EY 08282/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1992	2
1993	2
1996	1
1997	1
1998	1
2000	2
2006	2
2024	0

1

Autosomal dominant cataract: intrafamilial phenotypic variability, interocular asymmetry, and variable progression in four Chilean families.

Shafie SM, Barria von-Bischhoffshausen FR, Bateman JB. Shafie SM, et al. Am J Ophthalmol. 2006 Apr;141(4):750-2. doi: 10.1016/j.ajo.2005.10.050. Am J Ophthalmol. 2006. PMID: 16564818 Free PMC article.

2

A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.

Bateman JB, Geyer DD, Flodman P, Johannes M, Sikela J, Walter N, Moreira AT, Clancy K, Spence MA. Bateman JB, et al. Invest Ophthalmol Vis Sci. 2000 Oct;41(11):3278-85. Invest Ophthalmol Vis Sci. 2000. PMID: 11006214

3

Oculocutaneous albinism: variable expressivity of nystagmus in a sibship.

Cheong PY, King RA, Bateman JB. Cheong PY, et al. J Pediatr Ophthalmol Strabismus. 1992 May-Jun;29(3):185-8. doi: 10.3928/0191-3913-19920501-14. J Pediatr Ophthalmol Strabismus. 1992. PMID: 1432506

4

Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract.

Geyer DD, Spence MA, Johannes M, Flodman P, Clancy KP, Berry R, Sparkes RS, Jonsen MD, Isenberg SJ, Bateman JB. Geyer DD, et al. Am J Ophthalmol. 2006 Apr;141(4):761-3. doi: 10.1016/j.ajo.2005.11.008. Am J Ophthalmol. 2006. PMID: 16564824 Free PMC article.

5

Menkes disease. New ocular and electroretinographic findings.

Ferreira RC, Heckenlively JR, Menkes JH, Bateman JB. Ferreira RC, et al. Ophthalmology. 1998 Jun;105(6):1076-8. doi: 10.1016/S0161-6420(98)96010-9. Ophthalmology. 1998. PMID: 9627659

6

Cataract in early onset and classic Cockayne syndrome.

Ferreira RC, Roeder ER, Bateman JB. Ferreira RC, et al. Ophthalmic Genet. 1997 Dec;18(4):193-7. doi: 10.3109/13816819709041434. Ophthalmic Genet. 1997. PMID: 9457750

7

A new locus for autosomal dominant cataract on chromosome 12q13.

Bateman JB, Johannes M, Flodman P, Geyer DD, Clancy KP, Heinzmann C, Kojis T, Berry R, Sparkes RS, Spence MA. Bateman JB, et al. Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2665-70. Invest Ophthalmol Vis Sci. 2000. PMID: 10937580

8

Assignment of the beta-subunit of rod photoreceptor cGMP phosphodiesterase gene PDEB (homolog of the mouse rd gene) to human chromosome 4p16.

Bateman JB, Klisak I, Kojis T, Mohandas T, Sparkes RS, Li TS, Applebury ML, Bowes C, Farber DB. Bateman JB, et al. Genomics. 1992 Mar;12(3):601-3. doi: 10.1016/0888-7543(92)90454-z. Genomics. 1992. PMID: 1313787

9

Orbital lesions in the blue rubber bleb nevus syndrome.

McCannel CA, Hoenig J, Umlas J, Woog JJ, Newman AN, Bateman JB. McCannel CA, et al. Ophthalmology. 1996 Jun;103(6):933-6. doi: 10.1016/s0161-6420(96)30584-8. Ophthalmology. 1996. PMID: 8643250

10

Assignment of tear lipocalin gene to human chromosome 9q34-9qter.

Glasgow BJ, Heinzmann C, Kojis T, Sparkes RS, Mohandas T, Bateman JB. Glasgow BJ, et al. Curr Eye Res. 1993 Nov;12(11):1019-23. doi: 10.3109/02713689309029229. Curr Eye Res. 1993. PMID: 8306712

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