Dryja TP - Search Results

1

Diagnosis in a patient with fundus albipunctatus and atypical fundus changes.

Hajali M, Fishman GA, Dryja TP, Sweeney MO, Lindeman M. Hajali M, et al. Among authors: dryja tp. Doc Ophthalmol. 2009 Jun;118(3):233-8. doi: 10.1007/s10633-008-9151-8. Epub 2008 Oct 24. Doc Ophthalmol. 2009. PMID: 18949499

2

Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.

Sharon D, Yamamoto H, McGee TL, Rabe V, Szerencsei RT, Winkfein RJ, Prinsen CF, Barnes CS, Andreasson S, Fishman GA, Schnetkamp PP, Berson EL, Dryja TP. Sharon D, et al. Among authors: dryja tp. Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1971-9. Invest Ophthalmol Vis Sci. 2002. PMID: 12037007

3

Novel mutations in the cellular retinaldehyde-binding protein gene (RLBP1) associated with retinitis punctata albescens: evidence of interfamilial genetic heterogeneity and fundus changes in heterozygotes.

Fishman GA, Roberts MF, Derlacki DJ, Grimsby JL, Yamamoto H, Sharon D, Nishiguchi KM, Dryja TP. Fishman GA, et al. Among authors: dryja tp. Arch Ophthalmol. 2004 Jan;122(1):70-5. doi: 10.1001/archopht.122.1.70. Arch Ophthalmol. 2004. PMID: 14718298

4

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.

Dryja TP, McGee TL, Berson EL, Fishman GA, Sandberg MA, Alexander KR, Derlacki DJ, Rajagopalan AS. Dryja TP, et al. Proc Natl Acad Sci U S A. 2005 Mar 29;102(13):4884-9. doi: 10.1073/pnas.0501233102. Epub 2005 Mar 21. Proc Natl Acad Sci U S A. 2005. PMID: 15781871 Free PMC article.

5

Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.

Sweeney MO, McGee TL, Berson EL, Dryja TP. Sweeney MO, et al. Among authors: dryja tp. Mol Vis. 2007 Apr 5;13:588-93. Mol Vis. 2007. PMID: 17438524 Free PMC article.

6

Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene.

Iannaccone A, Tedesco SA, Gallaher KT, Yamamoto H, Charles S, Dryja TP. Iannaccone A, et al. Among authors: dryja tp. Doc Ophthalmol. 2007 Sep;115(2):111-6. doi: 10.1007/s10633-007-9054-0. Epub 2007 May 3. Doc Ophthalmol. 2007. PMID: 17476461

7

Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration.

Deangelis MM, Ji F, Adams S, Morrison MA, Harring AJ, Sweeney MO, Capone A Jr, Miller JW, Dryja TP, Ott J, Kim IK. Deangelis MM, et al. Among authors: dryja tp. Ophthalmology. 2008 Jul;115(7):1209-1215.e7. doi: 10.1016/j.ophtha.2007.10.032. Epub 2007 Dec 27. Ophthalmology. 2008. PMID: 18164066 Free PMC article.

8

Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.

McGee TL, Seyedahmadi BJ, Sweeney MO, Dryja TP, Berson EL. McGee TL, et al. Among authors: dryja tp. J Med Genet. 2010 Jul;47(7):499-506. doi: 10.1136/jmg.2009.075143. Epub 2010 May 27. J Med Genet. 2010. PMID: 20507924 Free PMC article.

9

Intraocular-central nervous system lymphoma: clinical features, diagnosis, and outcomes.

Akpek EK, Ahmed I, Hochberg FH, Soheilian M, Dryja TP, Jakobiec FA, Foster CS. Akpek EK, et al. Among authors: dryja tp. Ophthalmology. 1999 Sep;106(9):1805-10. doi: 10.1016/S0161-6420(99)90341-X. Ophthalmology. 1999. PMID: 10485554

10

Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.

DeAngelis MM, Grimsby JL, Sandberg MA, Berson EL, Dryja TP. DeAngelis MM, et al. Among authors: dryja tp. Arch Ophthalmol. 2002 Mar;120(3):369-75. doi: 10.1001/archopht.120.3.369. Arch Ophthalmol. 2002. PMID: 11879142

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