Damji KF - Search Results

1

Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American families.

Allingham RR, Wiggs JL, Damji KF, Herndon L, Youn J, Tallett DA, Jones KH, Del Bono EA, Reardon M, Haines JL, Pericak-Vance MA. Allingham RR, et al. Among authors: damji kf. Hum Hered. 1998 Sep-Oct;48(5):251-5. doi: 10.1159/000022812. Hum Hered. 1998. PMID: 9748694

2

The distinction between juvenile and adult-onset primary open-angle glaucoma.

Wiggs JL, Damji KF, Haines JL, Pericak-Vance MA, Allingham RR. Wiggs JL, et al. Among authors: damji kf. Am J Hum Genet. 1996 Jan;58(1):243-4. Am J Hum Genet. 1996. PMID: 8554064 Free PMC article. No abstract available.

3

Linkage of a gene for macular corneal dystrophy to chromosome 16.

Vance JM, Jonasson F, Lennon F, Sarrica J, Damji KF, Stauffer J, Pericak-Vance MA, Klintworth GK. Vance JM, et al. Among authors: damji kf. Am J Hum Genet. 1996 Apr;58(4):757-62. Am J Hum Genet. 1996. PMID: 8644739 Free PMC article.

4

Efficacy of autologous blood injection for treating overfiltering or leaking blebs after glaucoma surgery.

Choudhri SA, Herndon LW, Damji KF, Allingham RR, Shields MB. Choudhri SA, et al. Among authors: damji kf. Am J Ophthalmol. 1997 Apr;123(4):554-5. doi: 10.1016/s0002-9394(14)70186-2. Am J Ophthalmol. 1997. PMID: 9124257

5

Central corneal thickness in normal, glaucomatous, and ocular hypertensive eyes.

Herndon LW, Choudhri SA, Cox T, Damji KF, Shields MB, Allingham RR. Herndon LW, et al. Among authors: damji kf. Arch Ophthalmol. 1997 Sep;115(9):1137-41. doi: 10.1001/archopht.1997.01100160307007. Arch Ophthalmol. 1997. PMID: 9298054 Clinical Trial.

6

Pseudoexfoliation syndrome in Icelandic families.

Allingham RR, Loftsdottir M, Gottfredsdottir MS, Thorgeirsson E, Jonasson F, Sverisson T, Hodge WG, Damji KF, Stefánsson E. Allingham RR, et al. Among authors: damji kf. Br J Ophthalmol. 2001 Jun;85(6):702-7. doi: 10.1136/bjo.85.6.702. Br J Ophthalmol. 2001. PMID: 11371492 Free PMC article.

7

Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.

Damji KF, Allingham RR, Pollock SC, Small K, Lewis KE, Stajich JM, Yamaoka LH, Vance JM, Pericak-Vance MA. Damji KF, et al. Arch Neurol. 1996 Apr;53(4):338-44. doi: 10.1001/archneur.1996.00550040074016. Arch Neurol. 1996. PMID: 8929156 Review.

8

Molecular genetics is revolutionizing our understanding of ophthalmic disease.

Damji KF, Allingham RR. Damji KF, et al. Am J Ophthalmol. 1997 Oct;124(4):530-43. doi: 10.1016/s0002-9394(14)70869-4. Am J Ophthalmol. 1997. PMID: 9323944 Review.

9

Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant disease.

Damji KF, Gallione CJ, Allingham RR, Slotterbeck B, Guttmacher AE, Pasyk KA, Vance JM, Pericak-Vance MA, Speer MC, Marchuk DA. Damji KF, et al. Hum Genet. 1998 Feb;102(2):207-12. doi: 10.1007/s004390050679. Hum Genet. 1998. PMID: 9521591 Free article.

10

Decrease in intraocular pressure after orbital decompression for thyroid orbitopathy.

Dev S, Damji KF, DeBacker CM, Cox TA, Dutton JJ, Allingham RR. Dev S, et al. Among authors: damji kf. Can J Ophthalmol. 1998 Oct;33(6):314-9. Can J Ophthalmol. 1998. PMID: 9818128

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

153 results

Search Page

Filters