Stone E - Search Results

1

Familial non-arteritic anterior ischemic optic neuropathy.

Hayreh SS, Fingert JH, Stone E, Jacobson DM. Hayreh SS, et al. Among authors: stone e. Graefes Arch Clin Exp Ophthalmol. 2008 Sep;246(9):1295-305. doi: 10.1007/s00417-008-0853-0. Epub 2008 Jun 28. Graefes Arch Clin Exp Ophthalmol. 2008. PMID: 18587597

2

Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation.

Stone EM, Newman NJ, Miller NR, Johns DR, Lott MT, Wallace DC. Stone EM, et al. J Clin Neuroophthalmol. 1992 Mar;12(1):10-4. J Clin Neuroophthalmol. 1992. PMID: 1532593

3

Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene.

Stone EM, Kimura AE, Nichols BE, Khadivi P, Fishman GA, Sheffield VC. Stone EM, et al. Ophthalmology. 1991 Dec;98(12):1806-13. doi: 10.1016/s0161-6420(91)32046-3. Ophthalmology. 1991. PMID: 1775314

4

Difficulty differentiating Leber's from dominant optic neuropathy in a patient with remote visual loss.

Jacobson DM, Stone EM. Jacobson DM, et al. Among authors: stone em. J Clin Neuroophthalmol. 1991 Sep;11(3):152-7. J Clin Neuroophthalmol. 1991. PMID: 1836796

5

Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy.

Stone EM, Coppinger JM, Kardon RH, Donelson J. Stone EM, et al. Arch Ophthalmol. 1990 Oct;108(10):1417-20. doi: 10.1001/archopht.1990.01070120065030. Arch Ophthalmol. 1990. PMID: 1977373

6

Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.

Fishman GA, Stone E, Gilbert LD, Vandenburgh K, Sheffield VC, Heckenlively JR. Fishman GA, et al. Among authors: stone e. Ophthalmology. 1994 Aug;101(8):1409-21. doi: 10.1016/s0161-6420(94)31156-0. Ophthalmology. 1994. PMID: 8058286

7

Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma.

Johnson AT, Drack AV, Kwitek AE, Cannon RL, Stone EM, Alward WL. Johnson AT, et al. Among authors: stone em. Ophthalmology. 1993 Apr;100(4):524-9. doi: 10.1016/s0161-6420(13)31615-7. Ophthalmology. 1993. PMID: 8479711

8

Identification of a gene that causes primary open angle glaucoma.

Stone EM, Fingert JH, Alward WL, Nguyen TD, Polansky JR, Sunden SL, Nishimura D, Clark AF, Nystuen A, Nichols BE, Mackey DA, Ritch R, Kalenak JW, Craven ER, Sheffield VC. Stone EM, et al. Science. 1997 Jan 31;275(5300):668-70. doi: 10.1126/science.275.5300.668. Science. 1997. PMID: 9005853

9

Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1).

Brown J Jr, Fingert JH, Taylor CM, Lake M, Sheffield VC, Stone EM. Brown J Jr, et al. Among authors: stone em. Arch Ophthalmol. 1997 Jan;115(1):95-9. doi: 10.1001/archopht.1997.01100150097016. Arch Ophthalmol. 1997. PMID: 9006432

10

Serine-27-phenylalanine mutation within the peripherin/RDS gene in a family with cone dystrophy.

Fishman GA, Stone EM, Alexander KR, Gilbert LD, Derlacki DJ, Butler NS. Fishman GA, et al. Among authors: stone em. Ophthalmology. 1997 Feb;104(2):299-306. doi: 10.1016/s0161-6420(97)30320-0. Ophthalmology. 1997. PMID: 9052636

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