-
1
-
-
0016134917
-
Congenital stationary night blindness
-
R.E. Carr Congenital stationary night blindness Trans Am Ophthalmol Soc 72 1974 448 487
-
(1974)
Trans Am Ophthalmol Soc
, vol.72
, pp. 448-487
-
-
Carr, R.E.1
-
2
-
-
0022528965
-
Congenital stationary night blindness with negative electroretinogram: A new classification
-
Y. Miyake, K. Yagasaki, M. Horiguchi, Y. Kawase, T. Kanda Congenital stationary night blindness with negative electroretinogram A new classification Arch Ophthalmol 104 7 1986 1013 1020 (Pubitemid 16062068)
-
(1986)
Archives of Ophthalmology
, vol.104
, Issue.7
, pp. 1013-1020
-
-
Miyake, Y.1
Yagasaki, K.2
Horiguchi, M.3
-
3
-
-
0001883810
-
The basis of clinical electroretinography
-
G. Karpe The basis of clinical electroretinography Acta Ophthalmol 24 suppl 1945 1 118
-
(1945)
Acta Ophthalmol
, vol.24
, Issue.SUPPL.
, pp. 1-118
-
-
Karpe, G.1
-
4
-
-
77951374758
-
Analysis of the human electroretinogram
-
G. Schubert, H. Bornschein Analysis of the human electroretinogram Ophthalmologica 123 6 1952 396 413
-
(1952)
Ophthalmologica
, vol.123
, Issue.6
, pp. 396-413
-
-
Schubert, G.1
Bornschein, H.2
-
5
-
-
38049001481
-
The negative ERG: Clinical phenotypes and disease mechanisms of inner retinal dysfunction
-
I. Audo, A.G. Robson, G.E. Holder, A.T. Moore The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction Surv Ophthalmol 53 1 2008 16 40
-
(2008)
Surv Ophthalmol
, vol.53
, Issue.1
, pp. 16-40
-
-
Audo, I.1
Robson, A.G.2
Holder, G.E.3
Moore, A.T.4
-
6
-
-
0023146464
-
On- and off-responses in photopic electroretinogram in complete and incomplete types of congenital stationary night blindness
-
Y. Miyake, K. Yagasaki, M. Horiguchi, Y. Kawase On- and off-responses in photopic electroretinogram in complete and incomplete types of congenital stationary night blindness Jpn J Ophthalmol 31 1 1987 81 87 (Pubitemid 17036452)
-
(1987)
Japanese Journal of Ophthalmology
, vol.31
, Issue.1
, pp. 81-87
-
-
Miyake, Y.1
Yagasaki, K.2
Horiguchi, M.3
Kawase, Y.4
-
7
-
-
0036273213
-
Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type
-
DOI 10.1016/S0042-6989(02)00068-8, PII S0042698902000688
-
H. Langrová, D. Gamer, C. Friedburg, D. Besch, E. Zrenner, E. Apfelstedt-Sylla Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type Vision Res 42 11 2002 1475 1483 (Pubitemid 34603546)
-
(2002)
Vision Research
, vol.42
, Issue.11
, pp. 1475-1483
-
-
Langrova, H.1
Gamer, D.2
Friedburg, C.3
Besch, D.4
Zrenner, E.5
Apfelstedt-Sylla, E.6
-
8
-
-
0033757466
-
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
-
N.T. Bech-Hansen, M.J. Naylor, T.A. Maybaum Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness Nat Genet 26 3 2000 319 323
-
(2000)
Nat Genet
, vol.26
, Issue.3
, pp. 319-323
-
-
Bech-Hansen, N.T.1
Naylor, M.J.2
Maybaum, T.A.3
-
9
-
-
33644701685
-
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram
-
DOI 10.1167/iovs.05-0526
-
C. Zeitz, M. van Genderen, J. Neidhardt Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram Invest Ophthalmol Vis Sci 46 11 2005 4328 4335 (Pubitemid 44264639)
-
(2005)
Investigative Ophthalmology and Visual Science
, vol.46
, Issue.11
, pp. 4328-4335
-
-
Zeitz, C.1
Van Genderen, M.2
Neidhardt, J.3
Luhmann, U.F.O.4
Hoeben, F.5
Forster, U.6
Wycisk, K.7
Matyas, G.8
Hoyng, C.B.9
Riemslag, F.10
Meire, F.11
Cremers, F.P.M.12
Berger, W.13
-
10
-
-
16344363011
-
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6
-
DOI 10.1073/pnas.0501233102
-
T.P. Dryja, T.L. McGee, E.L. Berson Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6 Proc Natl Acad Sci U S A 102 13 2005 4884 4889 (Pubitemid 40471548)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.13
, pp. 4884-4889
-
-
Dryja, T.P.1
McGee, T.L.2
Berson, E.L.3
Fishman, G.A.4
Sandberg, M.A.5
Alexander, K.R.6
Derlacki, D.J.7
Rajagopalan, A.S.8
-
11
-
-
72149101903
-
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness
-
I. Audo, S. Kohl, B.P. Leroy TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness Am J Hum Genet 85 5 2009 720 729
-
(2009)
Am J Hum Genet
, vol.85
, Issue.5
, pp. 720-729
-
-
Audo, I.1
Kohl, S.2
Leroy, B.P.3
-
12
-
-
71849089234
-
Recessive mutations of the gene TRPM1 abrogate on bipolar cell function and cause complete congenital stationary night blindness in humans
-
Z. Li, P.I. Sergouniotis, M. Michaelides Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans Am J Hum Genet 85 5 2009 711 719
-
(2009)
Am J Hum Genet
, vol.85
, Issue.5
, pp. 711-719
-
-
Li, Z.1
Sergouniotis, P.I.2
Michaelides, M.3
-
13
-
-
71849117485
-
Mutations in TRPM1 are a common cause of complete congenital stationary night blindness
-
M.M. van Genderen, M.M. Bijveld, Y.B. Claassen Mutations in TRPM1 are a common cause of complete congenital stationary night blindness Am J Hum Genet 85 5 2009 730 736
-
(2009)
Am J Hum Genet
, vol.85
, Issue.5
, pp. 730-736
-
-
Van Genderen, M.M.1
Bijveld, M.M.2
Claassen, Y.B.3
-
14
-
-
77952315144
-
TRPM1 mutations are associated with the complete form of congenital stationary night blindness
-
M. Nakamura, R. Sanuki, T.R. Yasuma TRPM1 mutations are associated with the complete form of congenital stationary night blindness Mol Vis 16 2010 425 437
-
(2010)
Mol Vis
, vol.16
, pp. 425-437
-
-
Nakamura, M.1
Sanuki, R.2
Yasuma, T.R.3
-
15
-
-
84856843254
-
GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness
-
N.S. Peachey, T.A. Ray, R. Florijn GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness Am J Hum Genet 90 2 2012 331 339
-
(2012)
Am J Hum Genet
, vol.90
, Issue.2
, pp. 331-339
-
-
Peachey, N.S.1
Ray, T.A.2
Florijn, R.3
-
16
-
-
84856867776
-
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness
-
I. Audo, K. Bujakowska, E. Orhan Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness Am J Hum Genet 90 2 2012 321 330
-
(2012)
Am J Hum Genet
, vol.90
, Issue.2
, pp. 321-330
-
-
Audo, I.1
Bujakowska, K.2
Orhan, E.3
-
17
-
-
0041104621
-
1- subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness
-
DOI 10.1038/947
-
N.T. Bech-Hansen, M.J. Naylor, T.A. Maybaum Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness Nat Genet 19 3 1998 264 267 (Pubitemid 28309339)
-
(1998)
Nature Genetics
, vol.19
, Issue.3
, pp. 264-267
-
-
Torben Bech-Hansen, N.1
Naylor, M.J.2
Maybaum, T.A.3
Pearce, W.G.4
Koop, B.5
Fishman, G.A.6
Mets, M.7
Musarella, M.A.8
Boycott, K.M.9
-
18
-
-
0033744810
-
Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F
-
K.M. Boycott, W.G. Pearce, N.T. Bech-Hansen Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F Can J Ophthalmol 35 4 2000 204 213
-
(2000)
Can J Ophthalmol
, vol.35
, Issue.4
, pp. 204-213
-
-
Boycott, K.M.1
Pearce, W.G.2
Bech-Hansen, N.T.3
-
19
-
-
33749005104
-
2+-binding protein 4, cause autosomal recessive night blindness
-
DOI 10.1086/508067
-
C. Zeitz, B. Kloeckener-Gruissem, U. Forster Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness Am J Hum Genet 79 4 2006 657 667 (Pubitemid 44452743)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.4
, pp. 657-667
-
-
Zeitz, C.1
Kloeckener-Gruissem, B.2
Forster, U.3
Kohl, S.4
Magyar, I.5
Wissinger, B.6
Matyas, G.7
Borruat, F.-X.8
Schorderet, D.F.9
Zrenner, E.10
Munier, F.L.11
Berger, W.12
-
20
-
-
33751110923
-
Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy
-
DOI 10.1086/508944
-
K.A. Wycisk, C. Zeitz, S. Feil Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy Am J Hum Genet 79 5 2006 973 977 (Pubitemid 44763412)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.5
, pp. 973-977
-
-
Wycisk, K.A.1
Zeitz, C.2
Feil, S.3
Wittmer, M.4
Forster, U.5
Neidhardt, J.6
Wissinger, B.7
Zrenner, E.8
Wilke, R.9
Kohl, S.10
Berger, W.11
-
21
-
-
72149100295
-
Genotyping microarray for CSNB-associated genes
-
C. Zeitz, S. Labs, B. Lorenz Genotyping microarray for CSNB-associated genes Invest Ophthalmol Vis Sci 50 12 2009 5919 5926
-
(2009)
Invest Ophthalmol Vis Sci
, vol.50
, Issue.12
, pp. 5919-5926
-
-
Zeitz, C.1
Labs, S.2
Lorenz, B.3
-
22
-
-
0033744611
-
Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson memorial lecture
-
T.P. Dryja Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson memorial lecture Am J Ophthalmol 130 5 2000 547 563
-
(2000)
Am J Ophthalmol
, vol.130
, Issue.5
, pp. 547-563
-
-
Dryja, T.P.1
-
23
-
-
66749117504
-
Molecular genetics and protein function involved in nocturnal vision
-
C. Zeitz Molecular genetics and protein function involved in nocturnal vision Expert Rev Ophthalmol 2 3 2007 467 485
-
(2007)
Expert Rev Ophthalmol
, vol.2
, Issue.3
, pp. 467-485
-
-
Zeitz, C.1
-
24
-
-
84855921203
-
Congenital stationary night blindness: Mutation update and clinical variability
-
N. Lodha, C.M. Loucks, C. Beaulieu, J.S. Parboosingh, N.T. Bech-Hansen Congenital stationary night blindness: mutation update and clinical variability Adv Exp Med Biol 723 5 2012 371 379
-
(2012)
Adv Exp Med Biol
, vol.723
, Issue.5
, pp. 371-379
-
-
Lodha, N.1
Loucks, C.M.2
Beaulieu, C.3
Parboosingh, J.S.4
Bech-Hansen, N.T.5
-
25
-
-
0010548410
-
Über eine Abart von Hemeralopie
-
C. Oguchi Über eine Abart von Hemeralopie Acta Soc Ophthalmol Jpn 11 1907 123 134
-
(1907)
Acta Soc Ophthalmol Jpn
, vol.11
, pp. 123-134
-
-
Oguchi, C.1
-
26
-
-
78650848731
-
On a new discovery in the dark adaptation of Oguchi's disease
-
G. Mizuo On a new discovery in the dark adaptation of Oguchi's disease Acta Soc Ophthalmol Jpn 17 1913 1854 1859
-
(1913)
Acta Soc Ophthalmol Jpn
, vol.17
, pp. 1854-1859
-
-
Mizuo, G.1
-
27
-
-
0031038950
-
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness
-
DOI 10.1038/ng0297-175
-
S. Yamamoto, K.C. Sippel, E.L. Berson, T.P. Dryja Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness Nat Genet 15 2 1997 175 178 (Pubitemid 27061637)
-
(1997)
Nature Genetics
, vol.15
, Issue.2
, pp. 175-178
-
-
Yamamoto, S.1
Sippel, K.C.2
Berson, E.L.3
Dryja, T.P.4
-
28
-
-
0029067542
-
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese
-
S. Fuchs, M. Nakazawa, M.A. Maw, M. Tamai, Y. Oguchi, A. Gal A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese Nat Genet 10 3 1995 360 362
-
(1995)
Nat Genet
, vol.10
, Issue.3
, pp. 360-362
-
-
Fuchs, S.1
Nakazawa, M.2
Maw, M.A.3
Tamai, M.4
Oguchi, Y.5
Gal, A.6
-
29
-
-
0031762898
-
A naturally occurring mouse model of X-linked congenital stationary night blindness
-
M.T. Pardue, M.A. McCall, M.M. LaVail, R.G. Gregg, N.S. Peachey A naturally occurring mouse model of X-linked congenital stationary night blindness Invest Ophthalmol Vis Sci 39 12 1998 2443 2449 (Pubitemid 28485655)
-
(1998)
Investigative Ophthalmology and Visual Science
, vol.39
, Issue.12
, pp. 2443-2449
-
-
Pardue, M.T.1
McCall, M.A.2
LaVail, M.M.3
Gregg, R.G.4
Peachey, N.S.5
-
30
-
-
0033616582
-
Abnormal photoresponses and light-induced apoptosis in rods lacking rhodopsin kinase
-
DOI 10.1073/pnas.96.7.3718
-
C.K. Chen, M.E. Burns, M. Spencer Abnormal photoresponses and light-induced apoptosis in rods lacking rhodopsin kinase Proc Natl Acad Sci U S A 96 7 1999 3718 3722 (Pubitemid 29168976)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.7
, pp. 3718-3722
-
-
Chen, C.-K.1
Burns, M.E.2
Spencer, M.3
Niemi, G.A.4
Chen, J.5
Hurley, J.B.6
Baylor, D.A.7
Simon, M.I.8
-
31
-
-
51849092643
-
Comparisons of structural and functional abnormalities in mouse b-wave mutants
-
M.A. McCall, R.G. Gregg Comparisons of structural and functional abnormalities in mouse b-wave mutants J Physiol 586 18 2008 4385 4392
-
(2008)
J Physiol
, vol.586
, Issue.18
, pp. 4385-4392
-
-
McCall, M.A.1
Gregg, R.G.2
-
32
-
-
0018137595
-
Correlation of clinicopathologic findings in a patient. Congenital night blindness, branch retinal vein occlusion, cilioretinal artery, drusen of the optic nerve head, and intraretinal pigmented lesion
-
H.A. Vaghefi, W.R. Green, J.S. Kelley, L.L. Sloan, R.E. Hoover, A. Patz Correlation of clinicopathologic findings in a patient: congenital night blindness, branch retinal vein occlusion, cilioretinal artery, drusen of the optic nerve head, and intraretinal pigmented lesion Arch Ophthalmol 96 11 1978 2097 2104 (Pubitemid 9008440)
-
(1978)
Archives of Ophthalmology
, vol.96
, Issue.11
, pp. 2097-2104
-
-
Vaghefi, H.A.1
Green, W.R.2
Kelley, J.S.3
-
33
-
-
0023021422
-
Congenital stationary night blindness with myopia: A clinico-pathologic study
-
I. Watanabe, Y. Taniguchi, K. Morioka, M. Kato Congenital stationary night blindness with myopia: a clinico-pathologic study Doc Ophthalmol 63 1 1986 55 62 (Pubitemid 16091999)
-
(1986)
Documenta Ophthalmologica
, vol.63
, Issue.1
, pp. 55-62
-
-
Watanabe, I.1
Taniguchi, Y.2
Morioka, K.3
Kato, M.4
-
34
-
-
83555162617
-
Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosa
-
R.W.S. Chen, J.P. Greenberg, M.A. Lazow Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosa Am J Ophthalmol 153 1 2011 143 154
-
(2011)
Am J Ophthalmol
, vol.153
, Issue.1
, pp. 143-154
-
-
Chen, R.W.S.1
Greenberg, J.P.2
Lazow, M.A.3
-
35
-
-
0033800554
-
Mizuo phenomenon observed by scanning laser ophthalmoscopy in a patient with Oguchi disease
-
T. Usui, M. Ichibe, S. Ueki Mizuo phenomenon observed by scanning laser ophthalmoscopy in a patient with Oguchi disease Am J Ophthalmol 130 3 2000 359 361
-
(2000)
Am J Ophthalmol
, vol.130
, Issue.3
, pp. 359-361
-
-
Usui, T.1
Ichibe, M.2
Ueki, S.3
-
36
-
-
8044222417
-
Histopathological and electron microscopic studies on the retina of Oguchi's disease (article in Japanese)
-
Y. Kuwabara, K. Ishihara, S. Akiya Histopathological and electron microscopic studies on the retina of Oguchi's disease (article in Japanese) Acta Soc Ophthalmol Jpn 67 1963 1323 1351
-
(1963)
Acta Soc Ophthalmol Jpn
, vol.67
, pp. 1323-1351
-
-
Kuwabara, Y.1
Ishihara, K.2
Akiya, S.3
-
37
-
-
70349859876
-
Shortening of the rod outer segment in Oguchi disease
-
H. Hashimoto, S. Kishi Shortening of the rod outer segment in Oguchi disease Graefes Arch Clin Exp Ophthalmol 247 11 2009 1561 1563
-
(2009)
Graefes Arch Clin Exp Ophthalmol
, vol.247
, Issue.11
, pp. 1561-1563
-
-
Hashimoto, H.1
Kishi, S.2
-
38
-
-
79952293819
-
Spectral-domain optical coherence tomography findings in the Mizuo-Nakamura phenomenon of Oguchi Disease
-
M. Takada, A. Otani, K. Ogino, N. Yoshimura Spectral-domain optical coherence tomography findings in the Mizuo-Nakamura phenomenon of Oguchi Disease Retina 31 3 2011 626 628
-
(2011)
Retina
, vol.31
, Issue.3
, pp. 626-628
-
-
Takada, M.1
Otani, A.2
Ogino, K.3
Yoshimura, N.4
-
39
-
-
79953059275
-
Macular dysfunction in Oguchi disease with the frequent mutation 1147delA in the SAG gene
-
T. Hayashi, S. Tsuzuranuki, K. Kozaki, M. Urashima, H. Tsuneoka Macular dysfunction in Oguchi disease with the frequent mutation 1147delA in the SAG gene Ophthalmic Res 46 4 2011 175 180
-
(2011)
Ophthalmic Res
, vol.46
, Issue.4
, pp. 175-180
-
-
Hayashi, T.1
Tsuzuranuki, S.2
Kozaki, K.3
Urashima, M.4
Tsuneoka, H.5
-
40
-
-
77749255403
-
Optical coherence tomographic evaluation of the outer retinal architecture in Oguchi Disease
-
K. Yamada, Y. Motomura, C.S. Matsumoto, K. Shinoda, K. Nakatsuka Optical coherence tomographic evaluation of the outer retinal architecture in Oguchi Disease Jpn J Ophthalmol 53 5 2009 449 451
-
(2009)
Jpn J Ophthalmol
, vol.53
, Issue.5
, pp. 449-451
-
-
Yamada, K.1
Motomura, Y.2
Matsumoto, C.S.3
Shinoda, K.4
Nakatsuka, K.5
-
41
-
-
80051741669
-
Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG gene
-
1098-1011
-
P.I. Sergouniotis, A.E. Davidson, K. Sehmi, A.R. Webster, A.G. Robson, A.T. Moore Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG gene Eye 25 8 2011 1098-1011
-
(2011)
Eye
, vol.25
, Issue.8
-
-
Sergouniotis, P.I.1
Davidson, A.E.2
Sehmi, K.3
Webster, A.R.4
Robson, A.G.5
Moore, A.T.6
-
42
-
-
84860484870
-
A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene
-
P.I. Sergouniotis, A.G. Robson, Z. Li A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene Acta Ophthalmol 90 3 2012 192 197
-
(2012)
Acta Ophthalmol
, vol.90
, Issue.3
, pp. 192-197
-
-
Sergouniotis, P.I.1
Robson, A.G.2
Li, Z.3
-
43
-
-
77949526841
-
Retinal imaging using commercial broadband optical coherence tomography
-
H. Tanna, A.M. Dubis, N. Ayub Retinal imaging using commercial broadband optical coherence tomography Br J Ophthalmol 94 3 2010 372 376
-
(2010)
Br J Ophthalmol
, vol.94
, Issue.3
, pp. 372-376
-
-
Tanna, H.1
Dubis, A.M.2
Ayub, N.3
-
44
-
-
80052496334
-
Anatomical correlates to the bands seen in the outer retina by optical coherence tomography: Literature review and model
-
R.F. Spaide, C.A. Curcio Anatomical correlates to the bands seen in the outer retina by optical coherence tomography: literature review and model Retina 31 8 2011 1609 1619
-
(2011)
Retina
, vol.31
, Issue.8
, pp. 1609-1619
-
-
Spaide, R.F.1
Curcio, C.A.2
-
45
-
-
73949111344
-
Cone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsin
-
J. Carroll, R.C. Baraas, M. Wagner-Schuman Cone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsin Proc Natl Acad Sci U S A 106 49 2009 20948 20953
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, Issue.49
, pp. 20948-20953
-
-
Carroll, J.1
Baraas, R.C.2
Wagner-Schuman, M.3
-
46
-
-
0031732523
-
Relation of optical coherence tomography to microanatomy in normal and rd chickens
-
Y. Huang, A.V. Cideciyan, G.I. Papastergiou Relation of optical coherence tomography to microanatomy in normal and rd chickens Invest Ophthalmol Vis Sci 39 12 1998 2405 2416 (Pubitemid 28485652)
-
(1998)
Investigative Ophthalmology and Visual Science
, vol.39
, Issue.12
, pp. 2405-2416
-
-
Huang, Y.1
Cideciyan, A.V.2
Papastergiou, G.I.3
Banin, E.4
Semple-Rowland, S.L.5
Milam, A.H.6
Jacobson, S.G.7
-
47
-
-
77950517860
-
Arrested development: High-resolution imaging of foveal morphology in albinism
-
J.T. McAllister, A.M. Dubis, D.M. Tait Arrested development: high-resolution imaging of foveal morphology in albinism Vision Res 50 8 2010 810 817
-
(2010)
Vision Res
, vol.50
, Issue.8
, pp. 810-817
-
-
McAllister, J.T.1
Dubis, A.M.2
Tait, D.M.3
-
48
-
-
84861095948
-
Spatial and temporal variation of rod photoreceptor reflectance in the human retina
-
R.F. Cooper, A.M. Dubis, A. Pavaskar, J. Rha, A. Dubra, J. Carroll Spatial and temporal variation of rod photoreceptor reflectance in the human retina Biomed Opt Express 2 9 2011 2577 2589
-
(2011)
Biomed Opt Express
, vol.2
, Issue.9
, pp. 2577-2589
-
-
Cooper, R.F.1
Dubis, A.M.2
Pavaskar, A.3
Rha, J.4
Dubra, A.5
Carroll, J.6
-
49
-
-
84857609754
-
Reflective afocal broadband adaptive optics scanning ophthalmoscope
-
A. Dubra, Y. Sulai Reflective afocal broadband adaptive optics scanning ophthalmoscope Biomed Opt Express 2 6 2011 1757 1768
-
(2011)
Biomed Opt Express
, vol.2
, Issue.6
, pp. 1757-1768
-
-
Dubra, A.1
Sulai, Y.2
-
50
-
-
82255164373
-
Non-invasive imaging of the human rod photoreceptor mosaic using a confocal adaptive optics scanning ophthalmoscope
-
A. Dubra, Y. Sulai, J.L. Norris Non-invasive imaging of the human rod photoreceptor mosaic using a confocal adaptive optics scanning ophthalmoscope Biomed Opt Express 2 7 2011 1864 1876
-
(2011)
Biomed Opt Express
, vol.2
, Issue.7
, pp. 1864-1876
-
-
Dubra, A.1
Sulai, Y.2
Norris, J.L.3
-
51
-
-
77955320503
-
Registration of 2D images from fast scanning ophthalmic instruments
-
Springer Heidelberg
-
A. Dubra, Z. Harvey Registration of 2D images from fast scanning ophthalmic instruments Biomedical Image Registration Vol 6204 2010 Springer Heidelberg 60 71
-
(2010)
Biomedical Image Registration
, vol.6204
, pp. 60-71
-
-
Dubra, A.1
Harvey, Z.2
-
53
-
-
84861102023
-
Repeatability of in vivo parafoveal cone density and spacing measurements
-
R. Garrioch, C. Langlo, A.M. Dubis, R.F. Cooper, A. Dubra, J. Carroll Repeatability of in vivo parafoveal cone density and spacing measurements Optometry Vision Sci 89 5 2012 632 643
-
(2012)
Optometry Vision Sci
, vol.89
, Issue.5
, pp. 632-643
-
-
Garrioch, R.1
Langlo, C.2
Dubis, A.M.3
Cooper, R.F.4
Dubra, A.5
Carroll, J.6
-
54
-
-
0025014937
-
Human photoreceptor topography
-
C.A. Curcio, K.R. Sloan, R.E. Kalina, A.E. Hendrickson Human photoreceptor topography J Comp Neurol 292 4 1990 497 523 (Pubitemid 20076633)
-
(1990)
Journal of Comparative Neurology
, vol.292
, Issue.4
, pp. 497-523
-
-
Curcio, C.A.1
Sloan, K.R.2
Kalina, R.E.3
Hendrickson, A.E.4
-
56
-
-
84856144794
-
Temporal changes of human cone photoreceptors observed in vivo with SLO/OCT
-
M. Pircher, J.S. Kroisamer, F. Felberer, H. Sattmann, E. Götzinger, C.K. Hitzenberger Temporal changes of human cone photoreceptors observed in vivo with SLO/OCT Biomed Opt Express 2 1 2010 100 112
-
(2010)
Biomed Opt Express
, vol.2
, Issue.1
, pp. 100-112
-
-
Pircher, M.1
Kroisamer, J.S.2
Felberer, F.3
Sattmann, H.4
Götzinger, E.5
Hitzenberger, C.K.6
-
57
-
-
33646560306
-
Adaptive optics flood-illumination camera for high speed retinal imaging
-
DOI 10.1364/OE.14.004552
-
J. Rha, R.S. Jonnal, K.E. Thorn, J. Qu, Y. Zhang, D.T. Miller Adaptive optics flood-illumination camera for high speed retinal imaging Opt Express 14 10 2006 4552 4569 (Pubitemid 43727645)
-
(2006)
Optics Express
, vol.14
, Issue.10
, pp. 4552-4569
-
-
Rha, J.1
Jonnal, R.S.2
Thorn, K.E.3
Qu, J.4
Zhang, Y.5
Miller, D.T.6
-
58
-
-
77749315043
-
Imaging outer segment renewal in living human cone photoreceptors
-
R.S. Jonnal, J.R. Besecker, J.C. Derby Imaging outer segment renewal in living human cone photoreceptors Opt Express 18 5 2010 5257 5270
-
(2010)
Opt Express
, vol.18
, Issue.5
, pp. 5257-5270
-
-
Jonnal, R.S.1
Besecker, J.R.2
Derby, J.C.3
-
59
-
-
0035576022
-
Species-specific differences in expression of G-protein-coupled receptor kinase (GRK) 7 and GRK1 in mammalian cone photoreceptor cells: Implications for cone cell phototransduction
-
E.R. Weiss, M.H. Ducceschi, T.J. Horner, A. Li, C.M. Craft, S. Osawa Species-specific differences in expression of G-protein-coupled receptor kinase (GRK) 7 and GRK1 in mammalian cone photoreceptor cells: implications for cone cell phototransduction J Neurosci 21 23 2001 9175 9184 (Pubitemid 33096861)
-
(2001)
Journal of Neuroscience
, vol.21
, Issue.23
, pp. 9175-9184
-
-
Weiss, E.R.1
Ducceschi, M.H.2
Horner, T.J.3
Li, A.4
Craft, C.M.5
Osawa, S.6
-
61
-
-
36749089929
-
In vivo functional imaging of human cone photoreceptors
-
DOI 10.1364/OE.15.016141
-
R.S. Jonnal, J. Rha, Y. Zhang, B. Cense, W. Gao, D.T. Miller In vivo functional imaging of human cone photoreceptors Opt Express 14 24 2007 16141 16160 (Pubitemid 350214428)
-
(2007)
Optics Express
, vol.15
, Issue.24
, pp. 16141-16160
-
-
Jonnal, R.S.1
Rha, J.2
Zhang, Y.3
Cense, B.4
Gao, W.5
Miller, D.T.6
-
62
-
-
40649115751
-
Intrinsic signals from human cone photoreceptors
-
K. Grieve, A. Roorda Intrinsic signals from human cone photoreceptors Invest Ophthalmol Vis Sci 49 2 2008 713 719
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, Issue.2
, pp. 713-719
-
-
Grieve, K.1
Roorda, A.2
-
63
-
-
72649102474
-
Variable optical activation of human cone photoreceptors visualized using short coherence light source
-
J. Rha, B. Schroeder, P. Godara, J. Carroll Variable optical activation of human cone photoreceptors visualized using short coherence light source Opt Lett 34 24 2009 3782 3784
-
(2009)
Opt Lett
, vol.34
, Issue.24
, pp. 3782-3784
-
-
Rha, J.1
Schroeder, B.2
Godara, P.3
Carroll, J.4
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