. Cornea. 2003. PMID: 14576527

4

Lattice dystrophy-like localized amyloidosis of the cornea secondary to trichiasis.

Aldave AJ, Principe AH, Lin DY, Yellore VS, Small KW. Aldave AJ, et al. Cornea. 2005 Jan;24(1):112-5. doi: 10.1097/01.ico.0000134194.71981.ab. Cornea. 2005. PMID: 15604878

5

Candidate gene screening for posterior polymorphous dystrophy.

Aldave AJ, Yellore VS, Principe AH, Abedi G, Merrill K, Chalukya M, Small KW, Udar N. Aldave AJ, et al. Cornea. 2005 Mar;24(2):151-5. doi: 10.1097/01.ico.0000141235.26096.1d. Cornea. 2005. PMID: 15725882

6

No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid deposition.

Aldave AJ, Rayner SA, King JA, Salem AK, Prechanond A, Hashida S, Affeldt JC, Meallet MA, Glasgow BJ, Small KW, Yellore VS. Aldave AJ, et al. Cornea. 2006 May;25(4):413-5. doi: 10.1097/01.ico.0000225260.41594.4a. Cornea. 2006. PMID: 16670477

7

Amniotic membrane transplantation with anterior stromal micropuncture for treatment of painful bullous keratopathy in eyes with poor visual potential.

Sonmez B, Kim BT, Aldave AJ. Sonmez B, et al. Among authors: aldave aj. Cornea. 2007 Feb;26(2):227-9. doi: 10.1097/01.ico.0000244876.92879.c1. Cornea. 2007. PMID: 17251820

8

Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.

Aldave AJ, Yellore VS, Bourla N, Momi RS, Khan MA, Salem AK, Rayner SA, Glasgow BJ, Kurtz I. Aldave AJ, et al. Cornea. 2007 Aug;26(7):896-900. doi: 10.1097/ICO.0b013e318074bb01. Cornea. 2007. PMID: 17667634

9

Keratoconus is not associated with mutations in COL8A1 and COL8A2.

Aldave AJ, Bourla N, Yellore VS, Rayner SA, Khan MA, Salem AK, Sonmez B. Aldave AJ, et al. Cornea. 2007 Sep;26(8):963-5. doi: 10.1097/ICO.0b013e31811dfaf7. Cornea. 2007. PMID: 17721297

10

Classic lattice corneal dystrophy associated with monoclonal gammopathy after exclusion of a TGFBI mutation.

Kamal KM, Rayner SA, Chen MC, Aldave AJ. Kamal KM, et al. Among authors: aldave aj. Cornea. 2009 Jan;28(1):97-8. doi: 10.1097/ICO.0b013e31818200f4. Cornea. 2009. PMID: 19092416 Free PMC article.

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