-
1
-
-
0242412062
-
Doyne's discoid cataract
-
Adams P.H. Doyne's discoid cataract. Br J Ophthalmol. 26:1942;152-153.
-
(1942)
Br J Ophthalmol
, vol.26
, pp. 152-153
-
-
Adams, P.H.1
-
2
-
-
0028835546
-
A progressive early onset cataract gene maps to human chromosome 17q24
-
Armitage M.M., Kivlin J.D., Ferrell R.E. A progressive early onset cataract gene maps to human chromosome 17q24. Nat Genet. 9:1995;37-40.
-
(1995)
Nat Genet
, vol.9
, pp. 37-40
-
-
Armitage, M.M.1
Kivlin, J.D.2
Ferrell, R.E.3
-
4
-
-
0017345397
-
Sector shaped membranous cataract
-
Bartholomew R.S. Sector shaped membranous cataract. J Pediatr Ophthalmol. 14:1977;109-111.
-
(1977)
J Pediatr Ophthalmol
, vol.14
, pp. 109-111
-
-
Bartholomew, R.S.1
-
5
-
-
0030043232
-
Autosomal dominant zonular cataract with sutural opacities in a four-generation family
-
Basti S., Hejtmancik J.F., Padma T.et al. Autosomal dominant zonular cataract with sutural opacities in a four-generation family. Am J Ophthalmol. 121:1996;162-168.
-
(1996)
Am J Ophthalmol
, vol.121
, pp. 162-168
-
-
Basti, S.1
Hejtmancik, J.F.2
Padma, T.3
-
6
-
-
0033623351
-
A new betaA1-crystallin splice junction mutation in autosomal dominant cataract
-
Bateman J.B., Geyer D.D., Flodman P.et al. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract. Invest Ophthalmol Vis Sci. 41:2000;3278-3285.
-
(2000)
Invest Ophthalmol Vis Sci
, vol.41
, pp. 3278-3285
-
-
Bateman, J.B.1
Geyer, D.D.2
Flodman, P.3
-
8
-
-
0027516942
-
Ophthalmic findings in classical galactosaemia - Prospective study
-
Beigi B., OKeefe M., Bowell R.et al. Ophthalmic findings in classical galactosaemia - prospective study. Br J Ophthalmol. 77:1993;162-164.
-
(1993)
Br J Ophthalmol
, vol.77
, pp. 162-164
-
-
Beigi, B.1
OKeefe, M.2
Bowell, R.3
-
9
-
-
0020051079
-
The natural history of congenital sutural cataracts. Case report with long-term follow-up
-
Bercovitch L., Donaldson D.D. The natural history of congenital sutural cataracts. Case report with long-term follow-up. J Pediatr Ophthalmol Strabismus. 19:1982;108-110.
-
(1982)
J Pediatr Ophthalmol Strabismus
, vol.19
, pp. 108-110
-
-
Bercovitch, L.1
Donaldson, D.D.2
-
10
-
-
0029935270
-
Ocular findings in 55 patients with Downs syndrome
-
Berk A.T., Saatci A.O., Ercal M.D.et al. Ocular findings in 55 patients with Downs syndrome. Ophthalmic Genet. 17:1996;15-19.
-
(1996)
Ophthalmic Genet
, vol.17
, pp. 15-19
-
-
Berk, A.T.1
Saatci, A.O.2
Ercal, M.D.3
-
11
-
-
0034765821
-
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans
-
Berry V., Francis P., Reddy M.A.et al. Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans. Am J Hum Genet. 69:2001;1141-1145.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1141-1145
-
-
Berry, V.1
Francis, P.2
Reddy, M.A.3
-
12
-
-
0030066487
-
A locus for autosomal dominant anterior polar cataract on chromosome 17p
-
Berry V., Ionides A.C., Moore A.T.et al. A locus for autosomal dominant anterior polar cataract on chromosome 17p. Hum Mol Genet. 5:1996;415-419.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 415-419
-
-
Berry, V.1
Ionides, A.C.2
Moore, A.T.3
-
13
-
-
0021241836
-
The Nance-Horan syndrome: A rare X-linked ocular-dental trait with expression in heterozygous females
-
Bixler D., Higgins M., Hartsfield J. Jr. The Nance-Horan syndrome. a rare X-linked ocular-dental trait with expression in heterozygous females Clin Genet. 26:1984;30-35.
-
(1984)
Clin Genet
, vol.26
, pp. 30-35
-
-
Bixler, D.1
Higgins, M.2
Hartsfield J., Jr.3
-
14
-
-
85046197380
-
Congenital membranous cataract
-
Blake E.M. Congenital membranous cataract. Am J Ophthalmol. 29:1946;464.
-
(1946)
Am J Ophthalmol
, vol.29
, pp. 464
-
-
Blake, E.M.1
-
16
-
-
0019515032
-
Spontaneous absorption of the lens in the congenital rubella syndrome
-
Boger W.P. 3rd, Petersen R.A., Robb R.M. Spontaneous absorption of the lens in the congenital rubella syndrome. Arch Ophthalmol. 99:1981;433-434.
-
(1981)
Arch Ophthalmol
, vol.99
, pp. 433-434
-
-
Boger W.P. III1
Petersen, R.A.2
Robb, R.M.3
-
18
-
-
0026671929
-
Anterior polar congenital cataract and corneal astigmatism
-
Bouzas A.G. Anterior polar congenital cataract and corneal astigmatism. J Pediatr Ophthalmol Strabismus. 29:2000;210-212.
-
(2000)
J Pediatr Ophthalmol Strabismus
, vol.29
, pp. 210-212
-
-
Bouzas, A.G.1
-
19
-
-
0026671929
-
Anterior polar congenital cataract and corneal astigmatism
-
Bouzas A.G. Anterior polar congenital cataract and corneal astigmatism. J Pediatr Ophthalmol Strabismus. 29:1992;210-212.
-
(1992)
J Pediatr Ophthalmol Strabismus
, vol.29
, pp. 210-212
-
-
Bouzas, A.G.1
-
21
-
-
0018346470
-
Anterior polar cataracts associated with bilateral retinoblastoma
-
Brown G.C., Shields J.A., Oglesby R.B. Anterior polar cataracts associated with bilateral retinoblastoma. Am J Ophthalmol. 87:1979;276.
-
(1979)
Am J Ophthalmol
, vol.87
, pp. 276
-
-
Brown, G.C.1
Shields, J.A.2
Oglesby, R.B.3
-
22
-
-
0004250428
-
-
Oxford: Butterworth-Heinemann Ltd
-
Brown N., Bron A.J. Lens disorders. 1996;133-193 Butterworth-Heinemann Ltd, Oxford.
-
(1996)
Lens Disorders
, pp. 133-193
-
-
Brown, N.1
Bron, A.J.2
-
23
-
-
0015255433
-
Anterior polar pyramidal cataract. Presenting as an anterior chamber foreign body
-
Brown N., Ellis P. Anterior polar pyramidal cataract. Presenting as an anterior chamber foreign body. Br J Ophthalmol. 56:1972;57-59.
-
(1972)
Br J Ophthalmol
, vol.56
, pp. 57-59
-
-
Brown, N.1
Ellis, P.2
-
24
-
-
0017082297
-
Lowe syndrome: Identification of the carrier state
-
Brown N., Gardner R.J. Lowe syndrome. identification of the carrier state Birth Defects Orig Artic Ser. 12:1976;579-595.
-
(1976)
Birth Defects Orig Artic Ser
, vol.12
, pp. 579-595
-
-
Brown, N.1
Gardner, R.J.2
-
25
-
-
0023676121
-
Central compaction in the process of lens growth as indicated by lamellar cataract
-
Brown N.A., Sparrow J.M., Bron A.J. Central compaction in the process of lens growth as indicated by lamellar cataract. Br J Ophthalmol. 72:1988;538-544.
-
(1988)
Br J Ophthalmol
, vol.72
, pp. 538-544
-
-
Brown, N.A.1
Sparrow, J.M.2
Bron, A.J.3
-
26
-
-
0242412060
-
Galactosemia in an infant with cataracts: Clinical observations and carbohydrate studies
-
Bruck E., Rapoport S. Galactosemia in an infant with cataracts. clinical observations and carbohydrate studies Am J Dis Child. 70:1945;267.
-
(1945)
Am J Dis Child
, vol.70
, pp. 267
-
-
Bruck, E.1
Rapoport, S.2
-
28
-
-
0000093155
-
Lenticonus posterior: Report of six cases
-
Butler T.H. Lenticonus posterior. report of six cases Arch Ophthalmol. 3:1930;425-436.
-
(1930)
Arch Ophthalmol
, vol.3
, pp. 425-436
-
-
Butler, T.H.1
-
31
-
-
0020466792
-
A syndrome involving congenital cataracts of unusual morphology, microcornea, abnormal irides, nystagmus and congenital glaucoma, inherited as an autosomal dominant trait
-
Cebon L., West R.H. A syndrome involving congenital cataracts of unusual morphology, microcornea, abnormal irides, nystagmus and congenital glaucoma, inherited as an autosomal dominant trait. Aust J Ophthalmol. 10:1982;237-242.
-
(1982)
Aust J Ophthalmol
, vol.10
, pp. 237-242
-
-
Cebon, L.1
West, R.H.2
-
32
-
-
0034755009
-
Lens changes in hereditary hyperferritinemia-cataract syndrome
-
Chang-Godinich A., Ades S., Schenkein D.et al. Lens changes in hereditary hyperferritinemia-cataract syndrome. Am J Ophthalmol. 132:2001;786-788.
-
(2001)
Am J Ophthalmol
, vol.132
, pp. 786-788
-
-
Chang-Godinich, A.1
Ades, S.2
Schenkein, D.3
-
34
-
-
0035112430
-
Pyramidal anterior polar cataracts
-
Christensen G.R. Pyramidal anterior polar cataracts. Ophthalmology. 108:2001;430-431.
-
(2001)
Ophthalmology
, vol.108
, pp. 430-431
-
-
Christensen, G.R.1
-
36
-
-
0014359440
-
Recent example of variability of types of congenital cataract in the same family
-
Collier M: [Recent example of variability of types of congenital cataract in the same family]. Bull Soc Ophtalmol Fr 68:910-1, 1968.
-
(1968)
Bull Soc Ophtalmol Fr
, vol.68
, pp. 910-911
-
-
Collier, M.1
-
37
-
-
0242495397
-
Developmental deformities of the crystalline lens
-
Collins ET: Developmental deformities of the crystalline lens. Ophthalmoscope 6:577-83, 663, 1908.
-
(1908)
Ophthalmoscope
, vol.6
, pp. 577-583
-
-
Collins, E.T.1
-
38
-
-
0242579757
-
Galactosemia cataract: A review
-
Cordes F.C. Galactosemia cataract. a review Am J Ophthalmol. 50:1960;1151-1158.
-
(1960)
Am J Ophthalmol
, vol.50
, pp. 1151-1158
-
-
Cordes, F.C.1
-
39
-
-
0242579758
-
Evaluation of the surgery of congenital cataracts
-
Cordes F.C. Evaluation of the surgery of congenital cataracts. Arch Ophthalmol. 46:1951;132-144.
-
(1951)
Arch Ophthalmol
, vol.46
, pp. 132-144
-
-
Cordes, F.C.1
-
40
-
-
0001699788
-
Conservatism in the management of congenital cataracts
-
Costenbader F.D., Albert D.G. Conservatism in the management of congenital cataracts. Arch Ophthalmol. 58:1957;426-430.
-
(1957)
Arch Ophthalmol
, vol.58
, pp. 426-430
-
-
Costenbader, F.D.1
Albert, D.G.2
-
41
-
-
0017691618
-
Conservative management of cataracts
-
Crawford J.S. Conservative management of cataracts. Int Ophthalmol Clin. 17:1977;31-35.
-
(1977)
Int Ophthalmol Clin
, vol.17
, pp. 31-35
-
-
Crawford, J.S.1
-
42
-
-
0017872839
-
Management of posterior lenticonus complicated by unilateral cataract
-
Crouch E.R. Jr., Parks M.M. Management of posterior lenticonus complicated by unilateral cataract. Am J Ophthalmol. 85:1978;503-508.
-
(1978)
Am J Ophthalmol
, vol.85
, pp. 503-508
-
-
Crouch E.R., Jr.1
Parks, M.M.2
-
43
-
-
0023025901
-
Features of a syndrome with congenital cataract and hypertrophic car-diomyopathy
-
Cruysberg J.R., Sengers R.C., Pinckers A.et al. Features of a syndrome with congenital cataract and hypertrophic car-diomyopathy. Am J Ophthalmol. 102:1986;740-749.
-
(1986)
Am J Ophthalmol
, vol.102
, pp. 740-749
-
-
Cruysberg, J.R.1
Sengers, R.C.2
Pinckers, A.3
-
44
-
-
0029783030
-
Ocular findings in Downs syndrome
-
da Cunha R.P., Moreira J.B. Ocular findings in Downs syndrome. Am J Ophthalmol. 122:1996;236-244.
-
(1996)
Am J Ophthalmol
, vol.122
, pp. 236-244
-
-
Da Cunha, R.P.1
Moreira, J.B.2
-
45
-
-
0033498332
-
Surgical results of persistent hyperplastic primary vitreous
-
Dass A.B., Trese M.T. Surgical results of persistent hyperplastic primary vitreous. Ophthalmology. 106:1999;280-284.
-
(1999)
Ophthalmology
, vol.106
, pp. 280-284
-
-
Dass, A.B.1
Trese, M.T.2
-
46
-
-
0027399921
-
Congenital zonular cataract. Clinicopathologic correlation with electron microscopy and review of the literature
-
de Gottrau P., Schlotzer-Schrehardt U., Dorfler S., Naumann G.O. Congenital zonular cataract. Clinicopathologic correlation with electron microscopy and review of the literature. Arch Ophthalmol. 111:1993;235-239.
-
(1993)
Arch Ophthalmol
, vol.111
, pp. 235-239
-
-
De Gottrau, P.1
Schlotzer-Schrehardt, U.2
Dorfler, S.3
Naumann, G.O.4
-
47
-
-
0025102681
-
Crystalline cataract and uncombable hair. Ultrastructural and biochemical findings
-
de Jong P.T., Bleeker-Wagemakers E.M., Vrensen G.F.et al. Crystalline cataract and uncombable hair. Ultrastructural and biochemical findings. Ophthalmology. 97:1990;1181-1187.
-
(1990)
Ophthalmology
, vol.97
, pp. 1181-1187
-
-
De Jong, P.T.1
Bleeker-Wagemakers, E.M.2
Vrensen, G.F.3
-
48
-
-
0025848108
-
Anterior lentiplane and posterior lenticonus in two cases
-
Deng C. Anterior lentiplane and posterior lenticonus in two cases. Ophthalmologica. 202:1991;187-190.
-
(1991)
Ophthalmologica
, vol.202
, pp. 187-190
-
-
Deng, C.1
-
52
-
-
84979145227
-
Familial cornea guttata in association with anterior polar cataracts
-
Dohlman C.H. Familial cornea guttata in association with anterior polar cataracts. Acta Ophthalmol. 29:1951;445-451.
-
(1951)
Acta Ophthalmol
, vol.29
, pp. 445-451
-
-
Dohlman, C.H.1
-
55
-
-
0033786113
-
Overexpression of PAX6(5a) in lens fiber cells results in cataract and upregulation of (alpha)5(beta)1 integrin expression
-
Duncan M.K., Kozmik Z., Cveklova K.et al. Overexpression of PAX6(5a) in lens fiber cells results in cataract and upregulation of (alpha)5(beta)1 integrin expression. J Cell Sci. 113:2000;3173-3185.
-
(2000)
J Cell Sci
, vol.113
, pp. 3173-3185
-
-
Duncan, M.K.1
Kozmik, Z.2
Cveklova, K.3
-
57
-
-
0242663768
-
Spontanous absorption of congenital cataract following maternal rubella
-
Ehrlich L.H. Spontanous absorption of congenital cataract following maternal rubella. Arch Ophthalmol. 39:1948;205-209.
-
(1948)
Arch Ophthalmol
, vol.39
, pp. 205-209
-
-
Ehrlich, L.H.1
-
58
-
-
0029002373
-
Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36
-
Eiberg H., Lund A.M., Warburg M., Rosenberg T. Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36. Hum Genet. 96:1995;33-38.
-
(1995)
Hum Genet
, vol.96
, pp. 33-38
-
-
Eiberg, H.1
Lund, A.M.2
Warburg, M.3
Rosenberg, T.4
-
59
-
-
0242495395
-
Lenticonus posterior
-
Elschnig Lenticonus posterior. Klin Monatsbl Augenheilkd. 33:1895;239-243.
-
(1895)
Klin Monatsbl Augenheilkd
, vol.33
, pp. 239-243
-
-
Elschnig1
-
60
-
-
0020279434
-
Human posterior subcapsular cataracts
-
Eshagian J. Human posterior subcapsular cataracts. Trans Ophthalmol Soc UK. 102:1982;364-368.
-
(1982)
Trans Ophthalmol Soc UK
, vol.102
, pp. 364-368
-
-
Eshagian, J.1
-
61
-
-
0026011898
-
Lowes oculocerebrorenal syndrome - Variation in lens changes in the carrier state
-
Fagerholm P., Anneren G., Wadelius C. Lowes oculocerebrorenal syndrome - variation in lens changes in the carrier state. Acta Ophthalmol (Copenh). 69:1991;102-104.
-
(1991)
Acta Ophthalmol (Copenh)
, vol.69
, pp. 102-104
-
-
Fagerholm, P.1
Anneren, G.2
Wadelius, C.3
-
63
-
-
0001564139
-
Hallermann-Streiff syndrome: A dyscephaly with congenital cataracts and hypotrichosis
-
Falls H.F., Schull W.J. Hallermann-Streiff syndrome. a dyscephaly with congenital cataracts and hypotrichosis Arch Ophthalmol. 63:1960;419-420.
-
(1960)
Arch Ophthalmol
, vol.63
, pp. 419-420
-
-
Falls, H.F.1
Schull, W.J.2
-
64
-
-
0242663767
-
The late acquisition of vision by persons born blind as the result of bilateral congenital cataracts
-
Fisher Miller C. The late acquisition of vision by persons born blind as the result of bilateral congenital cataracts. Trans Am Neurol Assn. 89:1964;195-197.
-
(1964)
Trans Am Neurol Assn
, vol.89
, pp. 195-197
-
-
Fisher Miller, C.1
-
66
-
-
0021986965
-
Anterior subcapsular cataracts: A review of potential etiologies
-
Flach A.J., Peterson J.S., Dolan B.J. Anterior subcapsular cataracts. a review of potential etiologies Ann Ophthalmol. 17:1995;78-80.
-
(1995)
Ann Ophthalmol
, vol.17
, pp. 78-80
-
-
Flach, A.J.1
Peterson, J.S.2
Dolan, B.J.3
-
68
-
-
0033675222
-
Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens
-
Francis P., Berry V., Bhattacharya S., Moore A. Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens. Br J Ophthalmol. 84:2000;1376-1379.
-
(2000)
Br J Ophthalmol
, vol.84
, pp. 1376-1379
-
-
Francis, P.1
Berry, V.2
Bhattacharya, S.3
Moore, A.4
-
70
-
-
0034981273
-
Visual outcome in patients with isolated autosomal dominant congenital cataract
-
Francis P.J., Ionides A., Berry V.et al. Visual outcome in patients with isolated autosomal dominant congenital cataract. Ophthalmology. 108:2001;1104-1108.
-
(2001)
Ophthalmology
, vol.108
, pp. 1104-1108
-
-
Francis, P.J.1
Ionides, A.2
Berry, V.3
-
71
-
-
0028037015
-
Cloudy lenses and issues: A pedigree of unoperated congenital cataracts
-
Freeman R.S., Rovick L.P. Cloudy lenses and issues. a pedigree of unoperated congenital cataracts J Pediatr Ophthalmol Strabismus. 31:1994;318-322.
-
(1994)
J Pediatr Ophthalmol Strabismus
, vol.31
, pp. 318-322
-
-
Freeman, R.S.1
Rovick, L.P.2
-
72
-
-
0014858339
-
Concurrence of hereditary congenital cataracts and hereditary retinoblastoma
-
Friendly D.S., Parks M.M. Concurrence of hereditary congenital cataracts and hereditary retinoblastoma. Arch Ophthalmol. 84:1970;525-527.
-
(1970)
Arch Ophthalmol
, vol.84
, pp. 525-527
-
-
Friendly, D.S.1
Parks, M.M.2
-
73
-
-
0035078480
-
The assessment of lens opacities in clinical practice: Results of a national survey
-
Frost N.A., Sparrow J.M. The assessment of lens opacities in clinical practice. results of a national survey Br J Ophthalmol. 85:2001;319-321.
-
(2001)
Br J Ophthalmol
, vol.85
, pp. 319-321
-
-
Frost, N.A.1
Sparrow, J.M.2
-
74
-
-
0015469128
-
Cataract in the shape of lifesaver
-
Gailloud C, Streiff EB: [Cataract in the shape of lifesaver]. Ophthalmologica 165:212-8, 1972.
-
(1972)
Ophthalmologica
, vol.165
, pp. 212-218
-
-
Gailloud, C.1
Streiff, E.B.2
-
75
-
-
0017146139
-
The Stickler syndrome (hereditary arthro-ophthalmopathy)
-
Gellis S.S. The Stickler syndrome (hereditary arthro-ophthalmopathy). Am J Dis Child. 130:1976;65-66.
-
(1976)
Am J Dis Child
, vol.130
, pp. 65-66
-
-
Gellis, S.S.1
-
78
-
-
84895292029
-
Hereditary galactokinase deficiency, a newly recognised cause of juvenile cataracts
-
Gitzelmann R. Hereditary galactokinase deficiency, a newly recognised cause of juvenile cataracts. Pediatr Res. 1:1967;14-23.
-
(1967)
Pediatr Res
, vol.1
, pp. 14-23
-
-
Gitzelmann, R.1
-
79
-
-
0030785316
-
Persistent fetal vasculature (PFV): An integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture
-
Goldberg M.F. Persistent fetal vasculature (PFV). an integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture Am J Ophthalmol. 124:1997;587-626.
-
(1997)
Am J Ophthalmol
, vol.124
, pp. 587-626
-
-
Goldberg, M.F.1
-
80
-
-
0021795785
-
Refractive development of the human eye
-
Gordon R.A., Donzis P.B. Refractive development of the human eye. Arch Ophthalmol. 103:1985;785-789.
-
(1985)
Arch Ophthalmol
, vol.103
, pp. 785-789
-
-
Gordon, R.A.1
Donzis, P.B.2
-
81
-
-
0020626685
-
Ocular manifestations of Alports syndrome: A hereditary disorder of basement membranes?
-
Govan J.A. Ocular manifestations of Alports syndrome. a hereditary disorder of basement membranes? Br J Ophthalmol. 67:1983;493-503.
-
(1983)
Br J Ophthalmol
, vol.67
, pp. 493-503
-
-
Govan, J.A.1
-
82
-
-
0012777496
-
Galactose studies in an infant with idiopathic galactose intolerance
-
Greenman L., Rathbun J.C. Galactose studies in an infant with idiopathic galactose intolerance. Pediatrics. 2:1948;666.
-
(1948)
Pediatrics
, vol.2
, pp. 666
-
-
Greenman, L.1
Rathbun, J.C.2
-
83
-
-
0242579754
-
Notes on some forms of congenital cataract
-
Gunn D. Notes on some forms of congenital cataract. Ophthalmic Rev. 17:1998;129-143.
-
(1998)
Ophthalmic Rev
, vol.17
, pp. 129-143
-
-
Gunn, D.1
-
84
-
-
0242663766
-
Peculiar coralliform cataract with crystals of cholesterine in the lens
-
Gunn R.M. Peculiar coralliform cataract with crystals of cholesterine in the lens. Trans Ophthalmol Soc UK. 15:1895;119.
-
(1895)
Trans Ophthalmol Soc UK
, vol.15
, pp. 119
-
-
Gunn, R.M.1
-
85
-
-
0015391333
-
Coralliform cataracts
-
Guyot-Sionnest: [Coralliform cataracts]. Bull Soc Ophtalmol Fr 72:881-7, 1972.
-
(1972)
Bull Soc Ophtalmol Fr
, vol.72
, pp. 881-887
-
-
-
86
-
-
0018165133
-
Persistent hyperplastic primary vitreous. A clinicopathologic study of. 62 cases and review of the literature
-
Haddad R., Font R.L., Reeser F. Persistent hyperplastic primary vitreous. A clinicopathologic study of. 62(cases and review of the literature. Surv Ophthalmol 23):1978;123-134.
-
(1978)
Surv Ophthalmol
, vol.23
, pp. 123-134
-
-
Haddad, R.1
Font, R.L.2
Reeser, F.3
-
87
-
-
0021105205
-
Sectorial cataract: A possible example of lyonisation
-
Happle R., Kuchle H.J. Sectorial cataract. a possible example of lyonisation Lancet. 2:1983;919-920.
-
(1983)
Lancet
, vol.2
, pp. 919-920
-
-
Happle, R.1
Kuchle, H.J.2
-
88
-
-
0242495394
-
Ten pedigrees of congenital and infantile cataract
-
Harman N.B. Ten pedigrees of congenital and infantile cataract. Trans Ophthalmol Soc UK. 30:1910;251-274.
-
(1910)
Trans Ophthalmol Soc UK
, vol.30
, pp. 251-274
-
-
Harman, N.B.1
-
90
-
-
0023126217
-
Cerebro-ocular dysplasia - Muscular dystrophy syndrome. Report of two cases
-
Heggie P., Grossniklaus H.E., Roessmann U.et al. Cerebro-ocular dysplasia - muscular dystrophy syndrome. Report of two cases. Arch Ophthalmol. 105:1987;520-524.
-
(1987)
Arch Ophthalmol
, vol.105
, pp. 520-524
-
-
Heggie, P.1
Grossniklaus, H.E.2
Roessmann, U.3
-
91
-
-
0035094223
-
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22
-
Heon E., Paterson A.D., Fraser M.et al. A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22. Am J Hum Genet. 68:2001;772-777.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 772-777
-
-
Heon, E.1
Paterson, A.D.2
Fraser, M.3
-
92
-
-
85031200572
-
-
Leipzig: Verlag von Engelmann
-
Hess C. Die angeborenen Starformen, in Graefe Saemisch Handbuch der gesamten Augenheilkunde, 3.Auflage, Part 2, Kap. 9. 1911;178-225 Verlag von Engelmann, Leipzig.
-
(1911)
Die Angeborenen Starformen, in Graefe Saemisch Handbuch der gesamten Augenheilkunde, 3.Auflage, Part 2, Kap. 9
, pp. 178-225
-
-
Hess, C.1
-
93
-
-
0021721377
-
Intraocular lens implantation in children with monocular cataracts. 1974-1983
-
Hiles D.A. Intraocular lens implantation in children with monocular cataracts. 1974-1983. Ophthalmology. 91:1984;1231-1237.
-
(1984)
Ophthalmology
, vol.91
, pp. 1231-1237
-
-
Hiles, D.A.1
-
94
-
-
0017708819
-
Classification of cataracts in children
-
Hiles D.A., Carter B.T. Classification of cataracts in children. Int Ophthalmol Clin. 17:1977;15-29.
-
(1977)
Int Ophthalmol Clin
, vol.17
, pp. 15-29
-
-
Hiles, D.A.1
Carter, B.T.2
-
97
-
-
0017855141
-
Linkage relations of a locus for congenital total nuclear cataract
-
Huntzinger R.S., Weitkamp L.R., Roca P.D. Linkage relations of a locus for congenital total nuclear cataract. J Med Genet. 15:1978;113-115.
-
(1978)
J Med Genet
, vol.15
, pp. 113-115
-
-
Huntzinger, R.S.1
Weitkamp, L.R.2
Roca, P.D.3
-
98
-
-
0003390853
-
The relationship of lenticular changes in Mongolism
-
Ingersheim J. The relationship of lenticular changes in Mongolism. Trans Am Ophthalmol Soc. 49:1951;595-624.
-
(1951)
Trans Am Ophthalmol Soc
, vol.49
, pp. 595-624
-
-
Ingersheim, J.1
-
99
-
-
0032792185
-
Clinical and genetic heterogeneity in autosomal dominant cataract
-
Ionides A., Francis P., Berry V.et al. Clinical and genetic heterogeneity in autosomal dominant cataract. Br J Ophthalmol. 83:1999;802-808.
-
(1999)
Br J Ophthalmol
, vol.83
, pp. 802-808
-
-
Ionides, A.1
Francis, P.2
Berry, V.3
-
100
-
-
0031021393
-
A locus for autosomal dominant posterior polar cataract on chromosome 1p
-
Ionides A.C., Berry V., Mackay D.S.et al. A locus for autosomal dominant posterior polar cataract on chromosome 1p. Hum Mol Genet. 6:1997;47-51.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 47-51
-
-
Ionides, A.C.1
Berry, V.2
Mackay, D.S.3
-
101
-
-
0028564825
-
Sutural cataract, retinitis pigmentosa, microcephaly and psychomotor retardation. A new autosomal recessive disorder?
-
Ippel P.F., Wittebol-Post D., van Nesselrooij B.P., Bijlsma J.B. Sutural cataract, retinitis pigmentosa, microcephaly and psychomotor retardation. A new autosomal recessive disorder? Ophthalmic Genet. 15:1994;121-127.
-
(1994)
Ophthalmic Genet
, vol.15
, pp. 121-127
-
-
Ippel, P.F.1
Wittebol-Post, D.2
Van Nesselrooij, B.P.3
Bijlsma, J.B.4
-
102
-
-
0021342011
-
Congenital anterior polar cataract: A review of 63 cases
-
Jaafar M.S., Robb R.M. Congenital anterior polar cataract. a review of 63 cases Ophthalmology. 91:1984;249-254.
-
(1984)
Ophthalmology
, vol.91
, pp. 249-254
-
-
Jaafar, M.S.1
Robb, R.M.2
-
103
-
-
0026635156
-
Ophthalmologic assessment of young patients with Alport syndrome
-
Jacobs M., Jeffrey B., Kriss A.et al. Ophthalmologic assessment of young patients with Alport syndrome. Ophthalmology. 99:1992;1039-1044.
-
(1992)
Ophthalmology
, vol.99
, pp. 1039-1044
-
-
Jacobs, M.1
Jeffrey, B.2
Kriss, A.3
-
104
-
-
0019231777
-
Ocular findings in Downs syndrome
-
Jaeger E.A. Ocular findings in Downs syndrome. Trans Am Ophthalmol Soc. 78:1980;808-845.
-
(1980)
Trans Am Ophthalmol Soc
, vol.78
, pp. 808-845
-
-
Jaeger, E.A.1
-
106
-
-
0242579753
-
Lenticonus Posterior Zeitschrift
-
Jano A. Lenticonus Posterior Zeitschrift. Augenheilkd. 38:1917;192-197.
-
(1917)
Augenheilkd
, vol.38
, pp. 192-197
-
-
Jano, A.1
-
107
-
-
0017086904
-
Ocular manifestations in patients and female relatives of families with the oculocerebrorenal syndrome of Lowe
-
Johnson S.S., Nevin N.C. Ocular manifestations in patients and female relatives of families with the oculocerebrorenal syndrome of Lowe. Birth Defects. 12:1976;567-572.
-
(1976)
Birth Defects
, vol.12
, pp. 567-572
-
-
Johnson, S.S.1
Nevin, N.C.2
-
108
-
-
0022546028
-
Visual acuity results following treatment of persistent hyperplastic primary vitreous
-
Karr D.J., Scott W.E. Visual acuity results following treatment of persistent hyperplastic primary vitreous. Arch Ophthalmol. 104:1986;662-667.
-
(1986)
Arch Ophthalmol
, vol.104
, pp. 662-667
-
-
Karr, D.J.1
Scott, W.E.2
-
109
-
-
0021713472
-
Posterior lenticonus
-
Khalil M., Saheb N. Posterior lenticonus. Ophthalmology. 91:1984;1429-1430., 43A,
-
(1984)
Ophthalmology
, vol.91
, pp. 1429-1430
-
-
Khalil, M.1
Saheb, N.2
-
110
-
-
0027245757
-
Unilateral posterior lenticonus with persistent hyaloid artery remnant
-
Kilty L.A., Hiles D.A. Unilateral posterior lenticonus with persistent hyaloid artery remnant. Am J Ophthalmol. 116:1993;104-106.
-
(1993)
Am J Ophthalmol
, vol.116
, pp. 104-106
-
-
Kilty, L.A.1
Hiles, D.A.2
-
111
-
-
0242412056
-
Cataracte familiale d'un type particulier apparament suivant le mode dominant
-
Koby F.E. Cataracte familiale d'un type particulier apparament suivant le mode dominant. Arch Ophthalmol. 38:1923;492-501.
-
(1923)
Arch Ophthalmol
, vol.38
, pp. 492-501
-
-
Koby, F.E.1
-
112
-
-
0021731784
-
Significance of early ophthalmologic detection of Fabry disease
-
Konrad G, Kohlschutter A, Aust W: [Significance of early ophthalmologic detection of Fabry disease]. Klin Monatsbl Augenheilkd 185:535-8, 1984.
-
(1984)
Klin Monatsbl Augenheilkd
, vol.185
, pp. 535-538
-
-
Konrad, G.1
Kohlschutter, A.2
Aust, W.3
-
113
-
-
0030217901
-
A second gene for cerulean cataracts maps to the beta-crystallin region on chromosome 22
-
Kramer P., Yount J., Mitchell T.et al. A second gene for cerulean cataracts maps to the beta-crystallin region on chromosome 22. Genomics. 35:1996;39-42.
-
(1996)
Genomics
, vol.35
, pp. 39-42
-
-
Kramer, P.1
Yount, J.2
Mitchell, T.3
-
114
-
-
0030217901
-
A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22
-
Kramer P., Yount J., Mitchell T.et al. A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22. Genomics. 35:1996;539-542.
-
(1996)
Genomics
, vol.35
, pp. 539-542
-
-
Kramer, P.1
Yount, J.2
Mitchell, T.3
-
116
-
-
0014366685
-
Intralenticular hemorrhage following discision of congenital cataract
-
Kurz G.H., Einaugler R.B. Intralenticular hemorrhage following discision of congenital cataract. Am J Ophthalmol. 66:1966;1163-1165.
-
(1966)
Am J Ophthalmol
, vol.66
, pp. 1163-1165
-
-
Kurz, G.H.1
Einaugler, R.B.2
-
118
-
-
0242495393
-
Anatomy and embryology of the lens
-
T.D. Duane, & E.A. Jaeger. Philadelphia: JB Lippincott
-
Lance O. anatomy and embryology of the lens. Duane T.D., Jaeger E.A. Duane's Clinical Ophthalmology, Vol.1. 1988;1-8 JB Lippincott, Philadelphia.
-
(1988)
Duane's Clinical Ophthalmology, Vol.1
, pp. 1-8
-
-
Lance, O.1
-
119
-
-
0027278456
-
The oculocerebrorenal syndrome of Lowe
-
Lavin C.W., McKeown C.A. The oculocerebrorenal syndrome of Lowe. Int Ophthalmol Clin. 33:1993;179-191.
-
(1993)
Int Ophthalmol Clin
, vol.33
, pp. 179-191
-
-
Lavin, C.W.1
McKeown, C.A.2
-
120
-
-
0025190711
-
Mapping X-linked ophthalmic diseases. IV. Provisional assignment of the locus for X-linked congenital cataracts and microcornea (the Nance- Horan syndrome) to Xp22.2-p22.3
-
; discussion 120-1
-
Lewis R.A., Nussbaum R.L., Stambolian D. Mapping X-linked ophthalmic diseases. IV. Provisional assignment of the locus for X-linked congenital cataracts and microcornea (the Nance- Horan syndrome) to Xp22.2-p22.3. Ophthalmology. 97:1990;110-120. ; discussion 120-1.
-
(1990)
Ophthalmology
, vol.97
, pp. 110-120
-
-
Lewis, R.A.1
Nussbaum, R.L.2
Stambolian, D.3
-
121
-
-
0242663765
-
Uber kongenitale Formanomalien der Linse
-
Lisch K. Uber kongenitale Formanomalien der Linse. Arch Ophthalmol. 157:1956;287-293.
-
(1956)
Arch Ophthalmol
, vol.157
, pp. 287-293
-
-
Lisch, K.1
-
122
-
-
0242412055
-
The eyes in mongolism
-
Lower R. The eyes in mongolism. Br J Ophthalmol. 33:1949;529-533.
-
(1949)
Br J Ophthalmol
, vol.33
, pp. 529-533
-
-
Lower, R.1
-
123
-
-
0023131304
-
A locus for a human hereditary cataract is closely linked to the gamma-crystallin gene family
-
Lubsen N.H., Renwick J.H., Tsui L.C.et al. A locus for a human hereditary cataract is closely linked to the gamma-crystallin gene family. Proc Natl Acad Sci USA. 84:1987;489-492.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 489-492
-
-
Lubsen, N.H.1
Renwick, J.H.2
Tsui, L.C.3
-
124
-
-
0026570323
-
Autosomal dominant congenital cataract; Linkage relations; Clinical and genetic heterogeneity
-
Lund A.M., Eiberg H., Rosenberg T., Warburg M. Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity. Clin Genet. 41:1992;65-69.
-
(1992)
Clin Genet
, vol.41
, pp. 65-69
-
-
Lund, A.M.1
Eiberg, H.2
Rosenberg, T.3
Warburg, M.4
-
125
-
-
0026950656
-
A case of invasion of the hyaloid artery into the lens
-
Machida H, Watanabe I: [A case of invasion of the hyaloid artery into the lens]. Nippon Ganka Gakkai Zasshi 96:1483-6, 1992.
-
(1992)
Nippon Ganka Gakkai Zasshi
, vol.96
, pp. 1483-1486
-
-
Machida, H.1
Watanabe, I.2
-
126
-
-
0030978852
-
A new locus for dominant zonular pulverulent cataract, on chromosome 13
-
Mackay D., Ionides A., Berry V.et al. A new locus for dominant zonular pulverulent cataract, on chromosome 13. Am J Hum Genet. 60:1997;1474-1478.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1474-1478
-
-
Mackay, D.1
Ionides, A.2
Berry, V.3
-
127
-
-
0034241549
-
High-frequency ultrasonography findings in persistent hyperplastic primary vitreous
-
Mackeen L.D., Nischal K.K., Lam W.C., Levin A.V. High-frequency ultrasonography findings in persistent hyperplastic primary vitreous. J AAPOS. 4:2000;217-224.
-
(2000)
J AAPOS
, vol.4
, pp. 217-224
-
-
Mackeen, L.D.1
Nischal, K.K.2
Lam, W.C.3
Levin, A.V.4
-
128
-
-
0003839201
-
-
London: Longman, Orme, Brown, Green and Longman, ed 4
-
Mackenzie W: A practical treatise on the disease of the eye. London: Longman, Orme, Brown, Green and Longman, 1854, ed 4, p 757.
-
(1854)
A Practical Treatise on the Disease of the Eye
, pp. 757
-
-
Mackenzie, W.1
-
129
-
-
0016186547
-
An unusual case of congenital presence of blood in the lens
-
Madroszkiewicz M. An unusual case of congenital presence of blood in the lens. Ophthalmologica. 168:1974;462-464.
-
(1974)
Ophthalmologica
, vol.168
, pp. 462-464
-
-
Madroszkiewicz, M.1
-
130
-
-
0017519645
-
A new case of congenital presence of blood in the lens (authors transl)
-
Madroszkiewiczowie M, Madroszkiewiczowie A: [A new case of congenital presence of blood in the lens (authors transl)]. Klin Oczna 47:347-8, 1977.
-
(1977)
Klin Oczna
, vol.47
, pp. 347-348
-
-
Madroszkiewiczowie, M.1
Madroszkiewiczowie, A.2
-
131
-
-
0242663764
-
Posterior lenticonus
-
Makley T.A. Posterior lenticonus. Am J Ophthalmol. 39:1955;308-312.
-
(1955)
Am J Ophthalmol
, vol.39
, pp. 308-312
-
-
Makley, T.A.1
-
134
-
-
0024334955
-
Autosomal dominant congenital cataract. Morphology and genetic mapping
-
Marner E., Rosenberg T., Eiberg H. Autosomal dominant congenital cataract. Morphology and genetic mapping. Acta Ophthalmol (Copenh). 67:1989;151-158.
-
(1989)
Acta Ophthalmol (Copenh)
, vol.67
, pp. 151-158
-
-
Marner, E.1
Rosenberg, T.2
Eiberg, H.3
-
135
-
-
0242579750
-
Lenticonus posterior
-
Marsh E.J. Lenticonus posterior. Arch Ophthalmol. 8:1932;804-820.
-
(1932)
Arch Ophthalmol
, vol.8
, pp. 804-820
-
-
Marsh, E.J.1
-
136
-
-
0242495392
-
Slit-lamp study of posterior lenticonus
-
Marsh E.J. Slit-lamp study of posterior lenticonus. Arch Ophthalmol. 56:1927;128-136.
-
(1927)
Arch Ophthalmol
, vol.56
, pp. 128-136
-
-
Marsh, E.J.1
-
139
-
-
0003040653
-
Congenital cataracts
-
W.A. Renie. Boston: Toronto, Little, Brown and Company
-
Merin S. Congenital cataracts. Renie W.A. Goldberg's genetic and metabolic eye disease. 1986;369-387 Toronto, Little, Brown and Company, Boston.
-
(1986)
Goldberg's Genetic and Metabolic Eye Disease
, pp. 369-387
-
-
Merin, S.1
-
140
-
-
0015150458
-
Hypoglycemia and infantile cataract
-
Merin S., Crawford J.S. Hypoglycemia and infantile cataract. Arch Ophthalmol. 86:1971;495-498.
-
(1971)
Arch Ophthalmol
, vol.86
, pp. 495-498
-
-
Merin, S.1
Crawford, J.S.2
-
141
-
-
0002206887
-
Ein Fall von Lenticonus posterior
-
Meyer F. Ein Fall von Lenticonus posterior. Z Prakt Augenheilkd. 12:1888;41-46.
-
(1888)
Z Prakt Augenheilkd
, vol.12
, pp. 41-46
-
-
Meyer, F.1
-
142
-
-
0242495391
-
Beitrag zur Pathologie und pathologischen Ana-tomie des Schicht- und Kapselstares
-
Meyer O. Beitrag zur Pathologie und pathologischen Ana-tomie des Schicht- und Kapselstares. Klin Monatsbl Augenheilkd. 45:1898;540-562.
-
(1898)
Klin Monatsbl Augenheilkd
, vol.45
, pp. 540-562
-
-
Meyer, O.1
-
143
-
-
0029044852
-
Acquired posterior lentiglobus
-
Mohney B.G., Parks M.M. Acquired posterior lentiglobus. Am J Ophthalmol. 120:1995;123-124.
-
(1995)
Am J Ophthalmol
, vol.120
, pp. 123-124
-
-
Mohney, B.G.1
Parks, M.M.2
-
144
-
-
0021347788
-
Autosomal dominant anterior polar cataracts associated with a familial 2;14 translocation
-
Moross T., Vaithilingam S.S., Styles S., Gardner H.A. Autosomal dominant anterior polar cataracts associated with a familial 2;14 translocation. J Med Genet. 21:1984;52-53.
-
(1984)
J Med Genet
, vol.21
, pp. 52-53
-
-
Moross, T.1
Vaithilingam, S.S.2
Styles, S.3
Gardner, H.A.4
-
145
-
-
4243583794
-
Hat der Lenticonus seinen Grund in einer Anomalie der hinteren Linsenfläche?
-
Müller L. Hat der Lenticonus seinen Grund in einer Anomalie der hinteren Linsenfläche? Klin Monatsbl Augenheilkd. 32:1894;178-194.
-
(1894)
Klin Monatsbl Augenheilkd
, vol.32
, pp. 178-194
-
-
Müller, L.1
-
148
-
-
0001583612
-
Seven new pedigrees of hereditary cataracts
-
Nettleship E. Seven new pedigrees of hereditary cataracts. Trans Ophthalmol Soc UK. 29:1909;188-211.
-
(1909)
Trans Ophthalmol Soc UK
, vol.29
, pp. 188-211
-
-
Nettleship, E.1
-
149
-
-
0242579748
-
On heredity in the various forms of cataract
-
Nettleship E. On heredity in the various forms of cataract. Roy Lond Ophth Hosp Rep. 16:1905;179-246.
-
(1905)
Roy Lond Ophth Hosp Rep
, vol.16
, pp. 179-246
-
-
Nettleship, E.1
-
150
-
-
0000699953
-
A peculier form of hereditary congenital cataract
-
Nettleship E., Ogilvie F.M. A peculier form of hereditary congenital cataract. Trans Ophthalmol Soc UK. 26:1906;191-207.
-
(1906)
Trans Ophthalmol Soc UK
, vol.26
, pp. 191-207
-
-
Nettleship, E.1
Ogilvie, F.M.2
-
151
-
-
0025707353
-
Familial congenital cornea guttata with anterior polar cataracts
-
Nucci P. Familial congenital cornea guttata with anterior polar cataracts. Am J Ophthalmol. 109:1990;245.
-
(1990)
Am J Ophthalmol
, vol.109
, pp. 245
-
-
Nucci, P.1
-
152
-
-
0040920369
-
-
OMIM™. Johns Hopkins University, Baltimore, MD. OMIM No: 600897. Date last edited: 9-9-1999
-
Online Mendelian Inheritance in Man, OMIM™. Johns Hopkins University, Baltimore, MD. OMIM No: 600897. Date last edited: 9-9-1999.
-
Online Mendelian Inheritance in Man
-
-
-
153
-
-
0040920369
-
-
OMIM™. Johns Hopkins University, Baltimore, MD. OMIM No: 116200. Date last edited: 11-22-1999
-
Online Mendelian Inheritance in Man, OMIM™. Johns Hopkins University, Baltimore, MD. OMIM No: 116200. Date last edited: 11-22-1999.
-
Online Mendelian Inheritance in Man
-
-
-
154
-
-
0040920369
-
-
OMIM™. Johns Hopkins University, Baltimore, MD. OMIM No: 123680. Date last edited: 7-27-2000
-
Online Mendelian Inheritance in Man, OMIM™. Johns Hopkins University, Baltimore, MD. OMIM No: 123680. Date last edited: 7-27-2000.
-
Online Mendelian Inheritance in Man
-
-
-
155
-
-
0029095859
-
Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12
-
Padma T., Ayyagari R., Murty J.S.et al. Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12. Am J Hum Genet. 57:1995;840-845.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 840-845
-
-
Padma, T.1
Ayyagari, R.2
Murty, J.S.3
-
156
-
-
0019997097
-
Visual results in aphakic children
-
Parks M.M. Visual results in aphakic children. Am J Ophthalmol. 94:1982;441-449.
-
(1982)
Am J Ophthalmol
, vol.94
, pp. 441-449
-
-
Parks, M.M.1
-
157
-
-
0027210392
-
Long-term visual results and complications in children with aphakia. A function of cataract type
-
discussion 840-1
-
Parks M.M., Johnson D.A., Reed G.W. Long-term visual results and complications in children with aphakia. A function of cataract type. Ophthalmology. 100:1993;826-840. discussion 840-1.
-
(1993)
Ophthalmology
, vol.100
, pp. 826-840
-
-
Parks, M.M.1
Johnson, D.A.2
Reed, G.W.3
-
158
-
-
0019503130
-
Congenital cataracts associated with agenesis of the corpus callosum and cerebral dysgenesis: A case report
-
Pollack M.A., Kolbert G.S. Congenital cataracts associated with agenesis of the corpus callosum and cerebral dysgenesis. a case report J Pediatr Ophthalmol Strabismus. 18:1981;6-8.
-
(1981)
J Pediatr Ophthalmol Strabismus
, vol.18
, pp. 6-8
-
-
Pollack, M.A.1
Kolbert, G.S.2
-
159
-
-
0021972363
-
Treatment of persistent hyperplastic primary vitreous
-
Pollard Z.F. Treatment of persistent hyperplastic primary vitreous. J Pediatr Ophthalmol Strabismus. 22:1985;180-183.
-
(1985)
J Pediatr Ophthalmol Strabismus
, vol.22
, pp. 180-183
-
-
Pollard, Z.F.1
-
160
-
-
0020502302
-
Familial bilateral posterior lenticonus
-
Pollard Z.F. Familial bilateral posterior lenticonus. Arch Ophthalmol. 101:1983;1238-1240.
-
(1983)
Arch Ophthalmol
, vol.101
, pp. 1238-1240
-
-
Pollard, Z.F.1
-
162
-
-
0035697326
-
Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract
-
Polyakov A.V., Shagina I.A., Khlebnikova O.V., Evgrafov O.V. Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract. Clin Genet. 60:2001;476-478.
-
(2001)
Clin Genet
, vol.60
, pp. 476-478
-
-
Polyakov, A.V.1
Shagina, I.A.2
Khlebnikova, O.V.3
Evgrafov, O.V.4
-
163
-
-
0242579747
-
Assignment of the human alpha-A-crystallin gene (CRYA1) to chromosome 21
-
Quax-Jeuken Y., Quax W., Van Rens G.et al. Assignment of the human alpha-A-crystallin gene (CRYA1) to chromosome 21. Cytogenet Cell Genet. 40:1985;727-728.
-
(1985)
Cytogenet Cell Genet
, vol.40
, pp. 727-728
-
-
Quax-Jeuken, Y.1
Quax, W.2
Van Rens, G.3
-
164
-
-
0028877411
-
Ocular abnormalities in neurofibromatosis 2
-
Ragge N.K., Baser M.E., Klein J.et al. Ocular abnormalities in neurofibromatosis 2. Am J Ophthalmol. 120:1995;634-641.
-
(1995)
Am J Ophthalmol
, vol.120
, pp. 634-641
-
-
Ragge, N.K.1
Baser, M.E.2
Klein, J.3
-
165
-
-
0018765901
-
Rare association of hyperglycinuria and lenticonus in two members of the same family
-
Reccia R., Magli A., Pignalosa B.et al. Rare association of hyperglycinuria and lenticonus in two members of the same family. Ophthalmologica. 178:1979;131-136.
-
(1979)
Ophthalmologica
, vol.178
, pp. 131-136
-
-
Reccia, R.1
Magli, A.2
Pignalosa, B.3
-
167
-
-
50449115179
-
Persistent hyperplastic primary vitreous
-
Reese A.B. Persistent hyperplastic primary vitreous. Am J Ophthalmol. 40:1955;317-331.
-
(1955)
Am J Ophthalmol
, vol.40
, pp. 317-331
-
-
Reese, A.B.1
-
168
-
-
0001034829
-
Persistence and hyperplasia of the primary vitreous; Retrolental fibroplasia - Two entities
-
Reese A.B. Persistence and hyperplasia of the primary vitreous; retrolental fibroplasia - two entities. Arch Ophthalmol. 41:1949;527-552.
-
(1949)
Arch Ophthalmol
, vol.41
, pp. 527-552
-
-
Reese, A.B.1
-
171
-
-
0002288531
-
Probable linkage between a congenital cataract locus and Duffy blood group locus
-
Renwick S.H., Lawler S.D. Probable linkage between a congenital cataract locus and Duffy blood group locus. Ann Hum Genet. 27:1963;67-84.
-
(1963)
Ann Hum Genet
, vol.27
, pp. 67-84
-
-
Renwick, S.H.1
Lawler, S.D.2
-
172
-
-
0017603542
-
Lens aspiration. A decade in retrospect
-
Rice N.S. Lens aspiration. A decade in retrospect. Trans Ophthalmol Soc UK. 97:1977;48-51.
-
(1977)
Trans Ophthalmol Soc UK
, vol.97
, pp. 48-51
-
-
Rice, N.S.1
-
173
-
-
0014167090
-
Hereditary "ant-egg-cataract"
-
Riise R. Hereditary "ant-egg-cataract" Acta Ophthalmol. 45:1966;341-346.
-
(1966)
Acta Ophthalmol
, vol.45
, pp. 341-346
-
-
Riise, R.1
-
174
-
-
0017888882
-
Pathology of the lens in Downs syndrome
-
Robb R.M., Marchevsky A. Pathology of the lens in Downs syndrome. Arch Ophthalmol. 96:1978;1039-1042.
-
(1978)
Arch Ophthalmol
, vol.96
, pp. 1039-1042
-
-
Robb, R.M.1
Marchevsky, A.2
-
175
-
-
9244251074
-
Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35
-
Rogaev E.I., Rogaeva E.A., Korovaitseva G.I.et al. Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35. Hum Mol Genet. 5:1996;699-703.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 699-703
-
-
Rogaev, E.I.1
Rogaeva, E.A.2
Korovaitseva, G.I.3
-
176
-
-
0028874460
-
Pierre Robin anomalad, maculo-pathy, and autolytic cataract
-
Rogers N.K., Strachan I.M. Pierre Robin anomalad, maculo-pathy, and autolytic cataract. J Pediatr Ophthalmol Strabismus. 32:1995;391-392.
-
(1995)
J Pediatr Ophthalmol Strabismus
, vol.32
, pp. 391-392
-
-
Rogers, N.K.1
Strachan, I.M.2
-
177
-
-
0242495390
-
Coppock cataract and cataracta pulverulenta centralis
-
Rosen E. Coppock cataract and cataracta pulverulenta centralis. Br J Ophthalmol. 29:1945;641-644.
-
(1945)
Br J Ophthalmol
, vol.29
, pp. 641-644
-
-
Rosen, E.1
-
178
-
-
0028328760
-
Anterior polar cataract in two sisters with an unbalanced 3;18 chromosomal translocation
-
Rubin S.E., Nelson L.B., Pletcher B.A. Anterior polar cataract in two sisters with an unbalanced 3;18 chromosomal translocation. Am J Ophthalmol. 117:1994;512-515.
-
(1994)
Am J Ophthalmol
, vol.117
, pp. 512-515
-
-
Rubin, S.E.1
Nelson, L.B.2
Pletcher, B.A.3
-
179
-
-
0034353237
-
Non-syndromic lenticonus a cause of childhood cataract: Evidence for X-Linked inheritance
-
Russell-Eggitt I.M. Non-syndromic lenticonus a cause of childhood cataract. Evidence for X-Linked inheritance Eye. 14:2000;861-863.
-
(2000)
Eye
, vol.14
, pp. 861-863
-
-
Russell-Eggitt, I.M.1
-
180
-
-
0023895786
-
Variable expressivity of autosomal dominant microcornea with cataract
-
Salmon J.F., Wallis C.E., Murray A.D. Variable expressivity of autosomal dominant microcornea with cataract. Arch Ophthalmol. 106:1988;505-510.
-
(1988)
Arch Ophthalmol
, vol.106
, pp. 505-510
-
-
Salmon, J.F.1
Wallis, C.E.2
Murray, A.D.3
-
183
-
-
0025045846
-
The mechanisms of cataract formation
-
Schmitt C., Hockwin O. The mechanisms of cataract formation. J Inherit Metab Dis. 13:1990;501-508.
-
(1990)
J Inherit Metab Dis
, vol.13
, pp. 501-508
-
-
Schmitt, C.1
Hockwin, O.2
-
184
-
-
0018488004
-
Ant-egg cataract. An electron microscopic study
-
Schroder H.D., Nissen S.H. Ant-egg cataract. An electron microscopic study. Acta Ophthalmol (Copenh). 57:1979;435-442.
-
(1979)
Acta Ophthalmol (Copenh)
, vol.57
, pp. 435-442
-
-
Schroder, H.D.1
Nissen, S.H.2
-
185
-
-
0028364446
-
Autosomal dominant congenital cataract. Interocular phenotypic variability
-
Scott M.H., Hejtmancik J.F., Wozencraft L.A.et al. Autosomal dominant congenital cataract. Interocular phenotypic variability. Ophthalmology. 101:1994;866-871.
-
(1994)
Ophthalmology
, vol.101
, pp. 866-871
-
-
Scott, M.H.1
Hejtmancik, J.F.2
Wozencraft, L.A.3
-
186
-
-
0022438404
-
Treatment of congenital cataracts and persistent hyperplastic primary vitreous
-
Scott W.E. Treatment of congenital cataracts and persistent hyperplastic primary vitreous. Trans New Orleans Acad Ophthalmol. 34:1986;461-477.
-
(1986)
Trans New Orleans Acad Ophthalmol
, vol.34
, pp. 461-477
-
-
Scott, W.E.1
-
188
-
-
0027471298
-
A newborn with posterior lenticonus
-
Seidenberg K., Ludwig I.H. A newborn with posterior lenticonus. Am J Ophthalmol. 115:1993;543-544.
-
(1993)
Am J Ophthalmol
, vol.115
, pp. 543-544
-
-
Seidenberg, K.1
Ludwig, I.H.2
-
189
-
-
0031811116
-
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD
-
Semina E.V., Ferrell R.E., Mintz-Hittner H.A.et al. A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nat Genet. 19:1998;167-170.
-
(1998)
Nat Genet
, vol.19
, pp. 167-170
-
-
Semina, E.V.1
Ferrell, R.E.2
Mintz-Hittner, H.A.3
-
190
-
-
0031959735
-
A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant zonular pulverulent cataract, on chromosome 1q
-
Shiels A., Mackay D., Ionides A.et al. A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant zonular pulverulent cataract, on chromosome 1q. Am J Hum Genet. 62:1998;526-532.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 526-532
-
-
Shiels, A.1
Mackay, D.2
Ionides, A.3
-
191
-
-
0030781992
-
A pars plana approach for cataract surgery in posterior lenticonus
-
Simons B.D., Flynn H.W. Jr. A pars plana approach for cataract surgery in posterior lenticonus. Am J Ophthalmol. 124:1997;695-696.
-
(1997)
Am J Ophthalmol
, vol.124
, pp. 695-696
-
-
Simons, B.D.1
Flynn H.W., Jr.2
-
193
-
-
0242663762
-
A pedigree of Doyne's discoid cataract
-
Smith P. A pedigree of Doyne's discoid cataract. Trans Ophthalmol Soc UK. 30:1910;37-42.
-
(1910)
Trans Ophthalmol Soc UK
, vol.30
, pp. 37-42
-
-
Smith, P.1
-
194
-
-
0025772592
-
Spontaneous bilateral lens resorption in a case of Hallermann-Streiff syndrome
-
Soriano JM, Funk J: [Spontaneous bilateral lens resorption in a case of Hallermann-Streiff syndrome]. Klin Monatsbl Augenheilkd 199:195-8, 1991.
-
(1991)
Klin Monatsbl Augenheilkd
, vol.199
, pp. 195-198
-
-
Soriano, J.M.1
Funk, J.2
-
195
-
-
0013831616
-
Fabry's disease. Its ocular manifestations
-
Spaeth G.L., Frost P. Fabry's disease. Its ocular manifestations. Arch Ophthalmol. 74:1965;760-769.
-
(1965)
Arch Ophthalmol
, vol.74
, pp. 760-769
-
-
Spaeth, G.L.1
Frost, P.2
-
196
-
-
0023212948
-
Sticklers syndrome: A study of 12 families
-
Spallone A. Sticklers syndrome. a study of 12 families Br J Ophthalmol. 71:1987;504-509.
-
(1987)
Br J Ophthalmol
, vol.71
, pp. 504-509
-
-
Spallone, A.1
-
197
-
-
0031695178
-
Congenital cataract surgery in children with cataract as an isolated defect and in children with a systemic syndrome: A comparative study
-
Spierer A., Desatnik H., Rosner M., Blumenthal M. Congenital cataract surgery in children with cataract as an isolated defect and in children with a systemic syndrome. a comparative study J Pediatr Ophthalmol Strabismus. 35:1998;281-285.
-
(1998)
J Pediatr Ophthalmol Strabismus
, vol.35
, pp. 281-285
-
-
Spierer, A.1
Desatnik, H.2
Rosner, M.3
Blumenthal, M.4
-
198
-
-
0021014835
-
Study of a form of pulverulent cataract in a large kindred
-
Stabile M., Amoriello A., Capobianco S.et al. Study of a form of pulverulent cataract in a large kindred. J Med Genet. 20:1983;419-421.
-
(1983)
J Med Genet
, vol.20
, pp. 419-421
-
-
Stabile, M.1
Amoriello, A.2
Capobianco, S.3
-
199
-
-
0019754217
-
Surgical management of persistent hyperplastic primary vitreous
-
Stark W.J. Surgical management of persistent hyperplastic primary vitreous. Dev Ophthalmol. 5:1981;115-121.
-
(1981)
Dev Ophthalmol
, vol.5
, pp. 115-121
-
-
Stark, W.J.1
-
200
-
-
0021048430
-
Management of persistent hyperplastic primary vitreous
-
Stark W.J., Fagadau W., Lindsey P.S.et al. Management of persistent hyperplastic primary vitreous. Aust J Ophthalmol. 11:1983;195-200.
-
(1983)
Aust J Ophthalmol
, vol.11
, pp. 195-200
-
-
Stark, W.J.1
Fagadau, W.2
Lindsey, P.S.3
-
202
-
-
13044250483
-
Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene
-
Stephan D.A., Gillanders E., Vanderveen D.et al. Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene. Proc Natl Acad Sci U S A. 96:1999;1008-1012.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 1008-1012
-
-
Stephan, D.A.1
Gillanders, E.2
Vanderveen, D.3
-
204
-
-
0014847702
-
Anterior lenticonus and the Waardenburg syndrome
-
Stevens P.R. Anterior lenticonus and the Waardenburg syndrome. Br J Ophthalmol. 54:1970;621-623.
-
(1970)
Br J Ophthalmol
, vol.54
, pp. 621-623
-
-
Stevens, P.R.1
-
205
-
-
4243339436
-
Normvarianten der Morphologie der kindlichen Linse
-
Stöcklin P. Normvarianten der Morphologie der kindlichen Linse. Graefes Arch Ophthalmol. 158:1957;346-359.
-
(1957)
Graefes Arch Ophthalmol
, vol.158
, pp. 346-359
-
-
Stöcklin, P.1
-
207
-
-
0242663759
-
Zur Klinik und Pathogenese des sogenannten Lenticonus posterior
-
Szily von A. Zur Klinik und Pathogenese des sogenannten Lenticonus posterior. Klin Monatsbl Augenheilkd. 77:1926;845.
-
(1926)
Klin Monatsbl Augenheilkd
, vol.77
, pp. 845
-
-
Szily von, A.1
-
208
-
-
0031909743
-
The Doyne Lecture. Congenital cataract: The history, the nature and the practice
-
Taylor D. The Doyne Lecture. Congenital cataract. the history, the nature and the practice Eye. 12:1998;9-36.
-
(1998)
Eye
, vol.12
, pp. 9-36
-
-
Taylor, D.1
-
209
-
-
0021896445
-
Anterior dislocation of the pyramidal part of a congenital cataract
-
Thomas R., Gopal K.S., George J.A. Anterior dislocation of the pyramidal part of a congenital cataract. Indian J Ophthalmol. 33:1985;51-52.
-
(1985)
Indian J Ophthalmol
, vol.33
, pp. 51-52
-
-
Thomas, R.1
Gopal, K.S.2
George, J.A.3
-
210
-
-
0024344836
-
Familial congenital cornea guttata with anterior polar cataracts
-
Traboulsi E.I., Weinberg R.J. Familial congenital cornea guttata with anterior polar cataracts. Am J Ophthalmol. 108:1989;123-125.
-
(1989)
Am J Ophthalmol
, vol.108
, pp. 123-125
-
-
Traboulsi, E.I.1
Weinberg, R.J.2
-
211
-
-
0022522190
-
Pathogenesis of cataracts in patients with Lowes syndrome
-
Tripathi R.C., Cibis G.W., Tripathi B.J. Pathogenesis of cataracts in patients with Lowes syndrome. Ophthalmology. 93:1986;1046-1051.
-
(1986)
Ophthalmology
, vol.93
, pp. 1046-1051
-
-
Tripathi, R.C.1
Cibis, G.W.2
Tripathi, B.J.3
-
212
-
-
0242663760
-
Lenticonus posterior
-
Tyson H.H. Lenticonus posterior. Arch Ophthalmol. 57:1928;38-50.
-
(1928)
Arch Ophthalmol
, vol.57
, pp. 38-50
-
-
Tyson, H.H.1
-
213
-
-
0022552287
-
Haemorrhage in the lens: Spontaneous occurrence in congenital cataract
-
Unoki K., Nakao K., Ohba N. Haemorrhage in the lens. spontaneous occurrence in congenital cataract Br J Ophthalmol. 70:1986;593-595.
-
(1986)
Br J Ophthalmol
, vol.70
, pp. 593-595
-
-
Unoki, K.1
Nakao, K.2
Ohba, N.3
-
214
-
-
0035125622
-
A novel form of central pouchlike cataract, with sutural opacities, maps to chromosome 15q21-22
-
Vanita Singh J.R., Sarhadi V.K.et al. A novel form of central pouchlike cataract, with sutural opacities, maps to chromosome 15q21-22. Am J Hum Genet. 68:2001;509-514.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 509-514
-
-
Vanita Singh, J.R.1
Sarhadi, V.K.2
-
215
-
-
0015130618
-
Possible traumatic origin of posterior lenticonus in a patient with congenital posterior lens opacity of familial character
-
Vittone P: [Possible traumatic origin of posterior lenticonus in a patient with congenital posterior lens opacity of familial character]. Minerva Oftalmol 13:113-6, 1971.
-
(1971)
Minerva Oftalmol
, vol.13
, pp. 113-116
-
-
Vittone, P.1
-
217
-
-
0242495389
-
Ueber lenticonus axialis und periphericus posterior
-
Vogt A. Ueber lenticonus axialis und periphericus posterior. Klin Monatsbl Augenheilkd. 77:1926;709-710.
-
(1926)
Klin Monatsbl Augenheilkd
, vol.77
, pp. 709-710
-
-
Vogt, A.1
-
218
-
-
0242579743
-
Die Spezifität angeborener und erworbener Starformen für die einzelnen Linsenzonen
-
Vogt A. Die Spezifität angeborener und erworbener Starformen für die einzelnen Linsenzonen. Graefes Arch Ophthalmol. 108:1922;219-228.
-
(1922)
Graefes Arch Ophthalmol
, vol.108
, pp. 219-228
-
-
Vogt, A.1
-
219
-
-
0242495387
-
Die vordere axiale Embryonalkatarakt der menschlichen Linse
-
Vogt A. Die vordere axiale Embryonalkatarakt der menschlichen Linse. Z Augenheilkd. 41:1919;125-137.
-
(1919)
Z Augenheilkd
, vol.41
, pp. 125-137
-
-
Vogt, A.1
-
220
-
-
0242579744
-
Uber excentrische Bildung des Linsenkernes und die Histologie des Lenticonus posterior
-
Von Hess C. Uber excentrische Bildung des Linsenkernes und die Histologie des Lenticonus posterior. Dtsch Ophthalmol Ges. 301:1986;301.
-
(1986)
Dtsch Ophthalmol Ges
, vol.301
, pp. 301
-
-
Von Hess, C.1
-
221
-
-
0034021246
-
Linkage analysis in an autosomal dominant zonular nuclear pulverulent congenital cataract, mapped to chromosome 13q11-13
-
Watts P., Rees M., Clarke A.et al. Linkage analysis in an autosomal dominant zonular nuclear pulverulent congenital cataract, mapped to chromosome 13q11-13. Eye. 14:2000;172-175.
-
(2000)
Eye
, vol.14
, pp. 172-175
-
-
Watts, P.1
Rees, M.2
Clarke, A.3
-
222
-
-
0014384766
-
Persistent hyperplastic primary vitreous with resorption of the lens
-
Wegener J.K., Sogaard H. Persistent hyperplastic primary vitreous with resorption of the lens. Acta Ophthalmol (Copenh). 46:1968;171-175.
-
(1968)
Acta Ophthalmol (Copenh)
, vol.46
, pp. 171-175
-
-
Wegener, J.K.1
Sogaard, H.2
-
225
-
-
0013821552
-
Spontaneous cataract reabsorption in Hallermann-Streiff Syndrome
-
Wolter J.R., Jones D.H. Spontaneous cataract reabsorption in Hallermann-Streiff Syndrome. Ophthalmologica. 150:1965;401-408.
-
(1965)
Ophthalmologica
, vol.150
, pp. 401-408
-
-
Wolter, J.R.1
Jones, D.H.2
-
226
-
-
0033663027
-
Expression of connective tissue growth factor (CTGF) mRNA in plaques of human anterior subcapsular cataracts and membranes of posterior capsule opacification
-
Wunderlich K., Pech M., Eberle A.N.et al. Expression of connective tissue growth factor (CTGF) mRNA in plaques of human anterior subcapsular cataracts and membranes of posterior capsule opacification. Curr Eye Res. 21:2000;627-636.
-
(2000)
Curr Eye Res
, vol.21
, pp. 627-636
-
-
Wunderlich, K.1
Pech, M.2
Eberle, A.N.3
-
227
-
-
0033922770
-
An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12
-
Yamada K., Tomita H., Yoshiura K.et al. An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12. Eur J Hum Genet. 8:2000;535-539.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 535-539
-
-
Yamada, K.1
Tomita, H.2
Yoshiura, K.3
-
228
-
-
0023939213
-
Family with aniridia, microcornea, and spontaneously reabsorbed cataract
-
Yamamoto Y., Hayasaka S., Setogawa T. Family with aniridia, microcornea, and spontaneously reabsorbed cataract. Arch Ophthalmol. 106:1988;502-504.
-
(1988)
Arch Ophthalmol
, vol.106
, pp. 502-504
-
-
Yamamoto, Y.1
Hayasaka, S.2
Setogawa, T.3
-
229
-
-
0025244925
-
Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome
-
Zhu D., Alcorn D.M., Antonarakis S.E.et al. Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome. Hum Genet. 86:1990;54-58.
-
(1990)
Hum Genet
, vol.86
, pp. 54-58
-
-
Zhu, D.1
Alcorn, D.M.2
Antonarakis, S.E.3
-
230
-
-
85031201090
-
Klinische Beobachtungen. Mehrere seltene Fälle von congenitaler Kataract
-
Zirm E. Klinische Beobachtungen. Mehrere seltene Fälle von congenitaler Kataract. Klin Monatsbl Augenheilkd. 30:1892;5-25.
-
(1892)
Klin Monatsbl Augenheilkd
, vol.30
, pp. 5-25
-
-
Zirm, E.1
|