-
1
-
-
0031914254
-
Keratoconus
-
DOI 10.1016/S0039-6257(97)00119-7, PII S0039625797001197
-
Rabinowitz YS. Keratoconus. Surv Ophthalmol 1998;42:297-319. (Pubitemid 28092771)
-
(1998)
Survey of Ophthalmology
, vol.42
, Issue.4
, pp. 297-319
-
-
Rabinowitz, Y.S.1
-
2
-
-
35148818718
-
Longitudinal study of keratoconus progression
-
DOI 10.1016/j.exer.2007.06.016, PII S0014483507001741
-
Li X, Yang H, Rabinowitz YS. Longitudinal study of keratoconus progression. Exp Eye Res 2007;85:502-7. (Pubitemid 47534204)
-
(2007)
Experimental Eye Research
, vol.85
, Issue.4
, pp. 502-507
-
-
Li, X.1
Yang, H.2
Rabinowitz, Y.S.3
-
3
-
-
0022509824
-
Clinical and epidemiological features of keratoconus: Genetic and external factors in the pathogenesis of the disease
-
Ihalainen A. Clinical and epidemiological features of keratoconus: genetic and external factors in the pathogenesis of the disease. Acta Ophthalmol 1986;178:1-64.
-
(1986)
Acta Ophthalmol
, vol.178
, pp. 1-64
-
-
Ihalainen, A.1
-
5
-
-
0021990977
-
Prevalence of keratoconus patients in Japan
-
Tanabe U, Fujiki K, Ogawa A, Ueda S, Kanai A. Prevalence of keratoconus patients in Japan. Nippon Ganka Gakkai Zasshi 1985;89:407-11. (Pubitemid 15106122)
-
(1985)
Journal of Japanese Ophthalmological Society
, vol.89
, Issue.3
, pp. 407-411
-
-
Tanabe, U.1
Fujiki, K.2
Ogawa, A.3
-
6
-
-
2342637192
-
Influence of ethnic origin on the incidence of keratoconus and associated atopic disease in Asians and white patients
-
DOI 10.1038/sj.eye.6700652
-
Georgiou T, Funnell CL, Cassels-Brown A, OConor R. Influence of ethnic origin on the incidence of keratoconus and associated atopic disease in Asians and white patients. Eye 2004;18:379-83. (Pubitemid 38585012)
-
(2004)
Eye
, vol.18
, Issue.4
, pp. 379-383
-
-
Georgiou, T.1
Funnell, C.L.2
Cassels-Brown, A.3
O'Conor, R.4
-
7
-
-
0042881041
-
Mathematical multi-locus approaches to localizing complex human trait genes
-
DOI 10.1038/nrg1155
-
Hoh J, Ott J. Mathematical multi-locus approaches to localizing complex human traits genes. Nat Rev Genet 2003;4:701-9. (Pubitemid 37046137)
-
(2003)
Nature Reviews Genetics
, vol.4
, Issue.9
, pp. 701-709
-
-
Hoh, J.1
Ott, J.2
-
8
-
-
29744449083
-
Estimation of the incidence and factors predictive of corneal scarring in the Collaborative Longitudinal Evaluation of Keratoconus (CLEK) study
-
DOI 10.1097/01.ico.0000164831.87593.08
-
Barr JT, Wilson BS, Gordon MO, Rah MJ, Riley C, Kollbaum PS, et al. Estimation of the incidence and factors predictive of corneal scarring in the Collaborative Longitudinal Evaluation of Keratoconus (CLEK) Study. Cornea 2006;25:16-25. (Pubitemid 43031143)
-
(2006)
Cornea
, vol.25
, Issue.1
, pp. 16-25
-
-
Barr, J.T.1
Wilson, B.S.2
Gordon, M.O.3
Rah, M.J.4
Riley, C.5
Kollbaum, P.S.6
Zadnik, K.7
-
9
-
-
3342998335
-
Asymmetric keratoconus attributed to eye rubbing
-
DOI 10.1097/01.ico.0000121711.58571.8d
-
Jafri B, Lichter H, Stulting RD. Asymmetric keratoconus attributed to eye rubbing. Cornea 2004;23:560-4. (Pubitemid 38988695)
-
(2004)
Cornea
, vol.23
, Issue.6
, pp. 560-564
-
-
Jafri, B.1
Lichter, H.2
Stulting, R.D.3
-
10
-
-
77953556702
-
Mutational screening of VSX1 in keratoconus patients from the European population
-
Dash DP, George S, OPrey D, Burns D, Nabili S, Donnelly U, et al. Mutational screening of VSX1 in keratoconus patients from the European population. Eye (Lond) 2010;24:1085-92.
-
(2010)
Eye (Lond)
, vol.24
, pp. 1085-1092
-
-
Dash, D.P.1
George, S.2
Oprey, D.3
Burns, D.4
Nabili, S.5
Donnelly, U.6
-
11
-
-
1542616280
-
A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13
-
Brancati F, Valente EM, Sarkozy A, Fehèr J, Castori M, Del Duca P, et al. A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13. J Med Genet 2004;41:188-92.
-
(2004)
J Med Genet
, vol.41
, pp. 188-192
-
-
Brancati, F.V.1
-
12
-
-
64049099287
-
Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32
-
Gajecka M, Radhakrishna U, Winters D, Nath SK, Rydzanicz M, Ratnamala U, et al. Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32. Invest Ophthalmol Vis Sci 2009;50:1531-9.
-
(2009)
Invest Ophthalmol Vis Sci
, vol.50
, pp. 1531-1539
-
-
Gajecka, M.1
Radhakrishna, U.2
Winters, D.3
Nath, S.K.4
Rydzanicz, M.5
Ratnamala, U.6
-
13
-
-
19944430943
-
Identification of a new locus for isolated familial keratoconus at 2p24
-
Hutchings H, Ginisty H, Le Gallo M, Levy D, Stoësser F, Rouland JF, et al. Identification of a new locus for isolated familial keratoconus at 2p24. J Med Genet 2005;42:88-94.
-
(2005)
J Med Genet
, vol.42
, pp. 88-94
-
-
Hutchings, H.G.1
-
14
-
-
62649139163
-
Linkage analysis in keratoconus: Replication of locus 5q21.2 and identification of other suggestive Loci
-
Bisceglia L, De Bonis P, Pizzicoli C, Fischetti L, Laborante A, Di Perna M, et al. Linkage analysis in keratoconus: replication of locus 5q21.2 and identification of other suggestive Loci. Invest Ophthalmol Vis Sci 2009;50:1081-6.
-
(2009)
Invest Ophthalmol Vis Sci
, vol.50
, pp. 1081-1086
-
-
Bisceglia, L.1
De Bonis, P.2
Pizzicoli, C.3
Fischetti, L.4
Laborante, A.5
Di Perna, M.6
-
15
-
-
84874234154
-
A Genome-Wide Association Scan for Keratoconus Identifies Novel Candidate Genes
-
Poster #4646
-
Burdon KP, Laurie KJ, Mills RA, Coster DJ, MacGregor S, Craig JE. A Genome-Wide Association Scan for Keratoconus Identifies Novel Candidate Genes. ARVO 2010. Poster #4646.
-
(2010)
ARVO
-
-
Burdon, K.P.1
Laurie, K.J.2
Mills, R.A.3
Coster, D.J.4
MacGregor, S.5
Craig, J.E.6
-
16
-
-
0036590069
-
Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia
-
DOI 10.1007/s00439-002-0705-7
-
Fullerton J, Paprocki P, Foote S, Mackey DA, Williamson R, Forrest S. Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia. Hum Genet 2002;110:462-70. (Pubitemid 36074992)
-
(2002)
Human Genetics
, vol.110
, Issue.5
, pp. 462-470
-
-
Fullerton, J.1
Paprocki, P.2
Foote, S.3
Mackey, D.A.4
Williamson, R.5
Forrest, S.6
-
17
-
-
23744433964
-
Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1
-
DOI 10.1097/01.GIM.0000170772.41860.54
-
Tang YG, Rabinowitz YS, Taylor KD, Li X, Hu M, Picornell Y, et al. Genome wide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome5q14.3-q21.1. Genet Med 2005;7:397-405. (Pubitemid 41139623)
-
(2005)
Genetics in Medicine
, vol.7
, Issue.6
, pp. 397-405
-
-
Tang, Y.G.1
Rabinowitz, Y.S.2
Taylor, K.D.3
Li, X.4
Hu, M.5
Picornell, Y.6
Yang, H.7
-
18
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
DOI 10.1038/35015718
-
Risch NJ. Searching for genetic determinants in the new millennium. Nature 2000;405:847-56. (Pubitemid 30407863)
-
(2000)
Nature
, vol.405
, Issue.6788
, pp. 847-856
-
-
Risch, N.J.1
-
19
-
-
55749116326
-
Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci
-
Burdon KP, Coster DJ, Charlesworth JC, Mills RA, Laurie KJ, Giunta C, et al. Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci. Hum Genet 2008;124:379-86.
-
(2008)
Hum Genet
, vol.124
, pp. 379-86
-
-
Burdon, K.P.1
Coster, D.J.2
Charlesworth, J.C.3
Mills, R.A.4
Laurie, K.J.5
Giunta, C.6
-
20
-
-
57649200165
-
Association of -31T>C and -511 C>T polymorphisms in the interleukin 1 beta (IL1B) promoter in Korean keratoconus patients
-
Kim SH, Mok JW, Kim HS, Joo CK. Association of -31T>C and -511 C>T polymorphisms in the interleukin 1 beta (IL1B) promoter in Korean keratoconus patients. Mol Vis 2008;14:2109-16.
-
(2008)
Mol Vis
, vol.14
, pp. 2109-16
-
-
Kim, S.H.1
Mok, J.W.2
Kim, H.S.3
Joo, C.K.4
-
21
-
-
0034758045
-
Genomewide scans of complex human diseases: True linkage is hard to find
-
DOI 10.1086/324069
-
Altmüller J, Palmer LJ, Fischer G, Scherb H, Wjst M. Genomewide scans of complex human diseases: true linkage is hard to find. Am J Hum Genet 2001;69:936-50. (Pubitemid 33015809)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.5
, pp. 936-950
-
-
Altmuller, J.1
Palmer, L.J.2
Fischer, G.3
Scherb, H.4
Wjst, M.5
-
22
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K. The future of genetic studies of complex human diseases. Science 1996;273:1516-7. (Pubitemid 26301653)
-
(1996)
Science
, vol.273
, Issue.5281
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
23
-
-
42649123990
-
Sizing up human height variation
-
DOI 10.1038/ng0508-489, PII NG0508489
-
Visscher PM. Sizing up human height variation. Nat Genet 2008;40:489-90. (Pubitemid 351601227)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, pp. 489-490
-
-
Visscher, P.M.1
-
24
-
-
4344587901
-
Linkage analysis of the genetic loci for high myopia on 18p, 12q, and 17q in 51 U.K. families
-
DOI 10.1167/iovs.03-1156
-
Farbrother JE, Kirov G, Owen MJ, Pong-Wong R, Haley CS, Guggenheim JA. Linkage analysis of the genetic loci for high myopia on 18p, 12q, and 17q in 51 U.K. families. Invest Ophthalmol Vis Sci 2004;45:2879-85. (Pubitemid 39121813)
-
(2004)
Investigative Ophthalmology and Visual Science
, vol.45
, Issue.9
, pp. 2879-2885
-
-
Farbrother, J.E.1
Kirov, G.2
Owen, M.J.3
Pong-Wong, R.4
Haley, C.S.5
Guggenheim, J.A.6
-
25
-
-
50549101770
-
Topographic evaluation of relatives of patients with keratoconus
-
Karimian F, Aramesh S, Rabei HM, Javadi MA, Rafati N. Topographic evaluation of relatives of patients with keratoconus. Cornea 2008;27:874-8.
-
(2008)
Cornea
, vol.27
, pp. 874-8
-
-
Karimian, F.1
Aramesh, S.2
Rabei, H.M.3
Ma, J.4
Rafati, N.5
-
26
-
-
48249105538
-
Evaluation of corneal topography with Orbscan II in first-degree relatives of patients with keratoconus
-
Kaya V, Utine CA, Altunsoy M, Oral D, Yilmaz OF. Evaluation of corneal topography with Orbscan II in first-degree relatives of patients with keratoconus. Cornea 2008;27:531-4.
-
(2008)
Cornea
, vol.27
, pp. 531-4
-
-
Kaya, V.1
Utine, C.A.2
Altunsoy, M.3
Oral, D.4
Yilmaz, O.F.5
-
27
-
-
0345714659
-
Familial keratoconus with cataract: Linkage to the long arm of chromosome 15 and exclusion of candidate genes
-
DOI 10.1167/iovs.03-0399
-
Hughes AE, Dash DP, Jackson AJ, Frazer DG, Silvestri G. Familial keratoconus with cataract: linkage to the long arm of chromosome and exclusion of candidate genes. Invest Ophthalmol Vis Sci 2003;44:5063-6. (Pubitemid 37475371)
-
(2003)
Investigative Ophthalmology and Visual Science
, vol.44
, Issue.12
, pp. 5063-5066
-
-
Hughes, A.E.1
Dash, D.P.2
Jackson, A.J.3
Frazer, D.G.4
Silvestri, G.5
-
29
-
-
17644369618
-
Mental retardation, keratoconus, febrile seizures and sinoatrial block: A previously undescribed autosomal recessive disorder [6]
-
DOI 10.1111/j.1399-0004.2005.00429.x
-
Kirby D, Jackson AP, Karbani G, Crow YJ. Mental retardation, keratoconus, febrile seizures and sinoatrial block: a previously undescribed autosomal recessive disorder. Clin Genet 2005;67:448-9. (Pubitemid 40561500)
-
(2005)
Clinical Genetics
, vol.67
, Issue.5
, pp. 448-449
-
-
Kirby, D.1
Jackson, A.P.2
Karbani, G.3
Crow, Y.J.4
-
31
-
-
0036784886
-
A locus for autosomal dominant keratoconus: Linkage to 16q22.3-q23.1 in Finnish families
-
Tyynismaa H, Sistonen P, Tuupanen S, Tervo T, Dammert A, Latvala T, et al. A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families. Invest Ophthalmol Vis Sci 2002;43:3160-4.
-
(2002)
Invest Ophthalmol Vis Sci
, vol.43
, pp. 3160-4
-
-
Tyynismaa, H.1
Sistonen, P.2
Tuupanen, S.3
Tervo, T.4
Dammert, A.5
Latvala, T.6
-
32
-
-
0036566556
-
VSX1: A gene for posterior polymorphous dystrophy and keratoconus
-
Héon E, Greenberg A, Kopp KK, Rootman D, Vincent AL, Billingsley G, et al. VSX1: a gene for posterior polymorphous dystrophy and keratoconus. Hum Mol Genet 2002;11:1029-36.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1029-36
-
-
Héon, E.G.1
-
33
-
-
0034097372
-
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13
-
Hameed A, Khaliq S, Ismail M, Anwar K, Ebenezer ND, Jordan T, et al. A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13. Invest Ophthalmol Vis Sci 2000;41:629-33. (Pubitemid 30158869)
-
(2000)
Investigative Ophthalmology and Visual Science
, vol.41
, Issue.3
, pp. 629-633
-
-
Hameed, A.1
Khaliq, S.2
Ismail, M.3
Anwar, K.4
Ebenezer, N.D.5
Jordan, T.6
Mehdi, S.Q.7
Payne, A.M.8
Bhattacharya, S.S.9
-
34
-
-
33749149463
-
Two-stage genome-wide linkage scan in keratoconus sib pair families
-
DOI 10.1167/iovs.06-0214
-
Li X, Rabinowitz YS, Tang YG, Picornell Y, Taylor KD, Hu M, et al. Two-stage genome-wide linkage scan in keratoconus sib pair families. Invest Ophthalmol Vis Sci 2006;47:3791-5. (Pubitemid 46044293)
-
(2006)
Investigative Ophthalmology and Visual Science
, vol.47
, Issue.9
, pp. 3791-3795
-
-
Li, X.1
Rabinowitz, Y.S.2
Tang, Y.G.3
Picornell, Y.4
Taylor, K.D.5
Hu, M.6
Yang, H.7
-
35
-
-
77957015775
-
Evidence for keratoconus susceptibility locus on chromosome 14: A genome-wide linkage screen using single-nucleotide polymorphism markers
-
Liskova P, Hysi PG, Waseem N, Ebenezer ND, Bhattacharya SS, Tuft SJ. Evidence for keratoconus susceptibility locus on chromosome 14: a genome-wide linkage screen using single-nucleotide polymorphism markers. Arch Ophthalmol 2010;128:1191-5.
-
(2010)
Arch Ophthalmol
, vol.128
, pp. 1191-5
-
-
Liskova, P.1
Hysi, P.G.2
Waseem, N.3
Ebenezer, N.D.4
Bhattacharya, S.S.5
Tuft, S.J.6
-
36
-
-
33746705124
-
No VSX1 gene mutations associated with keratoconus
-
DOI 10.1167/iovs.05-1530
-
Aldave AJ, Yellore VS, Salem AK, Yoo GL, Rayner SA, Yang H, et al. No VSX1 gene mutations associated with keratoconus. Invest Ophthalmol Vis Sci 2006;47:2820-2. (Pubitemid 351639752)
-
(2006)
Investigative Ophthalmology and Visual Science
, vol.47
, Issue.7
, pp. 2820-2822
-
-
Aldave, A.J.1
Yellore, V.S.2
Salem, A.K.3
Yoo, G.L.4
Rayner, S.A.5
Yang, H.6
Tang, G.Y.7
Piconell, Y.8
Rabinowitz, Y.S.9
-
37
-
-
33748121986
-
SOD1: A candidate gene for keratoconus
-
DOI 10.1167/iovs.05-1500
-
Udar N, Atilano SR, Brown DJ, Holguin B, Small K, Nesburn AB, et al. SOD1: a candidate gene for keratoconus. Invest Ophthalmol Vis Sci 2006;47:3345-51. (Pubitemid 351639696)
-
(2006)
Investigative Ophthalmology and Visual Science
, vol.47
, Issue.8
, pp. 3345-3351
-
-
Udar, N.1
Atilano, S.R.2
Brown, D.J.3
Holguin, B.4
Small, K.5
Nesburn, A.B.6
Kenney, M.C.7
-
38
-
-
0026694804
-
Molecular genetic analysis in autosomal dominant keratoconus
-
Rabinowitz YS, Maumenee IH, Lundergan MK, Puffenberger E, Zhu D, Antonarakis S, et al. Molecular genetic analysis in autosomal dominant keratoconus. Cornea 1992;11:302-8.
-
(1992)
Cornea
, vol.11
, pp. 302-8
-
-
Rabinowitz, Y.S.1
Maumenee, I.H.2
Lundergan, M.K.3
Puffenberger, E.4
Zhu, D.5
Antonarakis, S.6
-
39
-
-
33745256448
-
The variable expression of keratoconus within monozygotic twins: Dundee University Scottish Keratoconus Study (DUSKS)
-
DOI 10.1016/j.clae.2006.03.003, PII S136704840600049X
-
Weed KH, MacEwen CJ, McGhee CN. The variable expression of keratoconus within monozygotic twins: Dundee University Scottish Keratoconus Study (DUSKS). Cont Lens Anterior Eye 2006;29:123-6. (Pubitemid 43923660)
-
(2006)
Contact Lens and Anterior Eye
, vol.29
, Issue.3
, pp. 123-126
-
-
Weed, K.H.1
MacEwen, C.J.2
McGhee, C.N.J.3
-
40
-
-
0033051834
-
Discordance for keratoconus in two pairs of monozygotic twins
-
McMahon TT, Shin JA, Newlin A, Edrington TB, Sugar J, Zadnik K. Discordance for keratoconus in two pairs of monozygotic twins. Cornea 1999;18:444-51. (Pubitemid 29294069)
-
(1999)
Cornea
, vol.18
, Issue.4
, pp. 444-451
-
-
McMahon, T.T.1
Shin, J.A.2
Newlin, A.3
Edrington, T.B.4
Sugar, J.5
Zadnik, K.6
-
41
-
-
0030042290
-
Keratoconus in two pairs of identical twins
-
Bechara SJ, Waring GO 3 rd, Insler MS. Keratoconus in two pairs of identical twins. Cornea 1996;15:90-3. (Pubitemid 26004915)
-
(1996)
Cornea
, vol.15
, Issue.1
, pp. 90-93
-
-
Bechara, S.J.1
Waring III, G.O.2
Insler, M.S.3
-
42
-
-
0024461696
-
Association between keratoconus and atopy
-
Harrison RJ, Klouda PT, Easty DL, Manku M, Charles J, Stewart CM. Association between keratoconus and atopy. Br J Ophthalmol 1989;73:816-22. (Pubitemid 19266407)
-
(1989)
British Journal of Ophthalmology
, vol.73
, Issue.10
, pp. 816-822
-
-
Harrison, R.J.1
Klouda, P.T.2
Easty, D.L.3
Manku, M.4
Charles, J.5
Stewart, J.C.C.M.6
-
43
-
-
0000840767
-
Mongolism (Downs syndrome) and keratoconus
-
Cullen JF, Butler HG. Mongolism (Downs syndrome) and keratoconus. Br J Ophthalmol 1963;47:321-30.
-
(1963)
Br J Ophthalmol
, vol.47
, pp. 321-30
-
-
Cullen, J.F.1
Butler, H.G.2
-
44
-
-
0028331862
-
Leber congenital amaurosis and its association with keratoconus and keratoglobus
-
Elder MJ. Leber congenital amaurosis and its association with keratoconus and keratoglobus. J Pediatr Ophthalmol Strabismus 1994;31:38-40. (Pubitemid 24109498)
-
(1994)
Journal of Pediatric Ophthalmology and Strabismus
, vol.31
, Issue.1
, pp. 38-40
-
-
Elder, M.J.1
-
45
-
-
0029286338
-
Autosomal dominant keratoconusas the chief ocular symptom in Lobstein osteogenesisimperfecta tarda (in German)
-
Beckh U, Schonherr U, Naumann GO. Autosomal dominant keratoconusas the chief ocular symptom in Lobstein osteogenesisimperfecta tarda (in German). Klinische Monatsblatter fur Augenheilkunde 1995;206:268-72.
-
(1995)
Klinische Monatsblatter fur Augenheilkunde
, vol.206
, pp. 268-72
-
-
Beckh, U.1
Schonherr, U.2
Naumann, G.O.3
-
46
-
-
0025011537
-
GAPO syndrome (McKusick 23074): A connective tissue disorder-report on two affected sibs and on the pathologic findings in the older
-
Wajntal A, Koiffmann CP, Mendonça BB, Epps-Quaglia D, Sotto MN, Rati PB, et al. GAPO syndrome (McKusick 23074): a connective tissue disorder-report on two affected sibs and on the pathologic findings in the older. Am J Med Genet 1990;37:213-23.
-
(1990)
Am J Med Genet
, vol.37
, pp. 213-23
-
-
Wajntal, A.K.1
-
47
-
-
0017663296
-
Ehlers-Danlos syndrome associated with keratoconus: A case report
-
Kuming BS, Joffe L. Ehlers-Danlos syndrome associated with keratoconus: a case report. S Afr Med J 1977;52:403-5. (Pubitemid 8176095)
-
(1977)
South African Medical Journal
, vol.52
, Issue.10
, pp. 403-405
-
-
Kuming, B.S.1
Joffe, L.2
-
48
-
-
0016788205
-
Keratoconus and the Ehlers-Danlos syndrome: A new aspect of keratoconus
-
Robertson I. Keratoconus and the Ehlers-Danlos syndrome: a new aspect of keratoconus. Med J Aust 1975;1:571-3.
-
(1975)
Med J Aust
, vol.1
, pp. 571-3
-
-
Robertson, I.1
-
49
-
-
0021792234
-
The ocular features of Downs syndrome
-
Shapiro MB, France TD. The ocular features of Downs syndrome. Am J Ophthalmol 1985;99:659-63.
-
(1985)
Am J Ophthalmol
, vol.99
, pp. 659-63
-
-
Shapiro, M.B.1
France, T.D.2
-
51
-
-
3442899349
-
Prevalence of ocular diagnoses found on screening 1539 adults with intellectual disabilities
-
DOI 10.1016/j.ophtha.2003.12.051, PII S0161642004003331
-
van Splunder J, Stilma JS, Bernsen RM, Evenhuis HM. Prevalence of ocular diagnoses found on screening 1539 adults with intellectual disabilities. 1: Ophthalmology 2004;111:1457-63. (Pubitemid 39030795)
-
(2004)
Ophthalmology
, vol.111
, Issue.8
, pp. 1457-1463
-
-
Van Splunder, J.1
Stilma, J.S.2
Bernsen, R.M.D.3
Evenhuis, H.M.4
-
52
-
-
67649989556
-
CRB1 gene mutations are associated with keratoconus in patients with Leber congenital amaurosis
-
McMahon TT, Kim LS, Fishman GA, Stone EM, Zhao XC, Yee RW, et al. CRB1 gene mutations are associated with keratoconus in patients with Leber congenital amaurosis. Invest Ophthalmol Vis Sci 2009;50:3185-7.
-
(2009)
Invest Ophthalmol Vis Sci
, vol.50
, pp. 3185-7
-
-
McMahon, T.T.1
Kim, L.S.2
Fishman, G.A.3
Stone, E.M.4
Zhao, X.C.5
Yee, R.W.6
-
54
-
-
0034037349
-
Keratoconus and mitral valve prolapse
-
DOI 10.1016/S0002-9394(00)00371-8, PII S0002939400003718
-
Lichter H, Loya N, Sagie A, Cohen N, Muzmacher L, Yassur Y, Weinberger D. Keratoconus and mitral valve prolapse. Am J Ophthalmol 2000;129:667-8. (Pubitemid 30323737)
-
(2000)
American Journal of Ophthalmology
, vol.129
, Issue.5
, pp. 667-668
-
-
Lichter, H.1
Loya, N.2
Sagie, A.3
Cohen, N.4
Muzmacher, L.5
Yassur, Y.6
Weinberger, D.7
-
55
-
-
0026548380
-
Keratoconus in the mentally retarded
-
Haugen OH. Keratoconus in the mentally retarded. Acta Ophthalmol (Copenh) 1992;70:111-4.
-
(1992)
Acta Ophthalmol (Copenh)
, vol.70
, pp. 111-4
-
-
Haugen, O.H.1
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