-
1
-
-
11244318170
-
Congenital stationary night blindness: report of an autosomal recessive family and linkage analysis
-
Abramowicz, M., Ribai, P. Cordonnier, M. 2005 Congenital stationary night blindness: report of an autosomal recessive family and linkage analysis. Am. J. Med. Genet. A 132, 76 79.
-
(2005)
Am. J. Med. Genet. A
, vol.132
, pp. 76-79
-
-
Abramowicz, M.1
Ribai, P.2
Cordonnier, M.3
-
2
-
-
4544288945
-
Autoantibodies against retinal proteins in paraneoplastic and autoimmune retinopathy
-
Adamus, G., Ren, G. Weleber, R. 2004 Autoantibodies against retinal proteins in paraneoplastic and autoimmune retinopathy. BMC Ophthalmol. 4, 5.
-
(2004)
BMC Ophthalmol.
, vol.4
, pp. 5
-
-
Adamus, G.1
Ren, G.2
Weleber, R.3
-
3
-
-
0032944501
-
Vitamin A deficiency in Bangladesh: a review and recommendations for improvement
-
Ahmed, F. 1999 Vitamin A deficiency in Bangladesh: a review and recommendations for improvement. Public Health Nutr. 2, 1 14.
-
(1999)
Public Health Nutr.
, vol.2
, pp. 1-14
-
-
Ahmed, F.1
-
4
-
-
0033662974
-
Vitamin A deficiency in children with acute diarrhoea: a community-based study in Bangladesh
-
Ahmed, F., Rahman, M. Mahmood, C. 2000 Vitamin A deficiency in children with acute diarrhoea: a community-based study in Bangladesh. J. Health Popul. Nutr. 18, 119 122.
-
(2000)
J. Health Popul. Nutr.
, vol.18
, pp. 119-122
-
-
Ahmed, F.1
Rahman, M.2
Mahmood, C.3
-
5
-
-
10644251728
-
Xerophthalmia among hospitalized Iraqi children
-
Al-Kubaisy, W., Al-Rubaiy, M. Nassief, H. 2002 Xerophthalmia among hospitalized Iraqi children. East Mediterr. Health J. 8, 496 502.
-
(2002)
East Mediterr. Health J.
, vol.8
, pp. 496-502
-
-
Al-Kubaisy, W.1
Al-Rubaiy, M.2
Nassief, H.3
-
6
-
-
10744222804
-
Genotype-phenotype correlation in British families with X linked congenital stationary night blindness
-
Allen, L., Zito, I., Bradshaw, K., Patel, R., Bird, A., Fitzke, F., Yates, J., Trump, D., Hardcastle, A. Moore, A. 2003 Genotype-phenotype correlation in British families with X linked congenital stationary night blindness. Br. J. Ophthalmol. 87, 1413 1420.
-
(2003)
Br. J. Ophthalmol.
, vol.87
, pp. 1413-1420
-
-
Allen, L.1
Zito, I.2
Bradshaw, K.3
Patel, R.4
Bird, A.5
Fitzke, F.6
Yates, J.7
Trump, D.8
Hardcastle, A.9
Moore, A.10
-
7
-
-
33750224250
-
Editorial. Reburnishing golden rice
-
Anon 2005 Editorial. Reburnishing golden rice. Nat. Biotechnol. 23, 395.
-
(2005)
Nat. Biotechnol.
, vol.23
, pp. 395
-
-
Anon1
-
8
-
-
23044480031
-
Improvement in visual function and fundus findings for a patient with vitamin A-deficient retinopathy
-
Apushkin, M. Fishman, G. 2005 Improvement in visual function and fundus findings for a patient with vitamin A-deficient retinopathy. Retina 25, 650 652.
-
(2005)
Retina
, vol.25
, pp. 650-652
-
-
Apushkin, M.1
Fishman, G.2
-
9
-
-
0036629927
-
Prevalence of vitamin A deficiency among pre-school and school-aged children in Arssi Zone, Ethiopia
-
Asrat, Y., Omwega, A. Muita, J. 2002 Prevalence of vitamin A deficiency among pre-school and school-aged children in Arssi Zone, Ethiopia. East Afr. Med. J. 79, 355 359.
-
(2002)
East Afr. Med. J.
, vol.79
, pp. 355-359
-
-
Asrat, Y.1
Omwega, A.2
Muita, J.3
-
10
-
-
1542511820
-
Sorsby fundus dystrophy presenting with choroidal neovascularisation showing good response to steroid treatment
-
Atan, D., Evans, C. G., Louis, D. Downes, S. 2004 Sorsby fundus dystrophy presenting with choroidal neovascularisation showing good response to steroid treatment. Br. J. Ophthalmol. 88, 440 441.
-
(2004)
Br. J. Ophthalmol.
, vol.88
, pp. 440-441
-
-
Atan, D.1
Evans, C.G.2
Louis, D.3
Downes, S.4
-
11
-
-
0033986221
-
Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene
-
Ayyagari, R., Griesinger, I., Bingham, E., Lark, K., Moroi, S. Sieving, P. 2000 Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene. Arch. Ophthalmol. 118, 85 92.
-
(2000)
Arch. Ophthalmol.
, vol.118
, pp. 85-92
-
-
Ayyagari, R.1
Griesinger, I.2
Bingham, E.3
Lark, K.4
Moroi, S.5
Sieving, P.6
-
12
-
-
0037261831
-
Glare disability and driving safety
-
Babizhayev, M. 2003 Glare disability and driving safety. Ophthalmic Res. 35, 19 25.
-
(2003)
Ophthalmic Res.
, vol.35
, pp. 19-25
-
-
Babizhayev, M.1
-
13
-
-
84888791395
-
Observations on hemeralopia or nightblindness
-
Baillie, I. 1816 Observations on hemeralopia or nightblindness. Medico-Chirugical J. Rev. 2, 179 182.
-
(1816)
Medico-Chirugical J. Rev.
, vol.2
, pp. 179-182
-
-
Baillie, I.1
-
14
-
-
16844386990
-
A novel TIMP3 mutation associated with Sorsby fundus dystrophy
-
Barbazetto, I., Hayashi, M., Klais, C., Yannuzzi, L. Allikmets, R. 2005 A novel TIMP3 mutation associated with Sorsby fundus dystrophy. Arch. Ophthalmol. 123, 542 543.
-
(2005)
Arch. Ophthalmol.
, vol.123
, pp. 542-543
-
-
Barbazetto, I.1
Hayashi, M.2
Klais, C.3
Yannuzzi, L.4
Allikmets, R.5
-
15
-
-
0036191219
-
A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction
-
Barnes, C., Alexander, K. Fishman, G. 2002 A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction. Ophthalmology 109, 575 583.
-
(2002)
Ophthalmology
, vol.109
, pp. 575-583
-
-
Barnes, C.1
Alexander, K.2
Fishman, G.3
-
16
-
-
3242811338
-
The world through tinted glasses
-
Bennett, D., Webster, G., Molyneux, P., Descamps, M., Plant, G., Pereira, S. Reilly, M. 2004 The world through tinted glasses. Lancet 364, 388
-
(2004)
Lancet
, vol.364
, pp. 388
-
-
Bennett, D.1
Webster, G.2
Molyneux, P.3
Descamps, M.4
Plant, G.5
Pereira, S.6
Reilly, M.7
-
17
-
-
0023697227
-
Vitamin A and vitamin E status of rural preschool children in West Java, Indonesia, and their response to oral doses of vitamin A and of vitamin E
-
Bergen, H. R., Natadisastra, G., Muhilal, H., Dedi, A., Karyadi, D. Olson, J. 1988 Vitamin A and vitamin E status of rural preschool children in West Java, Indonesia, and their response to oral doses of vitamin A and of vitamin E. Am. J. Clin. Nutr. 48, 279 285.
-
(1988)
Am. J. Clin. Nutr.
, vol.48
, pp. 279-285
-
-
Bergen, H.R.1
Natadisastra, G.2
Muhilal, H.3
Dedi, A.4
Karyadi, D.5
Olson, J.6
-
18
-
-
0033994361
-
Extrinsic regulators of epithelial tumor progression: metalloproteinases
-
Bergers, G. Coussens, L. M. 2000 Extrinsic regulators of epithelial tumor progression: metalloproteinases. Curr. Opin. Genet. Dev. 10, 120 127.
-
(2000)
Curr. Opin. Genet. Dev.
, vol.10
, pp. 120-127
-
-
Bergers, G.1
Coussens, L.M.2
-
19
-
-
0029906304
-
Retinitis pigmentosa: unfolding its mystery
-
Berson, E. 1996 Retinitis pigmentosa: unfolding its mystery. Proc. Natl Acad. Sci. U. S. A. 93, 4526 4528.
-
(1996)
Proc. Natl Acad. Sci. U. S. A.
, vol.93
, pp. 4526-4528
-
-
Berson, E.1
-
20
-
-
0033757376
-
Nutrition and retinal degenerations
-
Berson, E. 2000 Nutrition and retinal degenerations. Int. Ophthalmol. Clin. 40, 93 111.
-
(2000)
Int. Ophthalmol. Clin.
, vol.40
, pp. 93-111
-
-
Berson, E.1
-
21
-
-
0027215872
-
A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa
-
Berson, E., Rosner, B., Sandberg, M., Hayes, K. C., Nicholson, B. W., Weigeldifranco, C. Willet, W. 1993 A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa. Arch. Ophthalmol. 111, 1463 1465.
-
(1993)
Arch. Ophthalmol.
, vol.111
, pp. 1463-1465
-
-
Berson, E.1
Rosner, B.2
Sandberg, M.3
Hayes, K.C.4
Nicholson, B.W.5
Weigeldifranco, C.6
Willet, W.7
-
22
-
-
0024339972
-
A prevalence study of vitamin A deficiency and xerophthalmia in northeastern Thailand
-
Bloem, M., Wedel, M., Egger, R., Speek, A., Chusilp, K., Saowakontha, S. Schreurs, W. 1989 A prevalence study of vitamin A deficiency and xerophthalmia in northeastern Thailand. Am. J. Epidemiol. 129, 1095 1103.
-
(1989)
Am. J. Epidemiol.
, vol.129
, pp. 1095-1103
-
-
Bloem, M.1
Wedel, M.2
Egger, R.3
Speek, A.4
Chusilp, K.5
Saowakontha, S.6
Schreurs, W.7
-
23
-
-
4544283939
-
Coping with a nutrient deficiency: cultural models of vitamin A deficiency in northern Niger
-
Blum, L., Pelto, G. Pelto, P. 2004 Coping with a nutrient deficiency: cultural models of vitamin A deficiency in northern Niger. Med. Anthropol. 23, 195 227.
-
(2004)
Med. Anthropol.
, vol.23
, pp. 195-227
-
-
Blum, L.1
Pelto, G.2
Pelto, P.3
-
24
-
-
0030771305
-
Melanoma-associated paraneoplastic retinopathy: case report and review of the literature
-
Boeck, K., Hofmann, S., Klopfer, M., Ian, U., Schmidt, T., Engst, R., Thirkill, C. Ring, J. 1997 Melanoma-associated paraneoplastic retinopathy: case report and review of the literature. Br. J. Dermatol. 137, 457 460.
-
(1997)
Br. J. Dermatol.
, vol.137
, pp. 457-460
-
-
Boeck, K.1
Hofmann, S.2
Klopfer, M.3
Ian, U.4
Schmidt, T.5
Engst, R.6
Thirkill, C.7
Ring, J.8
-
25
-
-
84888785293
-
A family of hemeralopes
-
Bordley, J. 1908 A family of hemeralopes. Bull. Johns Hopkins Hosp. 19, 278 281.
-
(1908)
Bull. Johns Hopkins Hosp.
, vol.19
, pp. 278-281
-
-
Bordley, J.1
-
26
-
-
0026048501
-
Errors in distance appreciation and binocular night vision
-
Bourdy, C., Cottin, F. Monot, A. 1991 Errors in distance appreciation and binocular night vision. Ophthalmic Physiol. Opt. 11, 340 349.
-
(1991)
Ophthalmic Physiol. Opt.
, vol.11
, pp. 340-349
-
-
Bourdy, C.1
Cottin, F.2
Monot, A.3
-
27
-
-
4344602737
-
A comparison of ERG abnormalities in XLRS and XLCSNB
-
Bradshaw, K., Allen, L., Trump, D., Hardcastle, A., George, N. Moore, A. 2004 A comparison of ERG abnormalities in XLRS and XLCSNB. Doc. Ophthalmol. 108, 135 145.
-
(2004)
Doc. Ophthalmol.
, vol.108
, pp. 135-145
-
-
Bradshaw, K.1
Allen, L.2
Trump, D.3
Hardcastle, A.4
George, N.5
Moore, A.6
-
28
-
-
0030321755
-
[Melanoma-associated retinopathy. Apropos of a case and review of the literature]
-
Bret-Dibat, C., Rougier, M., Le Rebeller, M. Delaunay, M. 1996 [Melanoma-associated retinopathy. Apropos of a case and review of the literature]. Bull. Cancer. 83, 1019 1022.
-
(1996)
Bull. Cancer.
, vol.83
, pp. 1019-1022
-
-
Bret-Dibat, C.1
Rougier, M.2
Le Rebeller, M.3
Delaunay, M.4
-
29
-
-
0018373935
-
Vitamin A status of children in Sri Lanka
-
Brink, E., Perera, W., Broske, S., Cash, R., Smith, J., Sauberlich, H. Bashor, M. 1979 Vitamin A status of children in Sri Lanka. Am. J. Clin. Nutr. 32, 84 91.
-
(1979)
Am. J. Clin. Nutr.
, vol.32
, pp. 84-91
-
-
Brink, E.1
Perera, W.2
Broske, S.3
Cash, R.4
Smith, J.5
Sauberlich, H.6
Bashor, M.7
-
30
-
-
0034809225
-
Nyctalopia in antiquity: a review of the ancient Greek, Latin, and Byzantine literature
-
Brouzas, D., Charakidas, A., Vasilakis, M., Nikakis, P. Chatzoulis, D. 2001 Nyctalopia in antiquity: a review of the ancient Greek, Latin, and Byzantine literature. Ophthalmology 108, 1917 1921.
-
(2001)
Ophthalmology
, vol.108
, pp. 1917-1921
-
-
Brouzas, D.1
Charakidas, A.2
Vasilakis, M.3
Nikakis, P.4
Chatzoulis, D.5
-
31
-
-
3242885306
-
Expression of photoreceptor-specific nuclear receptor NR2E3 in rod photoreceptors of fetal human retina
-
Bumsted O'Brien, K., Cheng, H., Jiang, Y., Schulte, D., Swaroop, A. Hendrickson, A. 2004 Expression of photoreceptor-specific nuclear receptor NR2E3 in rod photoreceptors of fetal human retina. Invest. Ophthalmol. Vis. Sci. 45, 2807 2812.
-
(2004)
Invest. Ophthalmol. Vis. Sci.
, vol.45
, pp. 2807-2812
-
-
Bumsted O'Brien, K.1
Cheng, H.2
Jiang, Y.3
Schulte, D.4
Swaroop, A.5
Hendrickson, A.6
-
32
-
-
0033066974
-
Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26
-
Burstedt, M., Sandgren, O., Holmgren, G. Forsman-Semb, K. 1999 Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26. Invest. Ophthalmol. Vis. Sci. 40, 995 1000.
-
(1999)
Invest. Ophthalmol. Vis. Sci.
, vol.40
, pp. 995-1000
-
-
Burstedt, M.1
Sandgren, O.2
Holmgren, G.3
Forsman-Semb, K.4
-
33
-
-
0035125246
-
Ocular phenotype of Bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene
-
Burstedt, M., Forsman-Semb, K., Golovleva, I., Janunger, T., Wachtmeister, L. Sandgren, O. 2001 Ocular phenotype of Bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene. Arch. Ophthalmol. 119, 260 267.
-
(2001)
Arch. Ophthalmol.
, vol.119
, pp. 260-267
-
-
Burstedt, M.1
Forsman-Semb, K.2
Golovleva, I.3
Janunger, T.4
Wachtmeister, L.5
Sandgren, O.6
-
34
-
-
0642311041
-
Retinal function in Bothnia dystrophy. An electrophysiological study
-
Burstedt, M., Sandgren, O., Golovleva, I. Wachtmeister, L. 2003 Retinal function in Bothnia dystrophy. An electrophysiological study. Vision Res. 43, 2559 2571.
-
(2003)
Vision Res.
, vol.43
, pp. 2559-2571
-
-
Burstedt, M.1
Sandgren, O.2
Golovleva, I.3
Wachtmeister, L.4
-
35
-
-
17144396272
-
Associations between specific measures of vision and vision-related quality of life in patients with bothnia dystrophy, a defined type of retinitis pigmentosa
-
Burstedt, M., Monestam, E. Sandgren, O. 2005 Associations between specific measures of vision and vision-related quality of life in patients with bothnia dystrophy, a defined type of retinitis pigmentosa. Retina 25, 317 323.
-
(2005)
Retina
, vol.25
, pp. 317-323
-
-
Burstedt, M.1
Monestam, E.2
Sandgren, O.3
-
36
-
-
0023857467
-
Sorsby's pseudoinflammatory macular dystrophy: Sorsby's fundus dystrophies
-
Capon, M., Polkinghorne, P., Fitzke, F. Bird, A. 1988 Sorsby's pseudoinflammatory macular dystrophy: Sorsby's fundus dystrophies. Eye 2, 114 122.
-
(1988)
Eye
, vol.2
, pp. 114-122
-
-
Capon, M.1
Polkinghorne, P.2
Fitzke, F.3
Bird, A.4
-
37
-
-
0000055594
-
Rhodopsin kinetics and rod adaptation in Oguchi's disease
-
Carr, R. Ripps, H. 1967 Rhodopsin kinetics and rod adaptation in Oguchi's disease. Invest. Ophthalmol. Vis. Sci. 6, 426 436.
-
(1967)
Invest. Ophthalmol. Vis. Sci.
, vol.6
, pp. 426-436
-
-
Carr, R.1
Ripps, H.2
-
38
-
-
0001542078
-
Rhodopsin kinetics and rod adaptation in fundus albipunctatus
-
Carr, R., Ripps, H. Siegel, I. 1974 Rhodopsin kinetics and rod adaptation in fundus albipunctatus. Doc. Ophthalmol. Proc. Ser. 4, 193 204.
-
(1974)
Doc. Ophthalmol. Proc. Ser.
, vol.4
, pp. 193-204
-
-
Carr, R.1
Ripps, H.2
Siegel, I.3
-
39
-
-
0037739966
-
New test to assess pilot's vision following refractive surgery
-
Chisholm, C., Evans, A., Harlow, J. Barbur, J. 2003 New test to assess pilot's vision following refractive surgery. Aviat. Space Environ. Med. 74, 551 559.
-
(2003)
Aviat. Space Environ. Med.
, vol.74
, pp. 551-559
-
-
Chisholm, C.1
Evans, A.2
Harlow, J.3
Barbur, J.4
-
40
-
-
0142257967
-
TIMP-3 mRNA is not overexpressed in Sorsby fundus dystrophy
-
Chong, N., Kvanta, A., Seregard, S., Bird, A., Luthert, P. Steen, B. 2003 TIMP-3 mRNA is not overexpressed in Sorsby fundus dystrophy. Am. J. Ophthalmol. 136, 954 955.
-
(2003)
Am. J. Ophthalmol.
, vol.136
, pp. 954-955
-
-
Chong, N.1
Kvanta, A.2
Seregard, S.3
Bird, A.4
Luthert, P.5
Steen, B.6
-
41
-
-
0036712423
-
Recommendations for indicators: night blindness during pregnancy - a simple tool to assess vitamin A deficiency in a population
-
Christian, P. 2002 Recommendations for indicators: night blindness during pregnancy - a simple tool to assess vitamin A deficiency in a population. J. Nutr. 132, 2884S 2888S.
-
(2002)
J. Nutr.
, vol.132
-
-
Christian, P.1
-
42
-
-
0031892644
-
Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man
-
Cideciyan, A., Zhao, X., Nielsen, L., Khani, S., Jacobson, S. Palczewski, K. 1998 Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man. Proc. Natl Acad. Sci. U. S. A. 95, 328 333.
-
(1998)
Proc. Natl Acad. Sci. U. S. A.
, vol.95
, pp. 328-333
-
-
Cideciyan, A.1
Zhao, X.2
Nielsen, L.3
Khani, S.4
Jacobson, S.5
Palczewski, K.6
-
43
-
-
0034502813
-
Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man
-
Cideciyan, A., Haeseleer, F., Fariss, R., Aleman, T., Jang, G., Verlinde, C., Marmor, M., Jacobson, S. Palczewski, K. 2000 Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man. Vis. Neurosci. 17, 667 678.
-
(2000)
Vis. Neurosci.
, vol.17
, pp. 667-678
-
-
Cideciyan, A.1
Haeseleer, F.2
Fariss, R.3
Aleman, T.4
Jang, G.5
Verlinde, C.6
Marmor, M.7
Jacobson, S.8
Palczewski, K.9
-
44
-
-
0007270540
-
Histoire d'une hemeralopie hereditaire depuis deux siecles dans une famille de la commune de Vendemian pres de Montpelier
-
Cunier, F. 1838 Histoire d'une hemeralopie hereditaire depuis deux siecles dans une famille de la commune de Vendemian pres de Montpelier. Ann. Soc. Med. Gand. 4, 385 395.
-
(1838)
Ann. Soc. Med. Gand.
, vol.4
, pp. 385-395
-
-
Cunier, F.1
-
45
-
-
2442480537
-
Inherited retinal degenerations: therapeutic prospects
-
Delyfer, M., Leveillard, T., Mohand-Said, S., Hicks, D., Picaud, S. Sahel, J. 2004 Inherited retinal degenerations: therapeutic prospects. Biol. Cell. 96, 261 269.
-
(2004)
Biol. Cell.
, vol.96
, pp. 261-269
-
-
Delyfer, M.1
Leveillard, T.2
Mohand-Said, S.3
Hicks, D.4
Picaud, S.5
Sahel, J.6
-
47
-
-
0030035306
-
Vitamin A deficiency and protein-energy malnutrition in a sample of pre-school age children in the Kivu Province in Zaire
-
Donnen, P., Brasseur, D., Dramaix, M., Vertongen, F., Ngoy, B., Zihindula, M. Hennart, P. 1996 Vitamin A deficiency and protein-energy malnutrition in a sample of pre-school age children in the Kivu Province in Zaire. Eur. J. Clin. Nutr. 50, 456 461.
-
(1996)
Eur. J. Clin. Nutr.
, vol.50
, pp. 456-461
-
-
Donnen, P.1
Brasseur, D.2
Dramaix, M.3
Vertongen, F.4
Ngoy, B.5
Zihindula, M.6
Hennart, P.7
-
48
-
-
0033744611
-
Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture
-
Dryja, T. 2000 Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture. Am. J. Ophthalmol. 130, 547 563.
-
(2000)
Am. J. Ophthalmol.
, vol.130
, pp. 547-563
-
-
Dryja, T.1
-
50
-
-
0036206758
-
Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1
-
Eichers, E., Green, J., Stockton, D., Jackman, C., Whelan, J., McNamara, J., Johnson, G., Lupski, J. Katsanis, N. 2002 Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1. Am. J. Hum. Genet. 70, 955 964.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 955-964
-
-
Eichers, E.1
Green, J.2
Stockton, D.3
Jackman, C.4
Whelan, J.5
McNamara, J.6
Johnson, G.7
Lupski, J.8
Katsanis, N.9
-
51
-
-
0034436613
-
Urbanisation and vitamin A deficiency in children: comparison between a traditional district and a new settlement in Mali
-
Farbos, S., Resnikoff, S. Peyramaure, F. 2000 Urbanisation and vitamin A deficiency in children: comparison between a traditional district and a new settlement in Mali. Eur. J. Epidemiol. 16, 1143 1149.
-
(2000)
Eur. J. Epidemiol.
, vol.16
, pp. 1143-1149
-
-
Farbos, S.1
Resnikoff, S.2
Peyramaure, F.3
-
52
-
-
0030046319
-
Acquired unilateral night blindness associated with a negative electroretinogram waveform
-
Fishman, G., Alexander, K., Milam, A. Derlacki, D. 1996 Acquired unilateral night blindness associated with a negative electroretinogram waveform. Ophthalmology 103, 96 104.
-
(1996)
Ophthalmology
, vol.103
, pp. 96-104
-
-
Fishman, G.1
Alexander, K.2
Milam, A.3
Derlacki, D.4
-
53
-
-
0346724556
-
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, G., Roberts, M., Derlacki, D., Grimsby, J., Yamamoto, H., Sharon, D., Nishiguchi, K. Dryja, T. 2004 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. Arch. Ophthalmol. 122, 70 75.
-
(2004)
Arch. Ophthalmol.
, vol.122
, pp. 70-75
-
-
Fishman, G.1
Roberts, M.2
Derlacki, D.3
Grimsby, J.4
Yamamoto, H.5
Sharon, D.6
Nishiguchi, K.7
Dryja, T.8
-
54
-
-
25644436967
-
Biochemical basis for retinol deficiency induced by the I41N and G75D mutations in human plasma retinol-binding protein
-
Folli, C., Viglione, S., Busconi, M. Berni, R. 2005 Biochemical basis for retinol deficiency induced by the I41N and G75D mutations in human plasma retinol-binding protein. Biochem. Biophys. Res. Commun. 336, 1017 1022.
-
(2005)
Biochem. Biophys. Res. Commun.
, vol.336
, pp. 1017-1022
-
-
Folli, C.1
Viglione, S.2
Busconi, M.3
Berni, R.4
-
55
-
-
33544455327
-
Ein Fall von weisspunktiertem Fundus bei Hemeralopie mit Xerose
-
Fuchs, A. 1928 Ein Fall von weisspunktiertem Fundus bei Hemeralopie mit Xerose. Klin. Monatsbl. Augenheilkd. 81, 849 850.
-
(1928)
Klin. Monatsbl. Augenheilkd.
, vol.81
, pp. 849-850
-
-
Fuchs, A.1
-
56
-
-
0000720965
-
White spots of the fundus combined with night blindness and xerosis (Uyemura's syndrome)
-
Fuchs, A. 1959 White spots of the fundus combined with night blindness and xerosis (Uyemura's syndrome). Am. J. Ophthalmol. 48, 101 103.
-
(1959)
Am. J. Ophthalmol.
, vol.48
, pp. 101-103
-
-
Fuchs, A.1
-
57
-
-
0002998903
-
-
Elsevier Science Publishers, Amsterdam, Ch. Acute Vogt-Koyanagi-Harada- like syndrome occurring in a patient with metastatic cutaneous melanoma. pp.
-
Gass, J. 1984 Uveitis Update. Proceedings of the International Symposium on Uveitis-Hanasaari in Espoo, Finland. Elsevier Science Publishers, Amsterdam, Ch. Acute Vogt-Koyanagi-Harada-like syndrome occurring in a patient with metastatic cutaneous melanoma. pp. 407 408.
-
(1984)
Uveitis Update. Proceedings of the International Symposium on Uveitis-Hanasaari in Espoo, Finland
, pp. 407-408
-
-
Gass, J.1
-
58
-
-
0033772292
-
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition
-
Gerber, S., Rozet, J., Takezawa, S., dos Santos, L. C., Lopes, L., Gribouval, O., Penet, C., Perrault, I., Ducroq, D., Souied, E., Jeanpierre, M., Romana, S., Frezal, J., Ferraz, F., Yu-Umesano, R., Munnich, A., Kaplan J. 2000 The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition. Hum. Genet. 107, 276 284.
-
(2000)
Hum. Genet.
, vol.107
, pp. 276-284
-
-
Gerber, S.1
Rozet, J.2
Takezawa, S.3
Dos Santos, L.C.4
Lopes, L.5
Gribouval, O.6
Penet, C.7
Perrault, I.8
Ducroq, D.9
Souied, E.10
Jeanpierre, M.11
Romana, S.12
Frezal, J.13
Ferraz, F.14
Yu-Umesano, R.15
Munnich, A.16
Kaplan, J.17
-
59
-
-
0034831936
-
Electrophysiological findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene
-
Granse, L., Abrahamson, M., Ponjavic, V. Andreasson, S. 2001 Electrophysiological findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene. Ophthalmic Genet. 22, 97 105.
-
(2001)
Ophthalmic Genet.
, vol.22
, pp. 97-105
-
-
Granse, L.1
Abrahamson, M.2
Ponjavic, V.3
Andreasson, S.4
-
60
-
-
0026451346
-
Kearns-Sayre syndrome: a case report and review
-
Gross-Jendroska, M., Schatz, H., McDonald, H. Johnson, R. 1992 Kearns-Sayre syndrome: a case report and review. Eur. J. Ophthalmol. 2, 15 20.
-
(1992)
Eur. J. Ophthalmol.
, vol.2
, pp. 15-20
-
-
Gross-Jendroska, M.1
Schatz, H.2
McDonald, H.3
Johnson, R.4
-
61
-
-
0032953177
-
Treatment of paraneoplastic visual loss with intravenous immunoglobulin: report of 3 cases
-
Guy, J. Aptsiauri, N. 1999 Treatment of paraneoplastic visual loss with intravenous immunoglobulin: report of 3 cases. Arch. Ophthalmol. 117, 471 477.
-
(1999)
Arch. Ophthalmol.
, vol.117
, pp. 471-477
-
-
Guy, J.1
Aptsiauri, N.2
-
62
-
-
0033233359
-
Malnutrition and xerophthalmia in rural communities of Ethiopia
-
Haidar, J. Demissie, T. 1999 Malnutrition and xerophthalmia in rural communities of Ethiopia. East. Afr. Med. J. 76, 590 593.
-
(1999)
East. Afr. Med. J.
, vol.76
, pp. 590-593
-
-
Haida, J.1
Demissie, T.2
-
63
-
-
0033975061
-
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
-
Haider, N., Jacobson, S., Cideciyan, A., Swiderski, R., Streb, L., Searby, C., Beck, G., Hockey, R., Hanna, D., Gorman, S., Duhl, D., Carmi, R., Bennett, J., Weleber, R., Fishman, G., Wright, A., Stone, E. Sheffield, V. 2000 Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate. Nat. Genet. 24, 127 131.
-
(2000)
Nat. Genet.
, vol.24
, pp. 127-131
-
-
Haider, N.1
Jacobson, S.2
Cideciyan, A.3
Swiderski, R.4
Streb, L.5
Searby, C.6
Beck, G.7
Hockey, R.8
Hanna, D.9
Gorman, S.10
Duhl, D.11
Carmi, R.12
Bennett, J.13
Weleber, R.14
Fishman, G.15
Wright, A.16
Stone, E.17
Sheffield, V.18
-
64
-
-
0018826719
-
[Investigation of mesopic vision and sensitivity to glare by means of the new 'nyktometer' (author's transl)]
-
Hartmann, E. Wehmeyer, K. 1980 [Investigation of mesopic vision and sensitivity to glare by means of the new 'nyktometer' (author's transl)]. Klin. Monatsbl. Augenheilkd. 176, 859 863.
-
(1980)
Klin. Monatsbl. Augenheilkd.
, vol.176
, pp. 859-863
-
-
Hartmann, E.1
Wehmeyer, K.2
-
65
-
-
26444609118
-
Optical coherence tomography in enhanced S-cone syndrome: large macular retinoschisis with disorganized retinal lamination
-
Hayashi, T. Kitahara, K. 2005 Optical coherence tomography in enhanced S-cone syndrome: large macular retinoschisis with disorganized retinal lamination. Eur. J. Ophthalmol. 15, 643 646.
-
(2005)
Eur. J. Ophthalmol.
, vol.15
, pp. 643-646
-
-
Hayashi, T.1
Kitahara, K.2
-
66
-
-
28344449263
-
Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity
-
Hayashi, T., Gekka, T., Goto-Omoto, S., Takeuchi, T., Kubo, A. Kitahara, K. 2005 Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity. Ophthalmology 112, 2115 2120.
-
(2005)
Ophthalmology
, vol.112
, pp. 2115-2120
-
-
Hayashi, T.1
Gekka, T.2
Goto-Omoto, S.3
Takeuchi, T.4
Kubo, A.5
Kitahara, K.6
-
68
-
-
0042285484
-
Retinitis pigmentosa: genes, proteins and prospects
-
Hims, M., Diager, S. Inglehearn, C. 2003 Retinitis pigmentosa: genes, proteins and prospects. Dev. Ophthalmol. 37, 109 125.
-
(2003)
Dev. Ophthalmol.
, vol.37
, pp. 109-125
-
-
Hims, M.1
Diager, S.2
Inglehearn, C.3
-
69
-
-
0028927183
-
Enhanced S cone syndrome: evidence for an abnormally large number of S cones
-
Hood, D., Cideciyan, A., Roman, A. Jacobson, S. 1995 Enhanced S cone syndrome: evidence for an abnormally large number of S cones. Vision Res. 35, 1473 1481.
-
(1995)
Vision Res.
, vol.35
, pp. 1473-1481
-
-
Hood, D.1
Cideciyan, A.2
Roman, A.3
Jacobson, S.4
-
70
-
-
33646694881
-
-
Williams & Wilkins, Baltimore, Ch. Paraneoplastic diseases of neuro-ophthalmology interest, pp.
-
Jacobson, D. 1998 Walsh & Hoyt's Clinical Neuro-ophthalmology. Williams & Wilkins, Baltimore, Ch. Paraneoplastic diseases of neuro-ophthalmology interest, pp. 2497 2551.
-
(1998)
Walsh & Hoyt's Clinical Neuro-ophthalmology
, pp. 2497-2551
-
-
Jacobson, D.1
-
71
-
-
4544267698
-
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration
-
Jacobson, S., Aleman, T. S., Cideciyan, A. V., Schwartz, S. B., Roman, A. J., McInnes, R. R., Sheffield, V. C., Stone, E. M., Swaroop, A. Wright, A. F. 2004 Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration. Hum. Mol. Genet. 13, 1893 1902.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1893-1902
-
-
Jacobson, S.1
Aleman, T.S.2
Cideciyan, A.V.3
Schwartz, S.B.4
Roman, A.J.5
McInnes, R.R.6
Sheffield, V.C.7
Stone, E.M.8
Swaroop, A.9
Wright, A.F.10
-
72
-
-
0035077951
-
[Clinical findings in autosomal recessive syndrome of blue cone hypersensitivity]
-
Jurklies, B., Weismann, M., Kellner, U., Zrenner, E. Bornfeld, N. 2001 [Clinical findings in autosomal recessive syndrome of blue cone hypersensitivity]. Ophthalmologe 98, 285 293.
-
(2001)
Ophthalmologe
, vol.98
, pp. 285-293
-
-
Jurklies, B.1
Weismann, M.2
Kellner, U.3
Zrenner, E.4
Bornfeld, N.5
-
73
-
-
3543025207
-
Congenital stationary night blindness and a Schubert-Bornschein type electrophysiology in a family with dominant inheritance
-
Kabanarou, S., Holder, G., Fitzke, F., Bird, A. Webster, A. 2004 Congenital stationary night blindness and a Schubert-Bornschein type electrophysiology in a family with dominant inheritance. Br. J. Ophthalmol. 88, 1018 1022.
-
(2004)
Br. J. Ophthalmol.
, vol.88
, pp. 1018-1022
-
-
Kabanarou, S.1
Holder, G.2
Fitzke, F.3
Bird, A.4
Webster, A.5
-
74
-
-
2942685882
-
Retinitis pigmentosa: understanding the clinical presentation, mechanisms and treatment options
-
Kalloniatis, M. Fletcher, E. 2004 Retinitis pigmentosa: understanding the clinical presentation, mechanisms and treatment options. Clin. Exp. Optom. 87, 65 80.
-
(2004)
Clin. Exp. Optom.
, vol.87
, pp. 65-80
-
-
Kalloniatis, M.1
Fletcher, E.2
-
75
-
-
0032820720
-
TIMP-3 in Bruch's membrane: changes during aging and in age-related macular degeneration
-
Kamei, M. Hollyfield, J. 1999 TIMP-3 in Bruch's membrane: changes during aging and in age-related macular degeneration. Investig. Ophthalmol. Vis. Sci. 40, 2367 2375.
-
(1999)
Investig. Ophthalmol. Vis. Sci.
, vol.40
, pp. 2367-2375
-
-
Kamei, M.1
Hollyfield, J.2
-
76
-
-
0029147010
-
Severe course of cutaneous melanoma associated paraneoplastic retinopathy
-
Kellner, U., Bornfeld, N. Foerster, M. 1995 Severe course of cutaneous melanoma associated paraneoplastic retinopathy. Br. J. Ophthalmol. 79, 746 752.
-
(1995)
Br. J. Ophthalmol.
, vol.79
, pp. 746-752
-
-
Kellner, U.1
Bornfeld, N.2
Foerster, M.3
-
77
-
-
0032133009
-
Cancer-associated retinopathy vs recoverin-associated retinopathy
-
[editorial] [published erratum appears in Am J Ophthalmol 1998;126:866].
-
Keltner, J. Thirkill, C. 1998 Cancer-associated retinopathy vs recoverin-associated retinopathy. Am. J. Ophthalmol. 126, 296 302, [editorial] [published erratum appears in Am J Ophthalmol 1998;126:866].
-
(1998)
Am. J. Ophthalmol.
, vol.126
, pp. 296-302
-
-
Keltner, J.1
Thirkill, C.2
-
78
-
-
0034748752
-
Clinical and immunologic characteristics of melanoma-associated retinopathy syndrome: eleven new cases and a review of 51 previously published cases
-
Keltner, J., Thirkill, C. Yip, P. 2001 Clinical and immunologic characteristics of melanoma-associated retinopathy syndrome: eleven new cases and a review of 51 previously published cases. J. Neuroophthalmol. 21, 173 187.
-
(2001)
J. Neuroophthalmol.
, vol.21
, pp. 173-187
-
-
Keltner, J.1
Thirkill, C.2
Yip, P.3
-
79
-
-
21244441510
-
Vitamin a deficiency in patients with common variable immunodeficiency
-
Kilic, S., Kezer, E., Ilcol, Y., Yakut, T., Aydin, S. Ulus, I. 2005 Vitamin a deficiency in patients with common variable immunodeficiency. J. Clin. Immunol. 25, 275 280.
-
(2005)
J. Clin. Immunol.
, vol.25
, pp. 275-280
-
-
Kilic, S.1
Kezer, E.2
Ilcol, Y.3
Yakut, T.4
Aydin, S.5
Ulus, I.6
-
80
-
-
3142714511
-
Tissue inhibitor of metalloproteinases-3 (TIMP-3) is a binding partner of epithelial growth factor-containing fibulin-like extracellular matrix protein 1 (EFEMP1). Implications for macular degenerations
-
Klenotic, P., Munier, F., Marmorstein, L. Anand-Apte, B. 2004 Tissue inhibitor of metalloproteinases-3 (TIMP-3) is a binding partner of epithelial growth factor-containing fibulin-like extracellular matrix protein 1 (EFEMP1). Implications for macular degenerations. J. Biol. Chem. 279, 30469 30473.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 30469-30473
-
-
Klenotic, P.1
Munier, F.2
Marmorstein, L.3
Anand-Apte, B.4
-
81
-
-
0030776370
-
[Melanoma-associated retinopathy with night blindness. Case report]
-
Klopfer, M., Schmidt, T., Leipert, K., Ugi, I., Boeck, K. Hofmann, S. 1997 [Melanoma-associated retinopathy with night blindness. Case report]. Ophthalmologe 94, 563 567.
-
(1997)
Ophthalmologe
, vol.94
, pp. 563-567
-
-
Klopfer, M.1
Schmidt, T.2
Leipert, K.3
Ugi, I.4
Boeck, K.5
Hofmann, S.6
-
82
-
-
0025805565
-
[Comparative studies of twilight vision with the Mesoptometer I and II and the Nyktometer]
-
Kolling, G. Schratz, B. 1991 [Comparative studies of twilight vision with the Mesoptometer I and II and the Nyktometer]. Fortschr. Ophthalmol. 88, 178 181.
-
(1991)
Fortschr. Ophthalmol.
, vol.88
, pp. 178-181
-
-
Kolling, G.1
Schratz, B.2
-
83
-
-
2942617209
-
Dark adaptation and the retinoid cycle of vision
-
Lamb, T. Pugh, E. N. 2004 Dark adaptation and the retinoid cycle of vision. Prog. Retin. Eye. Res. 23, 307 380.
-
(2004)
Prog. Retin. Eye. Res.
, vol.23
, pp. 307-380
-
-
Lamb, T.1
Pugh, E.N.2
-
84
-
-
0036273213
-
Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type
-
Langrova, H., Gamer, D., Friedburg, C., Besch, D., Zrenner, E. Apfelstedt-Sylla, E. 2002 Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type. Vision Res. 42, 1475 1483.
-
(2002)
Vision Res.
, vol.42
, pp. 1475-1483
-
-
Langrova, H.1
Gamer, D.2
Friedburg, C.3
Besch, D.4
Zrenner, E.5
Apfelstedt-Sylla, E.6
-
85
-
-
0001254382
-
Die sogenannte retinitis punctata albescens
-
Lauber, H. 1910 Die sogenannte retinitis punctata albescens. Klin. Monatsbl. Augenheilkd. 48, 133 148.
-
(1910)
Klin. Monatsbl. Augenheilkd.
, vol.48
, pp. 133-148
-
-
Lauber, H.1
-
86
-
-
20144363752
-
Ocular complications of hypovitaminosis a after bariatric surgery
-
Lee, W., Hamilton, S., Harris, J. Schwab, I. 2005 Ocular complications of hypovitaminosis a after bariatric surgery. Ophthalmology 112, 1031 1034.
-
(2005)
Ophthalmology
, vol.112
, pp. 1031-1034
-
-
Lee, W.1
Hamilton, S.2
Harris, J.3
Schwab, I.4
-
87
-
-
0033988797
-
Human melanoma-associated retinopathy (MAR) antibodies alter the retinal ON-response of the monkey ERG in vivo
-
Lei, B., Bush, R., Milam, A. Sieving, P. 2000 Human melanoma-associated retinopathy (MAR) antibodies alter the retinal ON-response of the monkey ERG in vivo. Invest. Ophthalmol. Vis. Sci. 41, 262 266.
-
(2000)
Invest. Ophthalmol. Vis. Sci.
, vol.41
, pp. 262-266
-
-
Lei, B.1
Bush, R.2
Milam, A.3
Sieving, P.4
-
88
-
-
0029662359
-
[Incomplete congenital stationary night blindness (CSNB). An important differential diagnosis of congenital nystagmus]
-
Lorenz, B., Andrassi, M. Miliczek, K. 1996 [Incomplete congenital stationary night blindness (CSNB). An important differential diagnosis of congenital nystagmus]. Klin. Monatsbl. Augenheilkd. 208, 48 55.
-
(1996)
Klin. Monatsbl. Augenheilkd.
, vol.208
, pp. 48-55
-
-
Lorenz, B.1
Andrassi, M.2
Miliczek, K.3
-
89
-
-
0021021258
-
Vitamin A deficiency in Crohn's disease
-
Main, A., Mills, P., Russell, R., Bronte-Stewart, J., Nelson, L., McLelland, A. Shenkin, A. 1983 Vitamin A deficiency in Crohn's disease. Gut 24, 1169 1175.
-
(1983)
Gut
, vol.24
, pp. 1169-1175
-
-
Main, A.1
Mills, P.2
Russell, R.3
Bronte-Stewart, J.4
Nelson, L.5
McLelland, A.6
Shenkin, A.7
-
90
-
-
0036309004
-
Benign adult familial myoclonic epilepsy (BAFME) with night blindness
-
Manabe, Y., Narai, H., Warita, H., Hayashi, T., Shiro, Y., Sakai, K., Kashihara, K., Shoji, M. Abe, K. 2002 Benign adult familial myoclonic epilepsy (BAFME) with night blindness. Seizure 11, 266 268.
-
(2002)
Seizure
, vol.11
, pp. 266-268
-
-
Manabe, Y.1
Narai, H.2
Warita, H.3
Hayashi, T.4
Shiro, Y.5
Sakai, K.6
Kashihara, K.7
Shoji, M.8
Abe, K.9
-
91
-
-
27544503765
-
Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina
-
Mansergh, F., Orton, N., Vessey, J., Lalonde, M., Stell, W., Tremblay, F., Barnes, S., Rancourt, D. Bech-Hansen, N. 2005 Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina. Hum. Mol. Genet. 14, 3035 3046.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3035-3046
-
-
Mansergh, F.1
Orton, N.2
Vessey, J.3
Lalonde, M.4
Stell, W.5
Tremblay, F.6
Barnes, S.7
Rancourt, D.8
Bech-Hansen, N.9
-
92
-
-
12344275809
-
Vitamin A deficiency and inflammatory markers among preschool children in the Republic of the Marshall Islands
-
Maqsood, M., Dancheck, B., Gamble, M., Palafox, N., Ricks, M., Briand, K. Semba, R. 2004 Vitamin A deficiency and inflammatory markers among preschool children in the Republic of the Marshall Islands. Nutr. J. 3, 21.
-
(2004)
Nutr. J.
, vol.3
, pp. 21
-
-
Maqsood, M.1
Dancheck, B.2
Gamble, M.3
Palafox, N.4
Ricks, M.5
Briand, K.6
Semba, R.7
-
93
-
-
0032243415
-
Standard for clinical electroretinography (1999 update). International Society for Clinical Electrophysiology of Vision
-
Marmor, M. Zrenner, E. 1998 Standard for clinical electroretinography (1999 update). International Society for Clinical Electrophysiology of Vision. Doc. Ophthalmol. 97, 143 156.
-
(1998)
Doc. Ophthalmol.
, vol.97
, pp. 143-156
-
-
Marmor, M.1
Zrenner, E.2
-
94
-
-
0025333641
-
Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivity
-
Marmor, M., Jacobson, S., Foerster, M., Kellner, U. Weleber, R. 1990 Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivity. Am. J. Ophthalmol. 110, 124 134.
-
(1990)
Am. J. Ophthalmol.
, vol.110
, pp. 124-134
-
-
Marmor, M.1
Jacobson, S.2
Foerster, M.3
Kellner, U.4
Weleber, R.5
-
95
-
-
0032990607
-
Topography of cone electrophysiology in the enhanced S cone syndrome
-
Marmor, M., Tan, F., Sutter, E. Bearse, M. A. J. 1999 Topography of cone electrophysiology in the enhanced S cone syndrome. Invest. Ophthalmol. Vis. Sci. 40, 1866 1873.
-
(1999)
Invest. Ophthalmol. Vis. Sci.
, vol.40
, pp. 1866-1873
-
-
Marmor, M.1
Tan, F.2
Sutter, E.3
Bearse, M.A.J.4
-
96
-
-
10944241046
-
Clinical S-cone ERG recording with a commercial hand-held full-field stimulator
-
Marmor, M., Cabael, L., Shukla, S., Hwang, J. Marcus, M. 2004 Clinical S-cone ERG recording with a commercial hand-held full-field stimulator. Doc. Ophthalmol. 109, 101 107.
-
(2004)
Doc. Ophthalmol.
, vol.109
, pp. 101-107
-
-
Marmor, M.1
Cabael, L.2
Shukla, S.3
Hwang, J.4
Marcus, M.5
-
97
-
-
84984763750
-
Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa
-
Maw, M., Kennedy, B., Knight, A., Bridges, R., Roth, K., Mani, E., Mukkadan, J., Nancarrow, D., Crabb, J. Denton, M. 1997 Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa. Nat. Genet. 17, 198 200.
-
(1997)
Nat. Genet.
, vol.17
, pp. 198-200
-
-
Maw, M.1
Kennedy, B.2
Knight, A.3
Bridges, R.4
Roth, K.5
Mani, E.6
Mukkadan, J.7
Nancarrow, D.8
Crabb, J.9
Denton, M.10
-
98
-
-
33646701082
-
Functional observations in vitamin A deficiency: diagnosis and time course of recovery
-
[Epub ahead of print].
-
McBain, V., Egan, C., Pieris, S., Supramaniam, G., Webster, A., Bird, A. Holder, G. 2005 Functional observations in vitamin A deficiency: diagnosis and time course of recovery. Eye. [Epub ahead of print].
-
(2005)
Eye
-
-
McBain, V.1
Egan, C.2
Pieris, S.3
Supramaniam, G.4
Webster, A.5
Bird, A.6
Holder, G.7
-
99
-
-
0025845245
-
Nutritional and household risk factors for xerophthalmia in Aceh, Indonesia: a case-control study. The Aceh Study Group
-
Mele, L., West, K. P. J. K., Pandji, A., Nendrawati, H., Tilden, R. Tarwotjo, I. 1991 Nutritional and household risk factors for xerophthalmia in Aceh, Indonesia: a case-control study. The Aceh Study Group. Am. J. Clin. Nutr. 53, 1460 1465.
-
(1991)
Am. J. Clin. Nutr.
, vol.53
, pp. 1460-1465
-
-
Mele, L.1
West, K.P.J.K.2
Pandji, A.3
Nendrawati, H.4
Tilden, R.5
Tarwotjo, I.6
-
100
-
-
16544364775
-
Vitamin A deficiency in Afghanistan
-
Mihora, L., Jatla, K., Little, T., Campbell, M., Rahim, A. Enzenauer, R. 2004 Vitamin A deficiency in Afghanistan. Eye. Contact. Lens. 30, 159 162.
-
(2004)
Eye. Contact. Lens.
, vol.30
, pp. 159-162
-
-
Mihora, L.1
Jatla, K.2
Little, T.3
Campbell, M.4
Rahim, A.5
Enzenauer, R.6
-
101
-
-
0027400680
-
Autoantibodies against retinal bipolar cells in cutaneous melanoma-associated retinopathy
-
Milam, A., Saari, J., Jacobson, S., Lubinski, W., Feun, L. Alexander, K. 1993 Autoantibodies against retinal bipolar cells in cutaneous melanoma-associated retinopathy. Invest. Ophthalmol. Vis. Sci. 34, 91 100.
-
(1993)
Invest. Ophthalmol. Vis. Sci.
, vol.34
, pp. 91-100
-
-
Milam, A.1
Saari, J.2
Jacobson, S.3
Lubinski, W.4
Feun, L.5
Alexander, K.6
-
102
-
-
18244385003
-
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration
-
Milam, A., Rose, L., Cideciyan, A., Barakat, M., Tang, W., Gupta, N., Aleman, T., Wright, A., Stone, E., Sheffield, V. Jacobson, S. 2002 The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration. Proc. Natl Acad. Sci. U. S. A. 99, 473 478.
-
(2002)
Proc. Natl Acad. Sci. U. S. A.
, vol.99
, pp. 473-478
-
-
Milam, A.1
Rose, L.2
Cideciyan, A.3
Barakat, M.4
Tang, W.5
Gupta, N.6
Aleman, T.7
Wright, A.8
Stone, E.9
Sheffield, V.10
Jacobson, S.11
-
103
-
-
0022528965
-
Congenital stationary night blindness with negative electroretinogram: a new classification
-
Miyake, Y., Yagasaki, K., Horiguchi, M., Kawase, Y. Kanda, T. 1986 Congenital stationary night blindness with negative electroretinogram: a new classification. Arch. Ophthalmol., 1013 1020.
-
(1986)
Arch. Ophthalmol.
, pp. 1013-1020
-
-
Miyake, Y.1
Yagasaki, K.2
Horiguchi, M.3
Kawase, Y.4
Kanda, T.5
-
104
-
-
0028034828
-
Scotopic threshold response in complete and incomplete types of congenital stationary night blindness
-
Miyake, Y., Horiguchi, M., Terasaki, H. Kondo, M. 1994 Scotopic threshold response in complete and incomplete types of congenital stationary night blindness. Invest. Ophthalmol. Vis. Sci. 35, 3770 3775.
-
(1994)
Invest. Ophthalmol. Vis. Sci.
, vol.35
, pp. 3770-3775
-
-
Miyake, Y.1
Horiguchi, M.2
Terasaki, H.3
Kondo, M.4
-
105
-
-
0030431707
-
Electrophysiological findings in patients with Oguchi's disease
-
Miyake, Y., Horiguchi, M., Suzuki, S., Kondo, M. Tanikawa, A. 1996 Electrophysiological findings in patients with Oguchi's disease. Jpn. J. Ophthalmol. 40, 511 519.
-
(1996)
Jpn. J. Ophthalmol.
, vol.40
, pp. 511-519
-
-
Miyake, Y.1
Horiguchi, M.2
Suzuki, S.3
Kondo, M.4
Tanikawa, A.5
-
106
-
-
0342649812
-
A new discovery on dark adaptation in Oguchi's disease. Acta Soc
-
Mizuo, A. 1913 A new discovery on dark adaptation in Oguchi's disease. Acta Soc. Ophthalmol. Jpn. 17, 1148 1150.
-
(1913)
Ophthalmol. Jpn.
, vol.17
, pp. 1148-1150
-
-
Mizuo, A.1
-
107
-
-
0033066801
-
Recessive mutations in the RLBP1 gene encoding cellular retinaldehyde-binding protein in a form of retinitis punctata albescens
-
Morimura, H., Berson, E. Dryja, T. 1999 Recessive mutations in the RLBP1 gene encoding cellular retinaldehyde-binding protein in a form of retinitis punctata albescens. Invest. Ophthalmol. Vis. Sci. 40, 1000 1004.
-
(1999)
Invest. Ophthalmol. Vis. Sci.
, vol.40
, pp. 1000-1004
-
-
Morimura, H.1
Berson, E.2
Dryja, T.3
-
108
-
-
0037465707
-
Mutation in rod PDE6 linked to congenital stationary night blindness impairs the enzyme inhibition by its gamma-subunit
-
Muradov, K., Granovsky, A. Artemyev, N. 2003 Mutation in rod PDE6 linked to congenital stationary night blindness impairs the enzyme inhibition by its gamma-subunit. Biochemistry 42, 3305 3310.
-
(2003)
Biochemistry
, vol.42
, pp. 3305-3310
-
-
Muradov, K.1
Granovsky, A.2
Artemyev, N.3
-
109
-
-
23844446772
-
Vitamin a deficiency and anaemia in young children living in a malaria endemic district of western Kenya
-
Nabakwe, E., Lichtenbelt, W., Ngare, D., Wierik, M., Westerterp, K. Owino, O. 2005 Vitamin a deficiency and anaemia in young children living in a malaria endemic district of western Kenya. East Afr. Med. J. 82, 300 306.
-
(2005)
East Afr. Med. J.
, vol.82
, pp. 300-306
-
-
Nabakwe, E.1
Lichtenbelt, W.2
Ngare, D.3
Wierik, M.4
Westerterp, K.5
Owino, O.6
-
110
-
-
0036143140
-
Macular dystrophy in a 9-year-old boy with fundus albipunctatus
-
Nakamura, M. Miyake, Y. 2002 Macular dystrophy in a 9-year-old boy with fundus albipunctatus. Am. J. Ophthalmol. 133, 278 280.
-
(2002)
Am. J. Ophthalmol.
, vol.133
, pp. 278-280
-
-
Nakamura, M.1
Miyake, Y.2
-
111
-
-
0036202831
-
Enhanced S-cone syndrome with subfoveal neovascularization
-
Nakamura, M., Hotta, Y., Piao, C., Kondo, M., Terasaki, H. Miyake, Y. 2002 Enhanced S-cone syndrome with subfoveal neovascularization. Am. J. Ophthalmol. 133, 575 577.
-
(2002)
Am. J. Ophthalmol.
, vol.133
, pp. 575-577
-
-
Nakamura, M.1
Hotta, Y.2
Piao, C.3
Kondo, M.4
Terasaki, H.5
Miyake, Y.6
-
112
-
-
0042815065
-
RDH5 gene mutations and electroretinogram in fundus albipunctatus with or without macular dystrophy: RDH5 mutations and ERG in fundus albipunctatus
-
Nakamura, M., Skalet, J. Miyake, Y. 2003 RDH5 gene mutations and electroretinogram in fundus albipunctatus with or without macular dystrophy: RDH5 mutations and ERG in fundus albipunctatus. Doc. Ophthalmol. 107, 3 11.
-
(2003)
Doc. Ophthalmol.
, vol.107
, pp. 3-11
-
-
Nakamura, M.1
Skalet, J.2
Miyake, Y.3
-
113
-
-
6344250884
-
Enhanced S-cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X)
-
Nakamura, Y., Hayashi, T., Kozaki, K., Kubo, A., Omoto, S., Watanabe, A., Toda, K., Takeuchi, T., Gekka, T. Kitahara, K. 2004 Enhanced S-cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X). Acta Ophthalmol. Scand. 82, 616 622.
-
(2004)
Acta Ophthalmol. Scand.
, vol.82
, pp. 616-622
-
-
Nakamura, Y.1
Hayashi, T.2
Kozaki, K.3
Kubo, A.4
Omoto, S.5
Watanabe, A.6
Toda, K.7
Takeuchi, T.8
Gekka, T.9
Kitahara, K.10
-
114
-
-
20444475314
-
Novel mutation in RLBP1 gene in a Japanese patient with retinitis punctata albescens
-
Nakamura, M., Lin, J., Ito, Y. Miyake, Y. 2005 Novel mutation in RLBP1 gene in a Japanese patient with retinitis punctata albescens. Am. J. Ophthalmol. 139, 1133 1135.
-
(2005)
Am. J. Ophthalmol.
, vol.139
, pp. 1133-1135
-
-
Nakamura, M.1
Lin, J.2
Ito, Y.3
Miyake, Y.4
-
115
-
-
0001269043
-
A history of congenital stationary night-blindness in nine consecutive generations
-
Nettleship, E. 1907 A history of congenital stationary night-blindness in nine consecutive generations. Trans. Ophthal. Soc. U.K 27, 269 293.
-
(1907)
Trans. Ophthal. Soc. U.K
, vol.27
, pp. 269-293
-
-
Nettleship, E.1
-
116
-
-
0036023650
-
Ocular manifestation of vitamin A deficiency among Orang asli (Aborigine) children in Malaysia
-
Ngah, N., Moktar, N., Isa, N., Selvara, S., Yusof, M., Sani, H., Hasan, Z. Kadir, R. 2002 Ocular manifestation of vitamin A deficiency among Orang asli (Aborigine) children in Malaysia. Asia Pac. J. Clin. Nutr. 11, 88 91.
-
(2002)
Asia Pac. J. Clin. Nutr.
, vol.11
, pp. 88-91
-
-
Ngah, N.1
Moktar, N.2
Isa, N.3
Selvara, S.4
Yusof, M.5
Sani, H.6
Hasan, Z.7
Kadir, R.8
-
117
-
-
18244386256
-
Cone and rod dysfunction in fundus albipunctatus with RDH5 mutation: an electrophysiological study
-
Niwa, Y., Kondo, M., Ueno, S., Nakamura, M., Terasaki, H. Miyake, Y. 2005 Cone and rod dysfunction in fundus albipunctatus with RDH5 mutation: an electrophysiological study. Invest. Ophthalmol. Vis. Sci. 46, 1480 1485.
-
(2005)
Invest. Ophthalmol. Vis. Sci.
, vol.46
, pp. 1480-1485
-
-
Niwa, Y.1
Kondo, M.2
Ueno, S.3
Nakamura, M.4
Terasaki, H.5
Miyake, Y.6
-
118
-
-
0003697825
-
Ueber die eigenartige Hemeralopie mit diffuser weissgraeulicher Verfaerbung des Augenhintergrundes. Graeffe Arch
-
Oguchi, C. 1912 Ueber die eigenartige Hemeralopie mit diffuser weissgraeulicher Verfaerbung des Augenhintergrundes. Graeffe Arch. Ophthalmology 81, 109 117.
-
(1912)
Ophthalmology
, vol.81
, pp. 109-117
-
-
Oguchi, C.1
-
119
-
-
17444382738
-
Relationship between retinopathy and cirrhosis
-
Onder, C., Bengur, T., Selcuk, D., Bulent, S., Belkis, U., Ahmet, M., Eser, P. Leyla, A. 2005 Relationship between retinopathy and cirrhosis. World J. Gastroenterol. 11, 2193 2196.
-
(2005)
World J. Gastroenterol.
, vol.11
, pp. 2193-2196
-
-
Onder, C.1
Bengur, T.2
Selcuk, D.3
Bulent, S.4
Belkis, U.5
Ahmet, M.6
Eser, P.7
Leyla, A.8
-
120
-
-
0037328379
-
Vitamin A status and nutritional intake of carotenoids of preschool children in Ijaye Orile community in Nigeria
-
Oso, O., Abiodun, P., Omotade, O. Oyewole, D. 2003 Vitamin A status and nutritional intake of carotenoids of preschool children in Ijaye Orile community in Nigeria. J. Trop. Pediatr. 49, 42 47.
-
(2003)
J. Trop. Pediatr.
, vol.49
, pp. 42-47
-
-
Oso, O.1
Abiodun, P.2
Omotade, O.3
Oyewole, D.4
-
121
-
-
0024269064
-
Retinitis pigmentosa
-
Pagon, R. 1988 Retinitis pigmentosa. Surv. Ophthalmol. 33, 137 177.
-
(1988)
Surv. Ophthalmol.
, vol.33
, pp. 137-177
-
-
Pagon, R.1
-
122
-
-
0021813206
-
Night blindness after jejunoileal bypass surgery
-
Parker, W., Clorfeine, G. Longstreth, G. 1985 Night blindness after jejunoileal bypass surgery. Am. J. Gastroenterol. 80, 535 537.
-
(1985)
Am. J. Gastroenterol.
, vol.80
, pp. 535-537
-
-
Parker, W.1
Clorfeine, G.2
Longstreth, G.3
-
123
-
-
21444449325
-
Integrating strategies for combating vitamin A deficiency: successes in Asia
-
de Pee, S., Bloem, M., Kiess, L., Panagides, D. Talukder, A. 2003 Integrating strategies for combating vitamin A deficiency: successes in Asia. Forum Nutr. 56, 210 212.
-
(2003)
Forum Nutr.
, vol.56
, pp. 210-212
-
-
De Pee, S.1
Bloem, M.2
Kiess, L.3
Panagides, D.4
Talukder, A.5
-
124
-
-
17144382013
-
Choroidal neovascularization in Sorsby fundus dystrophy treated with photodynamic therapy and intravitreal triamcinolone acetonide
-
Peiretti, E., Klancnik, J. M. J., Spaide, R. Yannuzzi, L. 2005 Choroidal neovascularization in Sorsby fundus dystrophy treated with photodynamic therapy and intravitreal triamcinolone acetonide. Retina 25, 377 379.
-
(2005)
Retina
, vol.25
, pp. 377-379
-
-
Peiretti, E.1
Klancnik, J.M.J.2
Spaide, R.3
Yannuzzi, L.4
-
125
-
-
15544371180
-
The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes
-
Peng, G., Ahmad, O., Ahmad, F., Liu, J. Chen, S. 2005 The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes. Hum. Mol. Genet. 14, 747 764.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 747-764
-
-
Peng, G.1
Ahmad, O.2
Ahmad, F.3
Liu, J.4
Chen, S.5
-
126
-
-
0020687174
-
Night vision in a case of vitamin A deficiency due to malabsorption
-
Perlman, I., Barzilai, D., Haim, T. Schramek, A. 1983 Night vision in a case of vitamin A deficiency due to malabsorption. Br. J. Ophthalmol. 67, 37 42.
-
(1983)
Br. J. Ophthalmol.
, vol.67
, pp. 37-42
-
-
Perlman, I.1
Barzilai, D.2
Haim, T.3
Schramek, A.4
-
127
-
-
4644359289
-
Measuring visual acuity-mesopic or photopic conditions, and high or low contrast letters
-
Pesudovs, K., Marsack, J., Donnelly, W., Thibos, L. Applegate, R. 2004 Measuring visual acuity-mesopic or photopic conditions, and high or low contrast letters J. Refract. Surg. 20, 0S508 OS514.
-
(2004)
J. Refract. Surg.
, vol.20
-
-
Pesudovs, K.1
Marsack, J.2
Donnelly, W.3
Thibos, L.4
Applegate, R.5
-
128
-
-
23844530361
-
Central and paracentral visual field defects and driving abilities
-
Petzold, A. Plant, G. 2005 Central and paracentral visual field defects and driving abilities. Ophthalmologica 219, 191 201.
-
(2005)
Ophthalmologica
, vol.219
, pp. 191-201
-
-
Petzold, A.1
Plant, G.2
-
129
-
-
0041633694
-
Melanoma-associated retinopathy: high frequency of subclinical findings in patients with melanoma
-
Pfohler, C., Haus, A., Palmowski, A., Ugurel, S., Ruprecht, K., Thirkill, C., Tilgen, W. Reinhold, U. 2003 Melanoma-associated retinopathy: high frequency of subclinical findings in patients with melanoma. Br. J. Dermatol. 149, 74 78.
-
(2003)
Br. J. Dermatol.
, vol.149
, pp. 74-78
-
-
Pfohler, C.1
Haus, A.2
Palmowski, A.3
Ugurel, S.4
Ruprecht, K.5
Thirkill, C.6
Tilgen, W.7
Reinhold, U.8
-
130
-
-
0034622122
-
A brief review of retinitis pigmentosa and the identified retinitis pigmentosa genes
-
Phelan, J. Bok, D. 2000 A brief review of retinitis pigmentosa and the identified retinitis pigmentosa genes. Mol. Vis. 6, 116 124.
-
(2000)
Mol. Vis.
, vol.6
, pp. 116-124
-
-
Phelan, J.1
Bok, D.2
-
131
-
-
24144490359
-
The role of retinal adaptation in night driving
-
Plainis, S., Murray, I. Charman, W. 2005 The role of retinal adaptation in night driving. Optom. Vis. Sci. 82, 682 688.
-
(2005)
Optom. Vis. Sci.
, vol.82
, pp. 682-688
-
-
Plainis, S.1
Murray, I.2
Charman, W.3
-
132
-
-
0029068542
-
Recoverin, a photoreceptor-specific calcium-binding protein, is expressed by the tumor of a patient with cancer-associated retinopathy
-
Polans, A., Witkowska, D., Haley, T., Amundson, D., Baizer, L. Adamus, G. 1995 Recoverin, a photoreceptor-specific calcium-binding protein, is expressed by the tumor of a patient with cancer-associated retinopathy. Proc. Natl Acad. Sci. U. S. A. 92, 9176 9180.
-
(1995)
Proc. Natl Acad. Sci. U. S. A.
, vol.92
, pp. 9176-9180
-
-
Polans, A.1
Witkowska, D.2
Haley, T.3
Amundson, D.4
Baizer, L.5
Adamus, G.6
-
133
-
-
0024830978
-
Sorsby's fundus dystrophy: a clinical study
-
Polkinghorne, P., Capon, M., Berninger, T., Lyness, A., Sehmi, K. Bird, A. 1989 Sorsby's fundus dystrophy: a clinical study. Ophthalmology 96, 1763 1768.
-
(1989)
Ophthalmology
, vol.96
, pp. 1763-1768
-
-
Polkinghorne, P.1
Capon, M.2
Berninger, T.3
Lyness, A.4
Sehmi, K.5
Bird, A.6
-
134
-
-
6344244475
-
Mesopic contrast sensitivity in the presence or absence of glare in a large driver population
-
Puell, M., Palomo, C., Sanchez-Ramos, C. Villena, C. 2004 Mesopic contrast sensitivity in the presence or absence of glare in a large driver population. Graefes Arch. Clin. Exp. Ophthalmol. 242, 755 761.
-
(2004)
Graefes Arch. Clin. Exp. Ophthalmol.
, vol.242
, pp. 755-761
-
-
Puell, M.1
Palomo, C.2
Sanchez-Ramos, C.3
Villena, C.4
-
135
-
-
0032909366
-
Through a shade darkly
-
Purvin, V. 1999 Through a shade darkly. Surv. Ophthalmol. 43, 335 340.
-
(1999)
Surv. Ophthalmol.
, vol.43
, pp. 335-340
-
-
Purvin, V.1
-
136
-
-
0036689164
-
[Hypovitaminosis A in Brazil: a public health problem]
-
Ramalho, R., Flores, H. Saunders, C. 2002 [Hypovitaminosis A in Brazil: a public health problem]. Rev. Panam. Salud. Publica. 12, 117 122.
-
(2002)
Rev. Panam. Salud. Publica.
, vol.12
, pp. 117-122
-
-
Ramalho, R.1
Flores, H.2
Saunders, C.3
-
137
-
-
0031062879
-
[Dark adaptation for evaluating visual performance at twilight using the Trendelenburg eyeglasses]
-
Reiner, J. 1997 [Dark adaptation for evaluating visual performance at twilight using the Trendelenburg eyeglasses]. Klin. Monatsbl. Augenheilkd. 210, 111 112.
-
(1997)
Klin. Monatsbl. Augenheilkd.
, vol.210
, pp. 111-112
-
-
Reiner, J.1
-
138
-
-
0026547608
-
Assessment of vitamin A deficiency in the Republic of Djibouti
-
Resnikoff, S., Filliard, G., Carlier, C., Luzeau, R. Amedee-Manesme, O. 1992 Assessment of vitamin A deficiency in the Republic of Djibouti. Eur. J. Clin. Nutr. 46, 25 30.
-
(1992)
Eur. J. Clin. Nutr.
, vol.46
, pp. 25-30
-
-
Resnikoff, S.1
Filliard, G.2
Carlier, C.3
Luzeau, R.4
Amedee-Manesme, O.5
-
139
-
-
0021273908
-
Functional abnormalities in vincristine-induced night blindness
-
Ripps, H., Carr, R., Siegel, I. Greenstein, V. 1984 Functional abnormalities in vincristine-induced night blindness. Invest. Ophthalmol. 25, 787 794.
-
(1984)
Invest. Ophthalmol.
, vol.25
, pp. 787-794
-
-
Ripps, H.1
Carr, R.2
Siegel, I.3
Greenstein, V.4
-
140
-
-
5444266028
-
Recombinant AAV-mediated gene transfer to the retina: gene therapy perspectives
-
Rolling, F. 2004 Recombinant AAV-mediated gene transfer to the retina: gene therapy perspectives. Gene. Ther. 11 Suppl. 1 0S26 OS32.
-
(2004)
Gene. Ther.
, vol.11
, Issue.1
-
-
Rolling, F.1
-
141
-
-
0028298989
-
Risk factors for vitamin A deficiency in rural areas of the Philippines
-
Rosen, D., Sloan, N., del Rosario, A. de la Paz, T. 1994 Risk factors for vitamin A deficiency in rural areas of the Philippines. J. Trop. Pediatr. 40, 82 87.
-
(1994)
J. Trop. Pediatr.
, vol.40
, pp. 82-87
-
-
Rosen, D.1
Sloan, N.2
Del Rosario, A.3
De La Paz, T.4
-
142
-
-
0030060021
-
Vitamin A deficiency and xerophthalmia in western Yemen
-
Rosen, D., al Sharif, Z., Bashir, M., al Shabooti, A. Pizzarello, L. 1996 Vitamin A deficiency and xerophthalmia in western Yemen. Eur. J. Clin. Nutr. 50, 54 57.
-
(1996)
Eur. J. Clin. Nutr.
, vol.50
, pp. 54-57
-
-
Rosen, D.1
Al Sharif, Z.2
Bashir, M.3
Al Shabooti, A.4
Pizzarello, L.5
-
143
-
-
0029016649
-
[Paraneoplastic retinopathy associated with cutaneous melanoma. An update apropos of a case]
-
Rougier, M., Hostyn, P., Bret-Dibat, C., Delaunay, M., Riss, I. Le Rebeller, M. 1995 [Paraneoplastic retinopathy associated with cutaneous melanoma. An update apropos of a case]. J. Fr. Ophtalmol. 18, 396 403.
-
(1995)
J. Fr. Ophtalmol.
, vol.18
, pp. 396-403
-
-
Rougier, M.1
Hostyn, P.2
Bret-Dibat, C.3
Delaunay, M.4
Riss, I.5
Le Rebeller, M.6
-
144
-
-
33646686453
-
[Severe bilateral ocular affection caused by vitamin A deficiency.]
-
Ruiz-Martin, M., Boto-de Los-Bueis, A. Romero-Martin, R. 2005 [Severe bilateral ocular affection caused by vitamin A deficiency.]. Arch. Soc. Esp. Oftalmol. 80, 663 666.
-
(2005)
Arch. Soc. Esp. Oftalmol.
, vol.80
, pp. 663-666
-
-
Ruiz-Martin, M.1
Boto-de Los-Bueis, A.2
Romero-Martin, R.3
-
145
-
-
12144279532
-
Gestational nightblindness among women attending a public maternity hospital in Rio de Janeiro, Brazil
-
Saunders, C., do Carmo Leal, M., Gomes, M., Campos, L., de Santos Silva, B., Thiapo dos Lima, A. Ramalho, R. 2004 Gestational nightblindness among women attending a public maternity hospital in Rio de Janeiro, Brazil. J. Health Popul. Nutr. 22, 348 356.
-
(2004)
J. Health Popul. Nutr.
, vol.22
, pp. 348-356
-
-
Saunders, C.1
Do Carmo Leal, M.2
Gomes, M.3
Campos, L.4
De Santos Silva, B.5
Thiapo Dos Lima, A.6
Ramalho, R.7
-
146
-
-
0017065470
-
Blindness caused by photoreceptor degeneration as a remote effect of cancer
-
Sawyer, R., Selhorst, J. B., Zimmerman, L. E., Hoyt, W. F. 1976 Blindness caused by photoreceptor degeneration as a remote effect of cancer. Am. J. Ophthalmol. 81, 606 613.
-
(1976)
Am. J. Ophthalmol.
, vol.81
, pp. 606-613
-
-
Sawyer, R.1
Selhorst, J.B.2
Zimmerman, L.E.3
Hoyt, W.F.4
-
147
-
-
0029828841
-
Risk factors for xerophthalmia in the Republic of Kiribati
-
Schaumberg, D., O'Connor, J. Semba, R. 1996 Risk factors for xerophthalmia in the Republic of Kiribati. Eur. J. Clin. Nutr. 50, 761 764.
-
(1996)
Eur. J. Clin. Nutr.
, vol.50
, pp. 761-764
-
-
Schaumberg, D.1
O'Connor, J.2
Semba, R.3
-
148
-
-
0036789046
-
Prevalence of undernutrition and vitamin A deficiency in the Dogon Region, Mali
-
Schemann, J., Banou, A., Guindo, A., Joret, V., Traore, L. Malvy, D. 2002 Prevalence of undernutrition and vitamin A deficiency in the Dogon Region, Mali. J. Am. Coll. Nutr. 21, 381 387.
-
(2002)
J. Am. Coll. Nutr.
, vol.21
, pp. 381-387
-
-
Schemann, J.1
Banou, A.2
Guindo, A.3
Joret, V.4
Traore, L.5
Malvy, D.6
-
149
-
-
0027549912
-
Elderly drivers in Germany-fitness and driving behavior
-
Schlag, B. 1993 Elderly drivers in Germany-fitness and driving behavior. Accid. Anal. Prev. 25, 47 55.
-
(1993)
Accid. Anal. Prev.
, vol.25
, pp. 47-55
-
-
Schlag, B.1
-
150
-
-
0030738749
-
Mesopic vision in myopia corrected by photorefractive keratectomy, soft contact lenses, and spectacles
-
Schlote, T., Kriegerowski, M., Bende, T., Derse, M., Thiel, H. Jean, B. 1997 Mesopic vision in myopia corrected by photorefractive keratectomy, soft contact lenses, and spectacles. J. Cataract Refract. Surg. 23, 718 725.
-
(1997)
J. Cataract Refract. Surg.
, vol.23
, pp. 718-725
-
-
Schlote, T.1
Kriegerowski, M.2
Bende, T.3
Derse, M.4
Thiel, H.5
Jean, B.6
-
151
-
-
77951374758
-
Beitrag zur Analyse des menschlichen Electroretinogram
-
Schubert, G. Bornschein, H. 1952 Beitrag zur Analyse des menschlichen Electroretinogram. Ophthalmologica 123, 396 413.
-
(1952)
Ophthalmologica
, vol.123
, pp. 396-413
-
-
Schubert, G.1
Bornschein, H.2
-
152
-
-
0347513286
-
Risk factors for nightblindness among women of childbearing age in Cambodia
-
Semba, R., de Pee, S., Panagides, D., Poly, O. Bloem, M. 2003 Risk factors for nightblindness among women of childbearing age in Cambodia. Eur. J. Clin. Nutr. 57, 1627 1632.
-
(2003)
Eur. J. Clin. Nutr.
, vol.57
, pp. 1627-1632
-
-
Semba, R.1
De Pee, S.2
Panagides, D.3
Poly, O.4
Bloem, M.5
-
153
-
-
0141722455
-
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration
-
Sharon, D., Sandberg, M., Caruso, R., Berson, E. Dryja, T. 2003 Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration. Arch. Ophthalmol. 121, 1316 1323.
-
(2003)
Arch. Ophthalmol.
, vol.121
, pp. 1316-1323
-
-
Sharon, D.1
Sandberg, M.2
Caruso, R.3
Berson, E.4
Dryja, T.5
-
154
-
-
0025357734
-
Mechanisms and sites of loss of scotopic sensitivity: a clinical analysis of congenital stationary night blindness
-
Sharp, D., Arden, G., Kemp, C., Hogg, C. Bird, A. 1990 Mechanisms and sites of loss of scotopic sensitivity: a clinical analysis of congenital stationary night blindness. Clin. Vision Sci. 5, 217 230.
-
(1990)
Clin. Vision Sci.
, vol.5
, pp. 217-230
-
-
Sharp, D.1
Arden, G.2
Kemp, C.3
Hogg, C.4
Bird, A.5
-
155
-
-
26944468018
-
Xerophthalmia: a study among malnourished children of West Mednipur District
-
Shaw, C., Islam, M., Chakroborty, M., Biswas, M., Ghosh, T. Biswas, G. 2005 Xerophthalmia: a study among malnourished children of West Mednipur District. J. Indian Med. Assoc. 103, 182 183.
-
(2005)
J. Indian Med. Assoc.
, vol.103
, pp. 182-183
-
-
Shaw, C.1
Islam, M.2
Chakroborty, M.3
Biswas, M.4
Ghosh, T.5
Biswas, G.6
-
156
-
-
5744234955
-
Vitamin A deficiency and xerophthalmia among school-aged children in Southeastern Asia
-
Singh, V. West, K. P. 2004 Vitamin A deficiency and xerophthalmia among school-aged children in Southeastern Asia. Eur. J. Clin. Nutr. 58, 1342 1349.
-
(2004)
Eur. J. Clin. Nutr.
, vol.58
, pp. 1342-1349
-
-
Singh, V.1
West, K.P.2
-
158
-
-
0015612015
-
Luminance-dependent changes in mesopic visual contrast sensitivity
-
Smith, R. A. J. 1973 Luminance-dependent changes in mesopic visual contrast sensitivity. J. Physiol. 230, 115 135.
-
(1973)
J. Physiol.
, vol.230
, pp. 115-135
-
-
Smith, R.A.J.1
-
160
-
-
0003900413
-
Vitamin A Deficiency and Its Consequences
-
3rd edition. WHO, Geneva.
-
Somner, A. 1995 Vitamin A Deficiency and Its Consequences. A Field Guide to Detection and Control. 3rd edition. WHO, Geneva.
-
(1995)
A Field Guide to Detection and Control
-
-
Somner, A.1
-
161
-
-
0001790180
-
A fundus dystrophy with unusual features
-
Sorsby, A. Mason, M. 1949 A fundus dystrophy with unusual features. Br. J. Ophthalmol. 33, 67 97.
-
(1949)
Br. J. Ophthalmol.
, vol.33
, pp. 67-97
-
-
Sorsby, A.1
Mason, M.2
-
162
-
-
0030042489
-
Retinitis punctata albescens associated with the Arg135Trp mutation in the rhodopsin gene
-
Souied, E., Soubrane, G., Benlian, P., Coscas, G., Gerber, S., Munnich, A. Kaplan, J. 1996 Retinitis punctata albescens associated with the Arg135Trp mutation in the rhodopsin gene. Am. J. Ophthalmol. 121, 19 25.
-
(1996)
Am. J. Ophthalmol.
, vol.121
, pp. 19-25
-
-
Souied, E.1
Soubrane, G.2
Benlian, P.3
Coscas, G.4
Gerber, S.5
Munnich, A.6
Kaplan, J.7
-
163
-
-
0003701494
-
-
3rd edn. Elsevier, Mosby.
-
Spalton, D., Hitchings, R. Hunter, P. 2005 Atlas of Clinical Ophthalmology, 3rd edn. Elsevier, Mosby.
-
(2005)
Atlas of Clinical Ophthalmology
-
-
Spalton, D.1
Hitchings, R.2
Hunter, P.3
-
164
-
-
1842452669
-
Rapid recovery of night blindness due to obesity surgery after vitamin A repletion therapy
-
Spits, Y., De Laey, J. Leroy, B. 2004 Rapid recovery of night blindness due to obesity surgery after vitamin A repletion therapy. Br. J. Ophthalmol. 88, 583 585.
-
(2004)
Br. J. Ophthalmol.
, vol.88
, pp. 583-585
-
-
Spits, Y.1
De Laey, J.2
Leroy, B.3
-
165
-
-
84888782490
-
On epithehal xerosis of the conjunctiva
-
Stephenson, S. 1896 On epithehal xerosis of the conjunctiva. Trans Ophthalmol. Soc. UK 18, 55 102.
-
(1896)
Trans Ophthalmol. Soc. UK
, vol.18
, pp. 55-102
-
-
Stephenson, S.1
-
166
-
-
33646705622
-
Into the twilight zone: the complexities of mesopic vision and luminous efficiency
-
Stockman, A. Sharpe, L. T. 2006 Into the twilight zone: the complexities of mesopic vision and luminous efficiency. Ophthal. Physiol. Opt. 26, 225 239.
-
(2006)
Ophthal. Physiol. Opt.
, vol.26
, pp. 225-239
-
-
Stockman, A.1
Sharpe, L.T.2
-
167
-
-
0031668129
-
A novel splice site mutation in the tissue inhibitor of the metalloproteinases-3 gene in Sorsby's fundus dystrophy with unusual clinical features
-
Tabata, Y., Isashiki, Y., Kamimura, K., Nakao, K. Ohba, N. 1998 A novel splice site mutation in the tissue inhibitor of the metalloproteinases-3 gene in Sorsby's fundus dystrophy with unusual clinical features. Hum. Genet. 103, 179 182.
-
(1998)
Hum. Genet.
, vol.103
, pp. 179-182
-
-
Tabata, Y.1
Isashiki, Y.2
Kamimura, K.3
Nakao, K.4
Ohba, N.5
-
168
-
-
0035318618
-
Light adaptation in motion direction judgments
-
Takeuchi, T., De Valois, K. Motoyoshi, I. 2001 Light adaptation in motion direction judgments. J. Opt. Soc. Am. A Opt. Image. Sci. Vis. 18, 755 764.
-
(2001)
J. Opt. Soc. Am. A Opt. Image. Sci. Vis.
, vol.18
, pp. 755-764
-
-
Takeuchi, T.1
De Valois, K.2
Motoyoshi, I.3
-
169
-
-
4744345997
-
The night vision threshold test is a better predictor of low serum vitamin A concentration than self-reported night blindness in pregnant urban Nepalese women
-
Taren, D., Duncan, B., Shrestha, K., Shrestha, N., Genaro-Wolf, D., Schleicher, R., Pfeiffer, C., Sowell, A., Greivenkamp, J. Canfield, L. 2004 The night vision threshold test is a better predictor of low serum vitamin A concentration than self-reported night blindness in pregnant urban Nepalese women. J. Nutr. 134, 2573 2578.
-
(2004)
J. Nutr.
, vol.134
, pp. 2573-2578
-
-
Taren, D.1
Duncan, B.2
Shrestha, K.3
Shrestha, N.4
Genaro-Wolf, D.5
Schleicher, R.6
Pfeiffer, C.7
Sowell, A.8
Greivenkamp, J.9
Canfield, L.10
-
170
-
-
0026712288
-
The cancer-associated retinopathy antigen is a recoverin-like protein
-
Thirkill, C., Tait, R., Tyler, N., Roth, A. Keltner, J. 1992 The cancer-associated retinopathy antigen is a recoverin-like protein. Invest. Ophthalmol. Vis. Sci. 33, 2768 2772.
-
(1992)
Invest. Ophthalmol. Vis. Sci.
, vol.33
, pp. 2768-2772
-
-
Thirkill, C.1
Tait, R.2
Tyler, N.3
Roth, A.4
Keltner, J.5
-
171
-
-
0021195426
-
The epidemiology of vitamin A deficiency and xerophthalmia
-
Tielsch, J. Sommer, a 1984 The epidemiology of vitamin A deficiency and xerophthalmia. Ann. Rev. Nutr. 4, 183 205.
-
(1984)
Ann. Rev. Nutr.
, vol.4
, pp. 183-205
-
-
Tielsch, J.1
Sommer, A.2
-
172
-
-
0022976023
-
Prevalence and severity of xerophthalmia in southern Malawi
-
Tielsch, J., West, K. P. J., Katz, J., Chirambo, M., Schwab, L., Johnson, G., Tizazu, T., Swartwood, J. Sommer, A. 1986 Prevalence and severity of xerophthalmia in southern Malawi. Am. J. Epidemiol. 124, 561 568.
-
(1986)
Am. J. Epidemiol.
, vol.124
, pp. 561-568
-
-
Tielsch, J.1
West, K.P.J.2
Katz, J.3
Chirambo, M.4
Schwab, L.5
Johnson, G.6
Tizazu, T.7
Swartwood, J.8
Sommer, A.9
-
173
-
-
0347985508
-
Vitamin A deficiency disorders: international efforts to control a preventable pox
-
Underwood, B. 2004 Vitamin A deficiency disorders: international efforts to control a preventable pox. J. Nutr. 134, 231S 236S.
-
(2004)
J. Nutr.
, vol.134
-
-
Underwood, B.1
-
174
-
-
10644291682
-
Ocular fundus images by scanning laser ophthalmoscopy in a patient with enhanced S-cone syndrome
-
Usui, T., Ichibe, M., Tanimoto, N., Ueki, S., Takagi, M., Hasegawa, S., Abe, H., Miyagawa, Y. Nakazawa, M. 2004 Ocular fundus images by scanning laser ophthalmoscopy in a patient with enhanced S-cone syndrome. Retina 24, 946 952.
-
(2004)
Retina
, vol.24
, pp. 946-952
-
-
Usui, T.1
Ichibe, M.2
Tanimoto, N.3
Ueki, S.4
Takagi, M.5
Hasegawa, S.6
Abe, H.7
Miyagawa, Y.8
Nakazawa, M.9
-
175
-
-
0000328618
-
Ueber eine merkwurdige Augenhintergrundveraenerung bei zwei Faellen von idiopathischer Hemerlopie
-
Uyemura, M. 1928 Ueber eine merkwurdige Augenhintergrundveraenerung bei zwei Faellen von idiopathischer Hemerlopie. Klin. Monatsbl. Augenheilkd. 81, 471 473.
-
(1928)
Klin. Monatsbl. Augenheilkd.
, vol.81
, pp. 471-473
-
-
Uyemura, M.1
-
176
-
-
17844366281
-
Adult blindness secondary to vitamin A deficiency associated with an eating disorder
-
Velasco Cruz, A., Attie-Castro, F., Fernandes, S., Cortes, J., de Tarso P Pierre-Filho, P., Rocha, E. Marchini, J. 2005 Adult blindness secondary to vitamin A deficiency associated with an eating disorder. Nutrition 21, 630 633.
-
(2005)
Nutrition
, vol.21
, pp. 630-633
-
-
Velasco Cruz, A.1
Attie-Castro, F.2
Fernandes, S.3
Cortes, J.4
De Tarso P Pierre-Filho, P.5
Rocha, E.6
Marchini, J.7
-
177
-
-
0035714394
-
Florent Cunier [1812-1852]. A tragic figure in ophthalmic history
-
Wayenborgh, J. P. 2001 Florent Cunier [1812-1852]. A tragic figure in ophthalmic history. Strabismus 9, 177 178.
-
(2001)
Strabismus
, vol.9
, pp. 177-178
-
-
Wayenborgh, J.P.1
-
178
-
-
0028097367
-
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy
-
Weber, B., Vogt, G., Pruett, R., Stohr, H. Felbor, U. 1994 Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy. Nat. Genet. 8, 352 356.
-
(1994)
Nat. Genet.
, vol.8
, pp. 352-356
-
-
Weber, B.1
Vogt, G.2
Pruett, R.3
Stohr, H.4
Felbor, U.5
-
179
-
-
0033759537
-
Prevalence of eye diseases in primary school children in a rural area of Tanzania
-
Wedner, S., Ross, D., Balira, R., Kaji, L. Foster, A. 2000 Prevalence of eye diseases in primary school children in a rural area of Tanzania. Br. J. Ophthalmol. 84, 1291 1297.
-
(2000)
Br. J. Ophthalmol.
, vol.84
, pp. 1291-1297
-
-
Wedner, S.1
Ross, D.2
Balira, R.3
Kaji, L.4
Foster, A.5
-
180
-
-
0027965653
-
Paraneoplastic retinopathy associated with antiretinal bipolar cell antibodies in cutaneous malignant melanoma
-
Weinstein, J., Kelman, S., Bresnick, G. Kornguth, S. 1994 Paraneoplastic retinopathy associated with antiretinal bipolar cell antibodies in cutaneous malignant melanoma. Ophthalmology 101, 1236 1243.
-
(1994)
Ophthalmology
, vol.101
, pp. 1236-1243
-
-
Weinstein, J.1
Kelman, S.2
Bresnick, G.3
Kornguth, S.4
-
181
-
-
0025717905
-
Low vision management of retinitis pigmentosa
-
Weiss, N. 1991 Low vision management of retinitis pigmentosa. J. Am. Optom. Assoc. 62, 42 52.
-
(1991)
J. Am. Optom. Assoc.
, vol.62
, pp. 42-52
-
-
Weiss, N.1
-
182
-
-
0026689964
-
Panstromal Schnyder's corneal dystrophy. Ultrastructural and histochemical studies
-
Weiss, J., Rodrigues, M., Kruth, H., Rajagopalan, S., Rader, D. Kachadoorian, H. 1992 Panstromal Schnyder's corneal dystrophy. Ultrastructural and histochemical studies. Ophthalmology 99, 1072 1081.
-
(1992)
Ophthalmology
, vol.99
, pp. 1072-1081
-
-
Weiss, J.1
Rodrigues, M.2
Kruth, H.3
Rajagopalan, S.4
Rader, D.5
Kachadoorian, H.6
-
183
-
-
0000336286
-
-
Mosby-Year Book (eds S. J. Ryan, T. E. Ogden, A. P. Schachat, R. P. Murphy, B. M. Glaser, A. Patz, S. J. M. D. Ryan Mosby
-
Weleber, R. 1994 Retinitis pigmentosa and allied disorders. In: Mosby-Year Book (eds S. J. Ryan, T. E. Ogden, A. P. Schachat, R. P. Murphy, B. M. Glaser, A. Patz, S. J. M. D. Ryan Mosby, pp. 335 466.
-
(1994)
Retinitis pigmentosa and allied disorders
, pp. 335-466
-
-
Weleber, R.1
-
184
-
-
0036068117
-
Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture)
-
Weleber, R. 2002 Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture). Ophthalmic Genet. 23, 71 97.
-
(2002)
Ophthalmic Genet.
, vol.23
, pp. 71-97
-
-
Weleber, R.1
-
185
-
-
0017874747
-
A historical note on the mode of administration of vitamin A for the cure of night blindness
-
Wolf, G. 1978 A historical note on the mode of administration of vitamin A for the cure of night blindness. Am. J. Clin. Nutr. 31, 290 292.
-
(1978)
Am. J. Clin. Nutr.
, vol.31
, pp. 290-292
-
-
Wolf, G.1
-
186
-
-
0030187692
-
A history of vitamin A and retinoids
-
Wolf, G. 1996 A history of vitamin A and retinoids. FASEB 10, 1102 1107.
-
(1996)
FASEB
, vol.10
, pp. 1102-1107
-
-
Wolf, G.1
-
187
-
-
0030036138
-
Selective damage to either the 'M' or 'P' pathway in human retinal disease: implications for visual processing
-
Wolfe, J. E., Arden, G. B. Plant, G. T. 1996 Selective damage to either the 'M' or 'P' pathway in human retinal disease: implications for visual processing. Eur J Ophthalmol 6, 208 214.
-
(1996)
Eur J Ophthalmol
, vol.6
, pp. 208-214
-
-
Wolfe, J.E.1
Arden, G.B.2
Plant, G.T.3
-
188
-
-
24144483416
-
Standard measures of visual acuity do not predict drivers' recognition performance under day or night conditions
-
Wood, J. Owens, D. 2005 Standard measures of visual acuity do not predict drivers' recognition performance under day or night conditions. Optom. Vis. Sci. 82, 698 705.
-
(2005)
Optom. Vis. Sci.
, vol.82
, pp. 698-705
-
-
Wood, J.1
Owens, D.2
-
189
-
-
4544264183
-
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome
-
Wright, A., Reddick, A., Schwartz, S., Ferguson, J., Aleman, T., Kellner, U., Jurklies, B., Schuster, A., Zrenner, E., Wissinger, B., Lennon, A., Shu, X., Cideciyan, A., Stone, E., Jacobson, S. Swaroop, A. 2004 Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome. Hum. Mutat. 24, 439 450.
-
(2004)
Hum. Mutat.
, vol.24
, pp. 439-450
-
-
Wright, A.1
Reddick, A.2
Schwartz, S.3
Ferguson, J.4
Aleman, T.5
Kellner, U.6
Jurklies, B.7
Schuster, A.8
Zrenner, E.9
Wissinger, B.10
Lennon, A.11
Shu, X.12
Cideciyan, A.13
Stone, E.14
Jacobson, S.15
Swaroop, A.16
-
190
-
-
0035991631
-
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina
-
Wutz, K., Sauer, C., Zrenner, E., Lorenz, B., Alitalo, T., Broghammer, M., Hergersberg, M., de la Chapelle, A., Weber, B., Wissinger, B., Meindl, A. Pusch, C. 2002 Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina. Eur. J. Hum. Genet. 10, 449 456.
-
(2002)
Eur. J. Hum. Genet.
, vol.10
, pp. 449-456
-
-
Wutz, K.1
Sauer, C.2
Zrenner, E.3
Lorenz, B.4
Alitalo, T.5
Broghammer, M.6
Hergersberg, M.7
De La Chapelle, A.8
Weber, B.9
Wissinger, B.10
Meindl, A.11
Pusch, C.12
-
191
-
-
0033199547
-
Electroretinograms and visual evoked potentials elicited by spectral stimuli in a patient with enhanced S-cone syndrome
-
Yamamoto, S., Hayashi, M. Takeuchi, S. 1999 Electroretinograms and visual evoked potentials elicited by spectral stimuli in a patient with enhanced S-cone syndrome. Jpn. J. Ophthalmol. 43, 433 437.
-
(1999)
Jpn. J. Ophthalmol.
, vol.43
, pp. 433-437
-
-
Yamamoto, S.1
Hayashi, M.2
Takeuchi, S.3
-
192
-
-
33644701685
-
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram
-
Zeitz, C., van Genderen, M., Neidhardt, J., Luhmann, U., Hoeben, F., Forster, U., Wycisk, K., Matyas, G., Hoyng, C., Riemslag, F., Meire, F., Cremers, F. Berger, W. 2005 Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. Invest. Ophthalmol. Vis. Sci. 46, 4328 4335.
-
(2005)
Invest. Ophthalmol. Vis. Sci.
, vol.46
, pp. 4328-4335
-
-
Zeitz, C.1
Van Genderen, M.2
Neidhardt, J.3
Luhmann, U.4
Hoeben, F.5
Forster, U.6
Wycisk, K.7
Matyas, G.8
Hoyng, C.9
Riemslag, F.10
Meire, F.11
Cremers, F.12
Berger, W.13
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