Salem AK - Search Results

1

Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.

Aldave AJ, Yellore VS, Yu F, Bourla N, Sonmez B, Salem AK, Rayner SA, Sampat KM, Krafchak CM, Richards JE. Aldave AJ, et al. Among authors: salem ak. Am J Med Genet A. 2007 Nov 1;143A(21):2549-56. doi: 10.1002/ajmg.a.31978. Am J Med Genet A. 2007. PMID: 17935237 Free article.

2

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. Among authors: salem ak. Cornea. 2006 May;25(4):413-5. doi: 10.1097/01.ico.0000225260.41594.4a. Cornea. 2006. PMID: 16670477

3

No VSX1 gene mutations associated with keratoconus.

Aldave AJ, Yellore VS, Salem AK, Yoo GL, Rayner SA, Yang H, Tang GY, Piconell Y, Rabinowitz YS. Aldave AJ, et al. Among authors: salem ak. Invest Ophthalmol Vis Sci. 2006 Jul;47(7):2820-2. doi: 10.1167/iovs.05-1530. Invest Ophthalmol Vis Sci. 2006. PMID: 16799019

4

No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy.

Aldave AJ, Rayner SA, Salem AK, Yoo GL, Kim BT, Saeedian M, Sonmez B, Yellore VS. Aldave AJ, et al. Among authors: salem ak. Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3787-90. doi: 10.1167/iovs.05-1635. Invest Ophthalmol Vis Sci. 2006. PMID: 16936088

5

Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.

Aldave AJ, Sonmez B, Bourla N, Schultz G, Papp JC, Salem AK, Rayner SA, Yellore VS. Aldave AJ, et al. Among authors: salem ak. Ophthalmic Genet. 2007 Jun;28(2):57-67. doi: 10.1080/13816810701351321. Ophthalmic Genet. 2007. PMID: 17558846

6

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. Among authors: salem ak. Cornea. 2007 Aug;26(7):896-900. doi: 10.1097/ICO.0b013e318074bb01. Cornea. 2007. PMID: 17667634

7

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. Among authors: salem ak. Cornea. 2007 Sep;26(8):963-5. doi: 10.1097/ICO.0b013e31811dfaf7. Cornea. 2007. PMID: 17721297

8

A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.

Aldave AJ, Yellore VS, Sonmez B, Bourla N, Salem AK, Khan MA, Rayner SA, Glasgow BJ. Aldave AJ, et al. Among authors: salem ak. Arch Ophthalmol. 2008 Mar;126(3):371-7. doi: 10.1001/archopht.126.3.371. Arch Ophthalmol. 2008. PMID: 18332318 Free PMC article.

9

Thyroid-stimulating hormone increases active transport of perchlorate into thyroid cells.

Tran N, Valentín-Blasini L, Blount BC, McCuistion CG, Fenton MS, Gin E, Salem A, Hershman JM. Tran N, et al. Am J Physiol Endocrinol Metab. 2008 Apr;294(4):E802-6. doi: 10.1152/ajpendo.00013.2008. Epub 2008 Feb 26. Am J Physiol Endocrinol Metab. 2008. PMID: 18303123 Free article.

10

Sunitinib inhibits MEK/ERK and SAPK/JNK pathways and increases sodium/iodide symporter expression in papillary thyroid cancer.

Fenton MS, Marion KM, Salem AK, Hogen R, Naeim F, Hershman JM. Fenton MS, et al. Among authors: salem ak. Thyroid. 2010 Sep;20(9):965-74. doi: 10.1089/thy.2010.0008. Thyroid. 2010. PMID: 20629553

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

229 results

Search Page

Filters