-
1
-
-
0031436787
-
Clinical experience of trabeculotomy for the surgical treatment of aniridic glaucoma
-
Adachi M, Dickens CJ, Hetherington J, Hoskins HD, Iwach AG, Wong PC, Nguyen N & Ma AS (1997): Clinical experience of trabeculotomy for the surgical treatment of aniridic glaucoma. Ophthalmology 104: 2121-2125.
-
(1997)
Ophthalmology
, vol.104
, pp. 2121-2125
-
-
Adachi, M.1
Dickens, C.J.2
Hetherington, J.3
Hoskins, H.D.4
Iwach, A.G.5
Wong, P.C.6
Nguyen, N.7
Ma, A.S.8
-
2
-
-
34447623215
-
Outcomes of Boston keratoprosthesis in aniridia: A retrospective multicenter study
-
Akpek EK, Harissi-Dagher M, Petrarca R, Butrus SI, Pineda R II, Aquavella JV & Dohlman CH (2007): Outcomes of Boston keratoprosthesis in aniridia: A retrospective multicenter study. Am J Ophthalmol 144: 227-231.
-
(2007)
Am J Ophthalmol
, vol.144
, pp. 227-231
-
-
Akpek, E.K.1
Harissi-Dagher, M.2
Petrarca, R.3
Butrus, S.I.4
Pineda, R.5
Aquavella, J.V.6
Dohlman, C.H.7
-
3
-
-
0000066383
-
The cause and treatment of poor vision in aniridia
-
Alger LG (1945): The cause and treatment of poor vision in aniridia. Am J Ophthalmol 28: 730-735.
-
(1945)
Am J Ophthalmol
, vol.28
, pp. 730-735
-
-
Alger, L.G.1
-
4
-
-
0033362155
-
Missense mutation in the alternative splice region of the pax6 gene in eye anomalies
-
Azuma N, Yamaguchi Y, Handa H, Hayakawa M, Kanai A & Yamada M (1999): Missense mutation in the alternative splice region of the pax6 gene in eye anomalies. Am J Hum Genet 65: 656-663.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 656-663
-
-
Azuma, N.1
Yamaguchi, Y.2
Handa, H.3
Hayakawa, M.4
Kanai, A.5
Yamada, M.6
-
5
-
-
0036805779
-
Pax6 heterozygous eyes show defects in chamber angle differentiation that are associated with a wide spectrum of other anterior eye segment abnormalities
-
Baulmanna DC, Ohlmanna A, Flugel-Kocha C, Goswamib S, Cveklb A & Tamm ER (2002): Pax6 heterozygous eyes show defects in chamber angle differentiation that are associated with a wide spectrum of other anterior eye segment abnormalities. Mech Dev 118: 3-17.
-
(2002)
Mech Dev
, vol.118
, pp. 3-17
-
-
Baulmanna, D.C.1
Ohlmanna, A.2
Flugel-Kocha, C.3
Goswamib, S.4
Cveklb, A.5
Tamm, E.R.6
-
6
-
-
0023007234
-
An alternative hypothesis for iris maldevelopment (aniridia)
-
Beauchamp GR & Meisler DM (1986): An alternative hypothesis for iris maldevelopment (aniridia). J Pediatr Ophthalmol Strabismus 23: 281-283.
-
(1986)
J Pediatr Ophthalmol Strabismus
, vol.23
, pp. 281-283
-
-
Beauchamp, G.R.1
Meisler, D.M.2
-
7
-
-
0018353052
-
Filtering surgery in children: Barriers to success
-
Beauchamp GR & Parks MM (1979): Filtering surgery in children: barriers to success. Ophthalmology 86: 170-180.
-
(1979)
Ophthalmology
, vol.86
, pp. 170-180
-
-
Beauchamp, G.R.1
Parks, M.M.2
-
8
-
-
1242316165
-
Markedly increased central corneal thickness: An unrecognized finding in congenital aniridia
-
Brandt JD, Casuso LA & Budenz DL (2004): Markedly increased central corneal thickness: An unrecognized finding in congenital aniridia. Am J Ophthalmol 137: 348-350.
-
(2004)
Am J Ophthalmol
, vol.137
, pp. 348-350
-
-
Brandt, J.D.1
Casuso, L.A.2
Budenz, D.L.3
-
9
-
-
17144430529
-
Combination of WAGR and potocki-snaffer contiguous deletion syndromes in a patient with an 11p11.2-p14 deletion
-
Bremond-Gignac D, Crolla JA, Copin H et al. (2005): Combination of WAGR and potocki-snaffer contiguous deletion syndromes in a patient with an 11p11.2-p14 deletion. Eur J Hum Genet 13: 409-413.
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 409-413
-
-
Bremond-Gignac, D.1
Crolla, J.A.2
Copin, H.3
-
11
-
-
55449116920
-
Wilms'nephroblastoma and congenital renal diseases in the case reports of the Istituto Provinciale di Protezione ed Assistenza dell'Infanzia di Milano
-
Brusa P & Torricelli C (1953): Wilms'nephroblastoma and congenital renal diseases in the case reports of the Istituto Provinciale di Protezione ed Assistenza dell'Infanzia di Milano. Minerva Pediatr 30: 5.
-
(1953)
Minerva Pediatr
, vol.30
, pp. 5
-
-
Brusa, P.1
Torricelli, C.2
-
12
-
-
0035169725
-
Prosthetic iris implantation for congenital, traumatic, or functional iris deficiencies
-
Burk SE, Da Mata AP, Snyder ME, Cionni RJ, Cohen JS & Osher RH (2001): Prosthetic iris implantation for congenital, traumatic, or functional iris deficiencies. J Cataract Refract Surg 27: 1732-1740.
-
(2001)
J Cataract Refract Surg
, vol.27
, pp. 1732-1740
-
-
Burk, S.E.1
Da Mata, A.P.2
Snyder, M.E.3
Cionni, R.J.4
Cohen, J.S.5
Osher, R.H.6
-
13
-
-
0345893112
-
Lamellar intrastromal corneal tattoo for treating iris defects (artificial iris)
-
Burris TE, Holmes-Higgin DK & Silvestrini TA (1999): Lamellar intrastromal corneal tattoo for treating iris defects (artificial iris). Cornea 18: 498-499.
-
(1999)
Cornea
, vol.18
, pp. 498-499
-
-
Burris, T.E.1
Holmes-Higgin, D.K.2
Silvestrini, T.A.3
-
14
-
-
0036845710
-
Regulation of corneal keratin-12 gene expression by the human Krüppel-like transcription factor 6
-
Chiambaretta F, Blanchon L, Rabier B, Kao WWY, Liu JJ, Dastugue B, Rigal D & Sapin V (2002): Regulation of corneal keratin-12 gene expression by the human Krüppel-like transcription factor 6. Invest Ophthalmol Vis Sci 43: 3422-3429.
-
(2002)
Invest Ophthalmol Vis Sci
, vol.43
, pp. 3422-3429
-
-
Chiambaretta, F.1
Blanchon, L.2
Rabier, B.3
Kao, W.W.Y.4
Liu, J.J.5
Dastugue, B.6
Rigal, D.7
Sapin, V.8
-
17
-
-
2142652984
-
Corneal development, limbal stem cell function, and corneal epithelial cell migration in the Pax6 +/-mouse
-
Collinson JM, Chanas SA, Hill RE & West JD (2004): Corneal development, limbal stem cell function, and corneal epithelial cell migration in the Pax6 +/-mouse. Invest Ophthalmol Vis Sci 45: 1101-1108.
-
(2004)
Invest Ophthalmol Vis Sci
, vol.45
, pp. 1101-1108
-
-
Collinson, J.M.1
Chanas, S.A.2
Hill, R.E.3
West, J.D.4
-
18
-
-
38449111238
-
Two siblings with 46 XY DSD, congenital adrenal hypoplasia, aniridia, craniofacial, and skeletal abnormalities and intrauterine growth retardation: A new syndrome?
-
Coman DJ, White SM & Amor DJ (2007): Two siblings with 46 XY DSD, congenital adrenal hypoplasia, aniridia, craniofacial, and skeletal abnormalities and intrauterine growth retardation: A new syndrome? Am J Med Genet A 143: 2085-2088.
-
(2007)
Am J Med Genet A
, vol.143
, pp. 2085-2088
-
-
Coman, D.J.1
White, S.M.2
Amor, D.J.3
-
19
-
-
0025374503
-
Aniridia and deafness: An inherited disorder
-
Courtney-Harris RA & Phil MM (1990): Aniridia and deafness: an inherited disorder. J Laryngol Otol 104: 419-420.
-
(1990)
J Laryngol Otol
, vol.104
, pp. 419-420
-
-
Courtney-Harris, R.G.1
Phil, M.M.2
-
20
-
-
0036844718
-
Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia
-
Crolla JA & Van Heyningen V (2002): Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia. Am J Hum Genet 71: 1138-1149.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1138-1149
-
-
Crolla, J.A.1
Van Heyningen, V.2
-
22
-
-
0029014879
-
Retinal detachment and giant retinal tears in aniridia
-
Dowler JG, Lyons CJ & Cooling RJ (1995): Retinal detachment and giant retinal tears in aniridia. Eye 9: 268-270.
-
(1995)
Eye
, vol.9
, pp. 268-270
-
-
Dowler, J.G.1
Lyons, C.J.2
Cooling, R.J.3
-
23
-
-
0028096639
-
Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing
-
Epstein JA, Glaser T, Cai J, Jepeal L, Walton DS & Maas RL (1994a): Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing. Genes Dev 8: 2022-2034.
-
(1994)
Genes Dev
, vol.8
, pp. 2022-2034
-
-
Epstein, J.A.1
Glaser, T.2
Cai, J.3
Jepeal, L.4
Walton, D.S.5
Maas, R.L.6
-
24
-
-
0028239775
-
Entification of A Pax paired domain recognition sequence and evidence for dna-dependent conformational changes
-
Epstein J, Cai J, Glaser T, Jepeal L & Maas R (1994b): Entification of A Pax paired domain recognition sequence and evidence for dna-dependent conformational changes. J Biol Chem 269: 8355-8361.
-
(1994)
J Biol Chem
, vol.269
, pp. 8355-8361
-
-
Epstein, J.1
Cai, J.2
Glaser, T.3
Jepeal, L.4
Maas, R.5
-
25
-
-
0026740023
-
Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization
-
Fantes JA, Bickmore WA, Fletcher JM, Ballesta F, Hanson M & van Heyningen V (1992): Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization. Am J Hum Genet 51: 1286-1294.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1286-1294
-
-
Fantes, J.A.1
Bickmore, W.A.2
Fletcher, J.M.3
Ballesta, F.4
Hanson, M.5
van Heyningen, V.6
-
26
-
-
0028058986
-
Human haploinsufficiency - One for sorrow, two for joy
-
Fisher E & Scambler P (1994): Human haploinsufficiency - one for sorrow, two for joy. Nat Genet 7: 5-7.
-
(1994)
Nat Genet
, vol.7
, pp. 5-7
-
-
Fisher, E.1
Scambler, P.2
-
27
-
-
0029678243
-
The master control gene for morphogenesis and evolution of the eye
-
Gehring WJ (1996): The master control gene for morphogenesis and evolution of the eye. Genes Cells 1: 11-15.
-
(1996)
Genes Cells
, vol.1
, pp. 11-15
-
-
Gehring, W.J.1
-
28
-
-
0001261865
-
Aniridia, cerebellar ataxia and oligophrenia in siblings
-
Gillespie FD (1965): Aniridia, cerebellar ataxia and oligophrenia in siblings. Arch Ophthalmol 73: 338-341.
-
(1965)
Arch Ophthalmol
, vol.73
, pp. 338-341
-
-
Gillespie, F.D.1
-
29
-
-
0026949405
-
Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene
-
Glaser T, Walton DS & Maas R (1992): Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene. Nat Genet 2: 232-239.
-
(1992)
Nat Genet
, vol.2
, pp. 232-239
-
-
Glaser, T.1
Walton, D.S.2
Maas, R.3
-
30
-
-
0028074973
-
PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects
-
Erratum in Nat Genet 8: 203
-
Glaser T, Jepeal L, Edwards JG, Young SR, Favor J & Maas RL (1994): PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. Nat Genet 7: 463-471, Erratum in Nat Genet 8: 203.
-
(1994)
Nat Genet
, vol.7
, pp. 463-471
-
-
Glaser, T.1
Jepeal, L.2
Edwards, J.G.3
Young, S.R.4
Favor, J.5
Maas, R.L.6
-
31
-
-
0029741248
-
Recurrent keratopathy after penetrating keratoplasty for aniridia
-
Gomes JA, Eagle RC, Gomes AK, Rapuano CJ, Cohen EJ & Laibson PR (1996): Recurrent keratopathy after penetrating keratoplasty for aniridia. Cornea 15: 457-462.
-
(1996)
Cornea
, vol.15
, pp. 457-462
-
-
Gomes, J.A.1
Eagle, R.C.2
Gomes, A.K.3
Rapuano, C.J.4
Cohen, E.J.5
Laibson, P.R.6
-
32
-
-
0016307327
-
Progressive changes in the angle in congenital aniridia, with development of glaucoma
-
Grant WM & Walton DS (1974): Progressive changes in the angle in congenital aniridia, with development of glaucoma. Trans Am Ophthalmol Soc 72: 207-228.
-
(1974)
Trans Am Ophthalmol Soc
, vol.72
, pp. 207-228
-
-
Grant, W.M.1
Walton, D.S.2
-
34
-
-
0032899711
-
Missense mutations in the most ancient residues of PAX6 paired domain underlie a spectrum of human congenital eye malformations
-
Hanson I, Churchill A, Love J, Axton R, Moore T, Clarke M, Meire F & van Heyningen V (1999): Missense mutations in the most ancient residues of PAX6 paired domain underlie a spectrum of human congenital eye malformations. Hum Mol Genet 6: 165-172.
-
(1999)
Hum Mol Genet
, vol.6
, pp. 165-172
-
-
Hanson, I.1
Churchill, A.2
Love, J.3
Axton, R.4
Moore, T.5
Clarke, M.6
Meire, F.7
van Heyningen, V.8
-
35
-
-
0037226810
-
Management of aniridic keratopathy with keratolimbal allograft: A limbal stem cell transplantation technique
-
Holland EJ, Djalilian AR & Schwartz GS (2003): Management of aniridic keratopathy with keratolimbal allograft: A limbal stem cell transplantation technique. Ophthalmology 110: 125-130.
-
(2003)
Ophthalmology
, vol.110
, pp. 125-130
-
-
Holland, E.J.1
Djalilian, A.R.2
Schwartz, G.S.3
-
36
-
-
46449089221
-
Clinical pathological study of the anterior lens capsule abnormalities in familial congenital aniridia with cataract
-
Hou ZQ, Hao YS, Wang W, Ma ZZ, Zhong YF & Song SJ (2005): Clinical pathological study of the anterior lens capsule abnormalities in familial congenital aniridia with cataract. Beijing Da Xue Xue Bao 37: 494-497.
-
(2005)
Beijing Da Xue Xue Bao
, vol.37
, pp. 494-497
-
-
Hou, Z.Q.1
Hao, Y.S.2
Wang, W.3
Ma, Z.Z.4
Zhong, Y.F.5
Song, S.J.6
-
37
-
-
0029029812
-
Aniridia: Recent achievements in paediatric practice
-
IvanRv I (1995): Aniridia: recent achievements in paediatric practice. Eur J Pediatr 154: 795-800.
-
(1995)
Eur J Pediatr
, vol.154
, pp. 795-800
-
-
Ivanov, I.1
-
38
-
-
24944538017
-
Association of aniridia and dry eyes
-
Jastaneiah S & Al-Rajhi AA (2005): Association of aniridia and dry eyes. Ophthalmology 112: 1535-1540.
-
(2005)
Ophthalmology
, vol.112
, pp. 1535-1540
-
-
Jastaneiah, S.1
Al-Rajhi, A.A.2
-
39
-
-
0025125041
-
11p13 deletion, Wilm's tumor and aniridia: Unusual genetic and non ocular and ocular features of three cases
-
Jotterand V, Boisjoly HM, Harnois C, Bigonesse P, Laframboise R, Gagné R & St-Pierre A (1990): 11p13 deletion, Wilm's tumor and aniridia: Unusual genetic and non ocular and ocular features of three cases. Br J Ophthalmol 74: 568-570.
-
(1990)
Br J Ophthalmol
, vol.74
, pp. 568-570
-
-
Jotterand, V.1
Boisjoly, H.M.2
Harnois, C.3
Bigonesse, P.4
Laframboise, R.5
Gagné, R.6
St-Pierre, A.7
-
40
-
-
0027532492
-
Results of penetrating keratoplasty in aniridia
-
Kremer I, Rajpal RK, Rapuano CJ, Cohen EJ & Laibson PR (1993): Results of penetrating keratoplasty in aniridia. Am J Ophthalmol 115: 317-320.
-
(1993)
Am J Ophthalmol
, vol.115
, pp. 317-320
-
-
Kremer, I.1
Rajpal, R.K.2
Rapuano, C.J.3
Cohen, E.J.4
Laibson, P.R.5
-
41
-
-
0034801999
-
Limbus transplantation for reconstruction of the ocular surface
-
Kruse FE & Reinhard T (2001): Limbus transplantation for reconstruction of the ocular surface. Ophthalmologe 98: 818-831.
-
(2001)
Ophthalmologe
, vol.98
, pp. 818-831
-
-
Kruse, F.E.1
Reinhard, T.2
-
42
-
-
34248181062
-
Cell surface glycoconjugate abnormalities and corneal epithelial wound healing in the pax6 +/-mouse model of aniridia-related keratopathy
-
Kucerova R, Ou J, Lawson D, Leiper LJ & Collinson JM (2006): Cell surface glycoconjugate abnormalities and corneal epithelial wound healing in the pax6 +/-mouse model of aniridia-related keratopathy. Invest Ophthalmol Vis Sci 47: 5276-5282.
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 5276-5282
-
-
Kucerova, R.1
Ou, J.2
Lawson, D.3
Leiper, L.J.4
Collinson, J.M.5
-
43
-
-
0022794655
-
Aniridia, congenital glaucoma and hydrocephalus in a male infant with ring chromosome 6
-
Levin H, Ritch R, Borathur R, Dunn MW, Teekhasaenee C, Margons S (1986): Aniridia, congenital glaucoma and hydrocephalus in a male infant with ring chromosome 6. Am J Med Genet 25: 281-287.
-
(1986)
Am J Med Genet
, vol.25
, pp. 281-287
-
-
Levin, H.1
Ritch, R.2
Borathur, R.3
Dunn, M.W.4
Teekhasaenee, C.5
Margons, S.6
-
44
-
-
0027374508
-
Cornea-specific expression of K12 keratin during mouse development
-
Liu CY, Zhu G, Westerhausen-Larson A, Converse R, Kao CW, Sun TT & Kao WW (1993): Cornea-specific expression of K12 keratin during mouse development. Curr Eye Res 12: 963-974.
-
(1993)
Curr Eye Res
, vol.12
, pp. 963-974
-
-
Liu, C.Y.1
Zhu, G.2
Westerhausen-Larson, A.3
Converse, R.4
Kao, C.W.5
Sun, T.T.6
Kao, W.W.7
-
46
-
-
0030918127
-
Mitomycin C-augmented trabeculectomy in refractory congenital glaucoma
-
Mandal AK, Walton DS, John T & Jayagandan A (1997): Mitomycin C-augmented trabeculectomy in refractory congenital glaucoma. Ophthalmology 104: 996-1001.
-
(1997)
Ophthalmology
, vol.104
, pp. 996-1001
-
-
Mandal, A.K.1
Walton, D.S.2
John, T.3
Jayagandan, A.4
-
47
-
-
0020518916
-
Congenital aniridia: A histopathologic study of the anterior segment in children
-
Margo CE (1983)A Congenital aniridia: a histopathologic study of the anterior segment in children. J Pediatr Ophthalmol Strabismus 20: 192-198.
-
(1983)
J Pediatr Ophthalmol Strabismus
, vol.20
, pp. 192-198
-
-
Margo, C.E.1
-
48
-
-
0028294152
-
Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins
-
Martha A, Ferrell RE, Mintz-Hittner H, Lyons LA & Saunders GF (1994): Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins. Am J Hum Genet 54: 801-811.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 801-811
-
-
Martha, A.1
Ferrell, R.E.2
Mintz-Hittner, H.3
Lyons, L.A.4
Saunders, G.F.5
-
49
-
-
0024435866
-
Ambiguous genitalia, gonadoblastoma, aniridia and mental retardation with deletion of chromosome 11
-
Martinez-Mora J, Audi L, Toran N, Isnard R, Castellvi A, Perez Iribarne M & Egozcue J (1989): Ambiguous genitalia, gonadoblastoma, aniridia and mental retardation with deletion of chromosome 11. J Urol 142: 1298-1300.
-
(1989)
J Urol
, vol.142
, pp. 1298-1300
-
-
Martinez-Mora, J.1
Audi, L.2
Toran, N.3
Isnard, R.4
Castellvi, A.5
Perez Iribarne, M.6
Egozcue, J.7
-
50
-
-
0036062035
-
Phacoemulsification and endocapsular implantation of an artificial iris intraocular lens in traumatic cataract and aniridia
-
Mavrikakis I & Casey JM (2002): Phacoemulsification and endocapsular implantation of an artificial iris intraocular lens in traumatic cataract and aniridia. J Cataract Refract Surg 28: 1088-1091.
-
(2002)
J Cataract Refract Surg
, vol.28
, pp. 1088-1091
-
-
Mavrikakis, I.1
Casey, J.M.2
-
51
-
-
0342421744
-
Aniridia
-
In: Buyse ML (ed) Dover Mass: Center for Birth Defects Information Services
-
Mets MB & Cross HE (1990): Aniridia. In: Buyse ML (ed) Birth defect encyclopaedia. Dover Mass: Center for Birth Defects Information Services 144-145.
-
(1990)
Birth Defect Encyclopaedia
, pp. 144-145
-
-
Mets, M.B.1
Cross, H.E.2
-
52
-
-
22744445535
-
Aniridia and optic nerve hypoplasia
-
McCulley TJ, Mayer K, Dahr SS, Simpson J & Holland EJ (2005): Aniridia and optic nerve hypoplasia. Eye 19: 762-764.
-
(2005)
Eye
, vol.19
, pp. 762-764
-
-
McCulley, T.J.1
Mayer, K.2
Dahr, S.S.3
Simpson, J.4
Holland, E.J.5
-
53
-
-
78651152965
-
Association of Wilm's Tumor with aniridia, hemihypertrophy and other congential malformations
-
Miller RW, Fraumeni JF Jr, Manning MD (1964): Association of Wilm's Tumor with aniridia, hemihypertrophy and other congential malformations. N Eng J Med 270: 922-927.
-
(1964)
N Eng J Med
, vol.270
, pp. 922-927
-
-
Miller, R.W.1
Fraumeni Jr., J.F.2
Manning, M.D.3
-
54
-
-
0016793877
-
A familial syndrome of aniridia and absence of the patella
-
Mirkinson AE & Mirkinson NK (1975): A familial syndrome of aniridia and absence of the patella. Birth Defects Orig Artic Ser 11: 129-131.
-
(1975)
Birth Defects Orig Artic Ser
, vol.11
, pp. 129-131
-
-
Mirkinson, A.E.1
Mirkinson, N.K.2
-
55
-
-
0029097307
-
Mutation of the PAX6 gene in patients with autosomal dominant keratitis
-
Mirzayans F, Pearce WG, MacDonald M & Walter MA (1995): Mutation of the PAX6 gene in patients with autosomal dominant keratitis. Am J Hum Genet 57: 539-548.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 539-548
-
-
Mirzayans, F.1
Pearce, W.G.2
MacDonald, M.3
Walter, M.A.4
-
56
-
-
0037127214
-
Matrix metalloproteinase gelatinase B (MMP-9) coordinates and effects epithelial regeneration
-
Mohan R, Chintala SK, Jung JC et al. (2002): Matrix metalloproteinase gelatinase B (MMP-9) coordinates and effects epithelial regeneration. J Biol Chem 277: 2065-2072.
-
(2002)
J Biol Chem
, vol.277
, pp. 2065-2072
-
-
Mohan, R.1
Chintala, S.K.2
Jung, J.C.3
-
57
-
-
0025903372
-
Clinical experience with the Molteno implant in advanced infantile glaucoma
-
Munoz M, Tomey KF, Traverso C, Day SH & Senft SH (1991): Clinical experience with the Molteno implant in advanced infantile glaucoma. J Pediatr Ophthalmol Strabismus 28: 68-72.
-
(1991)
J Pediatr Ophthalmol Strabismus
, vol.28
, pp. 68-72
-
-
Munoz, M.1
Tomey, K.F.2
Traverso, C.3
Day, S.H.4
Senft, S.H.5
-
58
-
-
0021240429
-
Aniridia. A review
-
Nelson LB, Spaeth GL, Nowinski TS, Margo CE & Jackson L (1984): Aniridia. A review. Surv Ophthalmol 28: 621-642.
-
(1984)
Surv Ophthalmol
, vol.28
, pp. 621-642
-
-
Nelson, L.B.1
Spaeth, G.L.2
Nowinski, T.S.3
Margo, C.E.4
Jackson, L.5
-
59
-
-
0029125267
-
Ocular surface abnormalities in aniridia
-
Nishida K, Kinoshita S, Ohashi Y, Kuwayama Y & Yamamoto S (1995): Ocular surface abnormalities in aniridia. Am J Ophthalmol 120: 368-375.
-
(1995)
Am J Ophthalmol
, vol.120
, pp. 368-375
-
-
Nishida, K.1
Kinoshita, S.2
Ohashi, Y.3
Kuwayama, Y.4
Yamamoto, S.5
-
60
-
-
0032979930
-
PAX6 expression in the developing human eye
-
Nishina S, Kohsaka S, Yamaguchi Y, Handa H, Kawakami A, Fujisawa H & Azuma N (1999): PAX6 expression in the developing human eye. Br J Ophthalmol 83: 723-727.
-
(1999)
Br J Ophthalmol
, vol.83
, pp. 723-727
-
-
Nishina, S.1
Kohsaka, S.2
Yamaguchi, Y.3
Handa, H.4
Kawakami, A.5
Fujisawa, H.6
Azuma, N.7
-
61
-
-
0033814285
-
Results of filtering surgery in young patients with aniridia
-
Okada K, Mishima HK, Masumoto M, Tsumamoto Y, Tsukamoto H & Takamatsu M (2000): Results of filtering surgery in young patients with aniridia. Hiroshima J Med Sci 49: 135-138.
-
(2000)
Hiroshima J Med Sci
, vol.49
, pp. 135-138
-
-
Okada, K.1
Mishima, H.K.2
Masumoto, M.3
Tsumamoto, Y.4
Tsukamoto, H.5
Takamatsu, M.6
-
62
-
-
0032744776
-
Cataract surgery combined with implantation of an artificial iris
-
Osher RH & Burk SE (1999): Cataract surgery combined with implantation of an artificial iris. J Cataract Refract Surg 25: 1540-1547.
-
(1999)
J Cataract Refract Surg
, vol.25
, pp. 1540-1547
-
-
Osher, R.H.1
Burk, S.E.2
-
63
-
-
0033867411
-
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations
-
Perveen R, Lloyd IC, Clayton-Smith J et al. (2000): Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations. Invest Ophthalmol Vis Sci 41: 2456-2460.
-
(2000)
Invest Ophthalmol Vis Sci
, vol.41
, pp. 2456-2460
-
-
Perveen, R.1
Lloyd, I.C.2
Clayton-Smith, J.3
-
64
-
-
0033146715
-
Intermediate-term results of endoscopic diode laser cyclophotocoagulation for pediatric glaucoma
-
Plager DA & Neely DE (1999): Intermediate-term results of endoscopic diode laser cyclophotocoagulation for pediatric glaucoma. J AAPOS 3: 131-137.
-
(1999)
J AAPOS
, vol.3
, pp. 131-137
-
-
Plager, D.A.1
Neely, D.E.2
-
65
-
-
0037406767
-
Corneal abnormalities in Pax6+/-small eye mice mimic human aniridia-related keratopathy
-
Ramaesh T, Collinson JM, Ramaesh K, Kaufman MH, West JD & Dhillon B (2003): Corneal abnormalities in Pax6+/-small eye mice mimic human aniridia-related keratopathy. Invest Ophthalmol Vis Sci 44: 1871-1878.
-
(2003)
Invest Ophthalmol Vis Sci
, vol.44
, pp. 1871-1878
-
-
Ramaesh, T.1
Collinson, J.M.2
Ramaesh, K.3
Kaufman, M.H.4
West, J.D.5
Dhillon, B.6
-
66
-
-
0028007312
-
Bei traumtischer aniridie
-
[Iris black diaphragm intraocular lenses in traumatic aniridia]
-
Reinhard T, Sundmacher R & Althaus C (1994): Bei traumtischer aniridie [Iris black diaphragm intraocular lenses in traumatic aniridia]. Klin Monatsbl Augenheilkd 205: 196-200.
-
(1994)
Klin Monatsbl Augenheilkd
, vol.205
, pp. 196-200
-
-
Reinhard, T.1
Sundmacher, R.2
Althaus, C.3
-
67
-
-
0034019943
-
Black diaphragm aniridia intraocular lens for congenital aniridia: Long-term follow-up
-
Reinhard T, Engelhardt S & Sundmacher R (2000): Black diaphragm aniridia intraocular lens for congenital aniridia: Long-term follow-up. J Cataract Refract Surg 26: 375-381.
-
(2000)
J Cataract Refract Surg
, vol.26
, pp. 375-381
-
-
Reinhard, T.1
Engelhardt, S.2
Sundmacher, R.3
-
68
-
-
0022856010
-
Bilateral aniridia with Marfan's syndrome and dental anomalies - A new association
-
Sachdev MS, Sood NN, Kumar H & Ghose S (1986): Bilateral aniridia with Marfan's syndrome and dental anomalies - a new association. Jpn J Ophthalmol 30: 360-366.
-
(1986)
Jpn J Ophthalmol
, vol.30
, pp. 360-366
-
-
Sachdev, M.S.1
Sood, N.N.2
Kumar, H.3
Ghose, S.4
-
69
-
-
0037351439
-
Thinning of the anterior capsule associated with congenital aniridia
-
Schneider S, Osher RH, Burk SE, Lutz TB & Montione R (2003): Thinning of the anterior capsule associated with congenital aniridia. J Cataract Refract Surg 29: 523-525.
-
(2003)
J Cataract Refract Surg
, vol.29
, pp. 523-525
-
-
Schneider, S.1
Osher, R.H.2
Burk, S.E.3
Lutz, T.B.4
Montione, R.5
-
70
-
-
0035115979
-
Impression cytology-proven corneal stem cell deficiency in patients after surgeries involving the limbus
-
Sridhar MS, Vemuganti GK, Bansal AK & Rao GN (2001): Impression cytology-proven corneal stem cell deficiency in patients after surgeries involving the limbus. Cornea 20: 145-148.
-
(2001)
Cornea
, vol.20
, pp. 145-148
-
-
Sridhar, M.S.1
Vemuganti, G.K.2
Bansal, A.K.3
Rao, G.N.4
-
71
-
-
0028492625
-
Black diaphragm intraocular lens in congenital aniridia
-
Sundmacher T, Reinhard T & Althaus C (1994): Black diaphragm intraocular lens in congenital aniridia. Ger J Ophthalmol 3: 197-201.
-
(1994)
Ger J Ophthalmol
, vol.3
, pp. 197-201
-
-
Sundmacher, T.1
Reinhard, T.2
Althaus, C.3
-
72
-
-
0032738435
-
Black iris-diaphragm intraocular lens for aniridia and aphakia
-
Tanzer DJ & Smith RE (1999): Black iris-diaphragm intraocular lens for aniridia and aphakia. J Cataract Refract Surg 25: 1548-1551.
-
(1999)
J Cataract Refract Surg
, vol.25
, pp. 1548-1551
-
-
Tanzer, D.J.1
Smith, R.E.2
-
74
-
-
33845506247
-
Ocular finding in Gillespie-like syndrome: Association with a new PAX6 mutation
-
Ticho BH (2006): Ocular finding in GiAlespie-like syndrome: association with a new PAX6 mutation. Ophthalmic Genet 27: 145-149.
-
(2006)
Ophthalmic Genet
, vol.27
, pp. 145-149
-
-
Ticho, B.H.1
-
75
-
-
0037361801
-
The influence of keratoplasty on visual prognosis in aniridia: A historical review of one large family
-
Tiller AM, Odenthal MT, Verbraak FD & Gortzak-Moorstein N (2003): The influence of keratoplasty on visual prognosis in aniridia: A historical review of one large family. Cornea 22: 105-110.
-
(2003)
Cornea
, vol.22
, pp. 105-110
-
-
Tiller, A.M.1
Odenthal, M.T.2
Verbraak, F.D.3
Gortzak-Moorstein, N.4
-
76
-
-
0026315044
-
Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region
-
Ton CC, Hirvonen H, Miwa H et al. (1991): Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region. Cell 67: 1059-1074.
-
(1991)
Cell
, vol.67
, pp. 1059-1074
-
-
Ton, C.C.1
Hirvonen, H.2
Miwa, H.3
-
77
-
-
40849135619
-
Aniridia with preserved visual function: A report of four cases with no mutations in Pax6
-
Traboulsi EI, Ellison J, Sears J, Maumenee IH, Avallone J & Mohney BG (2008): Aniridia with preserved Aisual function: a report of four cases with no mutations in Pax6. Am J Ophthalmol 145: 760-764.
-
(2008)
Am J Ophthalmol
, vol.145
, pp. 760-764
-
-
Traboulsi, E.I.1
Ellison, J.2
Sears, J.3
Maumenee, I.H.4
Avallone, J.5
Mohney, B.G.6
-
78
-
-
0032142803
-
Effects of PAX6 mutations on retinal function: An electroretinographic study
-
Tremblay F, Gupta SK, De Becker I, Guernsey DL & Neumann PE (1998): Effects of PAX6 mutations on retinal function: An electroretinographic study. Am J Ophthalmol 126: 211-218.
-
(1998)
Am J Ophthalmol
, vol.126
, pp. 211-218
-
-
Tremblay, F.1
Gupta, S.K.2
De Becker, I.3
Guernsey, D.L.4
Neumann, P.E.5
-
79
-
-
0030029671
-
Comparison of protein kinase C subtype expression between normal and aniridic human ocular surfaces: Implications for limbal stem cell dysfunction in aniridia
-
Tseng SC & Li DQ (1996): Comparison of protein kinase C subtype expression between normal and aniridic human ocular surfaces: implications for limbal stem cell dysfunction in aniridia. Cornea 15: 168-178.
-
(1996)
Cornea
, vol.15
, pp. 168-178
-
-
Tseng, S.C.1
Li, D.Q.2
-
80
-
-
0031952807
-
Amniotic membrane transplantation with or without limbal allografts for corneal surface reconstruction in patients with limbal stem cell deficiency
-
Tseng SC, Prabhasawat P, Barton K, Gray T & Meller D (1998): Amniotic membrane transplantation with or without limbal allografts for corneal surface reconstruction in patients with limbal stem cell deficiency. Arch Ophthalmol 116: 431-441.
-
(1998)
Arch Ophthalmol
, vol.116
, pp. 431-441
-
-
Tseng, S.C.1
Prabhasawat, P.2
Barton, K.3
Gray, T.4
Meller, D.5
-
82
-
-
8144227539
-
Ocular and nonocular findings in patients with aniridia
-
Valenzuela A & Cline RA (2004): Ocular and nonocular findings in patients with aniridia. Can J Ophthalmol 39: 632-638.
-
(2004)
Can J Ophthalmol
, vol.39
, pp. 632-638
-
-
Valenzuela, A.1
Cline, R.A.2
-
83
-
-
0030980905
-
Coloboma, mental retardation, hypogonadism and obesity: Critical review of the so-called Biemond syndrome type 2, updated nosology and delineation of three new syndromes
-
Verloes A, Temple IK, Bonnet S & Bottani A (1997): Coloboma, mental retardation, hypogonadism and obesity: Critical review of the so-called Biemond syndrome type 2, updated nosology and delineation of three new syndromes. Am J Med Genet 69: 370-379.
-
(1997)
Am J Med Genet
, vol.69
, pp. 370-379
-
-
Verloes, A.1
Temple, I.K.2
Bonnet, S.3
Bottani, A.4
-
84
-
-
0037300234
-
Screening for PAX6 gene mutations is consistent with haploinsufficiency as the main mechanism leading to various ocular defects
-
Vincent MC, Pujo AL, Oliver D & Calvas P (2003): Screening for PAX6 gene mutations is consistent with haploinsufficiency as the main mechanism leading to various ocular defects. Eur J Hum Genet 11: 163-169.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 163-169
-
-
Vincent, M.C.1
Pujo, A.L.2
Oliver, D.3
Calvas, P.4
-
85
-
-
0031771357
-
Long-term outcome of cyclocryotherapy for refractory pediatric glaucoma
-
Wagle NS, Freedman SF, Buckley EG, Davis JS & Biglan AW (1998): Long-term outcome of cyclocryotherapy for refractory pediatric glaucoma. Ophthalmology 105: 1921-1927.
-
(1998)
Ophthalmology
, vol.105
, pp. 1921-1927
-
-
Wagle, N.S.1
Freedman, S.F.2
Buckley, E.G.3
Davis, J.S.4
Biglan, A.W.5
-
86
-
-
0031893396
-
Surgical results of secondary glaucomas in childhood
-
Wallace DK, Plager DA, Snyder SK, Raiesdana A, Helveston EM & Ellis FD (1998): Surgical results of secondary glaucomas in childhood. Ophthalmology 105: 101-111.
-
(1998)
Ophthalmology
, vol.105
, pp. 101-111
-
-
Wallace, D.K.1
Plager, D.A.2
Snyder, S.K.3
Raiesdana, A.4
Helveston, E.M.5
Ellis, F.D.6
-
87
-
-
0026340588
-
Pax-6, a murine paired box gene, is expressed in the developing CNS
-
Walther C & Gruss P (1991): Pax-6, a murine paired box gene, is expressed in the developing CNS. Development 113: 1435-1449.
-
(1991)
Development
, vol.113
, pp. 1435-1449
-
-
Walther, C.1
Gruss, P.2
-
88
-
-
32044440323
-
Central corneal thickness in patients with congenital aniridia
-
Whitson JT, Liang C, Godfrey DG, Petroll WM, Cavanagh HD, Patel D, Fellman RL & Starita RJ (2005): Central corneal thickness in patients with congenital aniridia. Eye Contact Lens 31: 221-224.
-
(2005)
Eye Contact Lens
, vol.31
, pp. 221-224
-
-
Whitson, J.T.1
Liang, C.2
Godfrey, D.G.3
Petroll, W.M.4
Cavanagh, H.D.5
Patel, D.6
Fellman, R.L.7
Starita, R.J.8
-
89
-
-
0026559383
-
The results of glaucoma surgery in aniridia
-
Wiggins RE & Tomey KF (1992): The results of glaucoma surgery in aniridia. Arch Ophthalmol 110: 503-505.
-
(1992)
Arch Ophthalmol
, vol.110
, pp. 503-505
-
-
Wiggins, R.E.1
Tomey, K.F.2
-
90
-
-
0026223883
-
Abnormalities of ERG in congenital aniridia
-
Wu L, Ma Q, Chen Y, Wu DZ & Luo T (1991): Abnormalities of ERG in congenital aniridia. Yan Ke Xue Bao 7: 151-152, 119.
-
(1991)
Yan Ke Xue Bao
, vol.7
, pp. 151-152
-
-
Wu, L.1
Ma, Q.2
Chen, Y.3
Wu, D.Z.4
Luo, T.5
-
91
-
-
0028919759
-
Crystal structure of a paired domain-DNA complex at 2.5 A resolution reveals structural basis for Pax developmental mutations
-
Xu W, Rould MA, Jun S, Desplan C & Pabo CO (1995): Crystal structure of a paired domain-DNA complex at 2.5 A resolution reveals structural basis for Pax developmental mutations. Cell 80: 639-650.
-
(1995)
Cell
, vol.80
, pp. 639-650
-
-
Xu, W.1
Rould, M.A.2
Jun, S.3
Desplan, C.4
Pabo, C.O.5
-
92
-
-
0024207534
-
Aniridia, ectopia lentis, abnormal upper incisors and mental retardation - An autosomal recessive syndrome
-
Zamzam A, Sheriff SMM & Phillips CI (1988): Aniridia, ectopia lentis, abnormal upper incisors and mental retardation - an autosomal recessive syndrome. Jpn J Ophthalmol 32: 375-378.
-
(1988)
Jpn J Ophthalmol
, vol.32
, pp. 375-378
-
-
Zamzam, A.1
Sheriff, S.M.M.2
Phillips, C.I.3
|