Thompson D - Search Results

1

Severe microcornea with anterior segment malformation in a mother and her son.

Russell-Eggitt I, Kriss A, Restori M, Speedwell L, Thompson D, Timms C, Yu C. Russell-Eggitt I, et al. Among authors: thompson d. Acta Ophthalmol Scand Suppl. 1996;(219):27-9. doi: 10.1111/j.1600-0420.1996.tb00379.x. Acta Ophthalmol Scand Suppl. 1996. PMID: 8741112

2

Modulation of amblyopia therapy following early surgery for unilateral congenital cataracts.

Lloyd IC, Dowler JG, Kriss A, Speedwell L, Thompson DA, Russell-Eggitt I, Taylor D. Lloyd IC, et al. Among authors: thompson da. Br J Ophthalmol. 1995 Sep;79(9):802-6. doi: 10.1136/bjo.79.9.802. Br J Ophthalmol. 1995. PMID: 7488596 Free PMC article.

3

Electrophysiological and eye-movement abnormalities in children with the Bardet-Biedl syndrome.

Lavy T, Harris CM, Shawkat F, Thompson D, Taylor D, Kriss A. Lavy T, et al. Among authors: thompson d. J Pediatr Ophthalmol Strabismus. 1995 Nov-Dec;32(6):364-7. doi: 10.3928/0191-3913-19951101-08. J Pediatr Ophthalmol Strabismus. 1995. PMID: 8587019

4

Visual acuity in unilateral cataract.

Thompson DA, Møller H, Russell-Eggitt I, Kriss A. Thompson DA, et al. Br J Ophthalmol. 1996 Sep;80(9):794-8. doi: 10.1136/bjo.80.9.794. Br J Ophthalmol. 1996. PMID: 8942375 Free PMC article. Clinical Trial.

5

Achiasmia in a case of midline craniofacial cleft with seesaw nystagmus.

Leitch RJ, Thompson D, Harris CM, Chong K, Russell-Eggitt I, Kriss A. Leitch RJ, et al. Among authors: thompson d. Br J Ophthalmol. 1996 Nov;80(11):1023-4. doi: 10.1136/bjo.80.11.1023-a. Br J Ophthalmol. 1996. PMID: 8976735 Free PMC article. No abstract available.

6

The optokinetic response differences between congenital profound and nonprofound unilateral visual deprivation.

Shawkat FS, Harris CM, Taylor DS, Thompson DA, Russell-Eggitt I, Kriss A. Shawkat FS, et al. Among authors: thompson da. Ophthalmology. 1995 Nov;102(11):1615-22. doi: 10.1016/s0161-6420(95)30819-6. Ophthalmology. 1995. PMID: 9098252

7

Early VEP and ERG evidence of visual dysfunction in autosomal recessive osteopetrosis.

Thompson DA, Kriss A, Taylor D, Russell-Eggitt I, Hodgkins P, Morgan G, Vellodi A, Gerritsen EJ. Thompson DA, et al. Neuropediatrics. 1998 Jun;29(3):137-44. doi: 10.1055/s-2007-973550. Neuropediatrics. 1998. PMID: 9706624

8

Gaze evoked amaurosis in neurofibromatosis type II.

Smith L, Kriss A, Gregson R, Thompson D, Taylor D. Smith L, et al. Among authors: thompson d. Br J Ophthalmol. 1998 May;82(5):584-5. doi: 10.1136/bjo.82.5.584. Br J Ophthalmol. 1998. PMID: 9713069 Free PMC article. No abstract available.

9

Familial congenital saccade initiation failure and isolated cerebellar vermis hypoplasia.

Harris CM, Hodgkins PR, Kriss A, Chong WK, Thompson DA, Mezey LE, Shawkat FS, Taylor DS, Wilson J. Harris CM, et al. Among authors: thompson da. Dev Med Child Neurol. 1998 Nov;40(11):775-9. doi: 10.1111/j.1469-8749.1998.tb12347.x. Dev Med Child Neurol. 1998. PMID: 9881808 Free article.

10

A case of reversible blindness in maple syrup urine disease.

Backhouse O, Leitch RJ, Thompson D, Kriss A, Charris D, Clayton P, Russell-Eggitt I. Backhouse O, et al. Among authors: thompson d. Br J Ophthalmol. 1999 Feb;83(2):250-1. doi: 10.1136/bjo.83.2.250. Br J Ophthalmol. 1999. PMID: 10396207 Free PMC article. No abstract available.

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