PubMed (OMIM) for id: 343836

Year	Number of Results
1961	1
1964	1
1968	1
1969	2
1977	2
1995	2
2001	1
2002	1
2005	1
2024	0

1

Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.

Krafchak CM, Pawar H, Moroi SE, Sugar A, Lichter PR, Mackey DA, Mian S, Nairus T, Elner V, Schteingart MT, Downs CA, Kijek TG, Johnson JM, Trager EH, Rozsa FW, Mandal MN, Epstein MP, Vollrath D, Ayyagari R, Boehnke M, Richards JE. Krafchak CM, et al. Am J Hum Genet. 2005 Nov;77(5):694-708. doi: 10.1086/497348. Epub 2005 Sep 14. Am J Hum Genet. 2005. PMID: 16252232 Free PMC article.

2

POSTERIOR POLYMORPHOUS DEGENERATION OF THE CORNEA.

BERGMAN GD. BERGMAN GD. Am J Ophthalmol. 1964 Jul;58:125-8. doi: 10.1016/0002-9394(64)90601-4. Am J Ophthalmol. 1964. PMID: 14177965 No abstract available.

3

Hereditary nonprogressive deep corneal dystrophy.

KWEDAR EW. KWEDAR EW. Arch Ophthalmol. 1961 Jan;65:127-9. doi: 10.1001/archopht.1961.01840020129021. Arch Ophthalmol. 1961. PMID: 13755549 No abstract available.

4

VSX1: a gene for posterior polymorphous dystrophy and keratoconus.

Héon E, Greenberg A, Kopp KK, Rootman D, Vincent AL, Billingsley G, Priston M, Dorval KM, Chow RL, McInnes RR, Heathcote G, Westall C, Sutphin JE, Semina E, Bremner R, Stone EM. Héon E, et al. Hum Mol Genet. 2002 May 1;11(9):1029-36. doi: 10.1093/hmg/11.9.1029. Hum Mol Genet. 2002. PMID: 11978762

5

Posterior polymorphous membranous dystrophy with overlapping features of iridocorneal endothelial syndrome.

Anderson NJ, Badawi DY, Grossniklaus HE, Stulting RD. Anderson NJ, et al. Arch Ophthalmol. 2001 Apr;119(4):624-5. doi: 10.1001/archopht.119.4.624. Arch Ophthalmol. 2001. PMID: 11296040 No abstract available.

6

Linkage of congenital hereditary endothelial dystrophy to chromosome 20.

Toma NM, Ebenezer ND, Inglehearn CF, Plant C, Ficker LA, Bhattacharya SS. Toma NM, et al. Hum Mol Genet. 1995 Dec;4(12):2395-8. doi: 10.1093/hmg/4.12.2395. Hum Mol Genet. 1995. PMID: 8634716

7

Linkage of posterior polymorphous corneal dystrophy to 20q11.

Héon E, Mathers WD, Alward WL, Weisenthal RW, Sunden SL, Fishbaugh JA, Taylor CM, Krachmer JH, Sheffield VC, Stone EM. Héon E, et al. Hum Mol Genet. 1995 Mar;4(3):485-8. doi: 10.1093/hmg/4.3.485. Hum Mol Genet. 1995. PMID: 7795607

8

Hereditary deep dystrophy of the cornea associated with glaucoma and ruptures in Descemet's membrane.

Rubenstein RA, Silverman JJ. Rubenstein RA, et al. Arch Ophthalmol. 1968 Feb;79(2):123-6. doi: 10.1001/archopht.1968.03850040125002. Arch Ophthalmol. 1968. PMID: 5299826 No abstract available.

9

Congenital endothelial corneal dystrophy. Clinical, pathological, and genetic study.

Pearce WG, Tripathi RC, Morgan G. Pearce WG, et al. Br J Ophthalmol. 1969 Sep;53(9):577-91. doi: 10.1136/bjo.53.9.577. Br J Ophthalmol. 1969. PMID: 4900143 Free PMC article. No abstract available.

10

Hereditary deep dystrophy of the cornea (polymorphous).

Hogan MJ, Bietti G. Hogan MJ, et al. Am J Ophthalmol. 1969 Nov;68(5):777-88. doi: 10.1016/0002-9394(69)94569-3. Am J Ophthalmol. 1969. PMID: 4187513 No abstract available.

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 NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

12 results

Results by year