Snead MP - Search Results

1

Cyclocryotherapy for chronic glaucoma after vitreoretinal surgery.

Chee CK, Snead MP, Scott JD. Chee CK, et al. Among authors: snead mp. Eye (Lond). 1994;8 ( Pt 4):414-8. doi: 10.1038/eye.1994.98. Eye (Lond). 1994. PMID: 7821463

2

White light interferometry in amblyopic children--a pilot study.

Vernon SA, Hardman-Lea S, Rubinstein MP, Snead MP. Vernon SA, et al. Among authors: snead mp. Eye (Lond). 1990;4 ( Pt 6):802-5. doi: 10.1038/eye.1990.126. Eye (Lond). 1990. PMID: 2101110

3

Calculated versus A-scan result for axial length using different types of ultrasound probe tip.

Snead MP, Rubinstein MP, Lea SH, Haworth SM. Snead MP, et al. Eye (Lond). 1990;4 ( Pt 5):718-22. doi: 10.1038/eye.1990.101. Eye (Lond). 1990. PMID: 2282947

4

Thrombolysis in patients with diabetes. More evidence that the treatment should not necessarily be withheld.

Newman DK, Snead MP, Flanagan DW, Scott JD. Newman DK, et al. Among authors: snead mp. BMJ. 1995 Apr 15;310(6985):1008. doi: 10.1136/bmj.310.6985.1008a. BMJ. 1995. PMID: 7728007 Free PMC article. No abstract available.

5

Stickler syndrome: correlation between vitreoretinal phenotypes and linkage to COL 2A1.

Snead MP, Payne SJ, Barton DE, Yates JR, al-Imara L, Pope FM, Scott JD. Snead MP, et al. Eye (Lond). 1994;8 ( Pt 6):609-14. doi: 10.1038/eye.1994.153. Eye (Lond). 1994. PMID: 7867814

6

Vitreous detachment and the posterior hyaloid membrane: a clinicopathological study.

Snead MP, Snead DR, Mahmood AS, Scott JD. Snead MP, et al. Among authors: snead dr. Eye (Lond). 1994;8 ( Pt 2):204-9. doi: 10.1038/eye.1994.47. Eye (Lond). 1994. PMID: 7958023

7

The pseudo-posterior limiting layer syndrome: a vitreoretinal heredodegeneration with autosomal dominant transmission. Graefe's Arch Clin Exp Ophthalmol (1994) 232:16-24.

Snead MP, Newmann DK, Poulson A, Scott JD. Snead MP, et al. Graefes Arch Clin Exp Ophthalmol. 1995 Dec;233(12):805-6. doi: 10.1007/BF00184095. Graefes Arch Clin Exp Ophthalmol. 1995. PMID: 8626092 No abstract available.

8

Stickler syndrome type 2 and linkage to the COL11A1 gene.

Snead MP, Yates JR, Williams R, Payne SJ, Pope FM, Scott JD. Snead MP, et al. Ann N Y Acad Sci. 1996 Jun 8;785:331-2. doi: 10.1111/j.1749-6632.1996.tb56300.x. Ann N Y Acad Sci. 1996. PMID: 8702171 No abstract available.

9

A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagen.

Richards AJ, Yates JR, Williams R, Payne SJ, Pope FM, Scott JD, Snead MP. Richards AJ, et al. Among authors: snead mp. Hum Mol Genet. 1996 Sep;5(9):1339-43. doi: 10.1093/hmg/5.9.1339. Hum Mol Genet. 1996. PMID: 8872475

10

Masked confirmation of linkage between type 1 congenital vitreous anomaly and COL 2A1 in Stickler syndrome.

Snead MP, Yates JR, Pope FM, Temple IK, Scott JD. Snead MP, et al. Graefes Arch Clin Exp Ophthalmol. 1996 Nov;234(11):720-1. doi: 10.1007/BF00292360. Graefes Arch Clin Exp Ophthalmol. 1996. PMID: 8950594 No abstract available.

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