-
1
-
-
0019175901
-
Hypertrophy of the retinal pigment epithelium associated with Gardner's syndrome
-
1 Blair NP, Trempe CL: Hypertrophy of the retinal pigment epithelium associated with Gardner's syndrome. Am J Ophthalmol 1980, 90:661-667.
-
(1980)
Am J Ophthalmol
, vol.90
, pp. 661-667
-
-
Blair, N.P.1
Trempe, C.L.2
-
2
-
-
0023141362
-
Prevalence and importance of pigmented ocular fundus lesions in Gardner's syndrome
-
2 Traboulsi El, Krush AJ, Gardner EJ, Booker SV, Offerhaus GJA, Yardley JH, et al.: Prevalence and importance of pigmented ocular fundus lesions in Gardner's syndrome. N Engl J Med 1987, 316:661-667.
-
(1987)
N Engl J Med
, vol.316
, pp. 661-667
-
-
Traboulsi, E.1
Krush, A.J.2
Gardner, E.J.3
Booker, S.V.4
Offerhaus, G.J.A.5
Yardley, J.H.6
-
3
-
-
0030712337
-
Diagnostic value of fundus examination in familial adenomatous polyposis
-
3 Tiret A, Sartral-Taiel M, Tiret E, Laroche L: Diagnostic value of fundus examination in familial adenomatous polyposis. Br J Ophthalmol 1997, 81:755-758.
-
(1997)
Br J Ophthalmol
, vol.81
, pp. 755-758
-
-
Tiret, A.1
Sartral-Taiel, M.2
Tiret, E.3
Laroche, L.4
-
4
-
-
0028091260
-
Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposis
-
4 Hodgson SV, Bishop D T, Jay B: Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposis. J Med Genet 1994, 1:55-58.
-
(1994)
J Med Genet
, vol.1
, pp. 55-58
-
-
Hodgson, S.V.1
Bishop, D.T.2
Jay, B.3
-
5
-
-
0027769633
-
Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients
-
5 Olschwang S, Tiret A, Laurent-Puig L, Muleris M, Parc R, Thomas G: Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients. Cell 1993, 75:959-968.
-
(1993)
Cell
, vol.75
, pp. 959-968
-
-
Olschwang, S.1
Tiret, A.2
Laurent-Puig, L.3
Muleris, M.4
Parc, R.5
Thomas, G.6
-
6
-
-
0028905406
-
Familial adenomatous polyposis: Desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444
-
6 Caspari R, Olschwang S, Friedl W, Mandl M, Boisson C, Bsker T, et al.: Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444. Hum Mol Genet 1995, 4:337-340.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 337-340
-
-
Caspari, R.1
Olschwang, S.2
Friedl, W.3
Mandl, M.4
Boisson, C.5
Bsker, T.6
-
7
-
-
0029078623
-
Genotype-phenotype correlations of new causative APC gene mutations in patients with familial adenomatous polyposis
-
7 Bunyan DJ, Shea-Simonds J, Reck AC, Finnis D, Eccles DM: Genotype-phenotype correlations of new causative APC gene mutations in patients with familial adenomatous polyposis. J Med Genet 1995, 32:728-731.
-
(1995)
J Med Genet
, vol.32
, pp. 728-731
-
-
Bunyan, D.J.1
Shea-Simonds, J.2
Reck, A.C.3
Finnis, D.4
Eccles, D.M.5
-
8
-
-
0027468256
-
Pigmented fundus lesions in a preterm infant with familial adenomatous polyposis
-
8 Aiello LP, Traboulsi EI: Pigmented fundus lesions in a preterm infant with familial adenomatous polyposis. Arch Ophthalmol 1993, 111:302-303.
-
(1993)
Arch Ophthalmol
, vol.111
, pp. 302-303
-
-
Aiello, L.P.1
Traboulsi, E.I.2
-
9
-
-
0023888797
-
Congenital hypertrophy of the retinal pigment epithelium as a marker for familial adenomatous polyposis
-
9 Berk T, Cohen Z, McLeod RS, Parker JA: Congenital hypertrophy of the retinal pigment epithelium as a marker for familial adenomatous polyposis. Dis Colon Rectum 1988, 31:253-257.
-
(1988)
Dis Colon Rectum
, vol.31
, pp. 253-257
-
-
Berk, T.1
Cohen, Z.2
McLeod, R.S.3
Parker, J.A.4
-
10
-
-
0025079508
-
Pigmented lesions of the retinal pigment epithelium and familial adenomatous polyposis
-
10 Polkinghorne PJ, Ritchie S, Neale K, Schoeppner G, Thomson JPS, Jay BS: Pigmented lesions of the retinal pigment epithelium and familial adenomatous polyposis. Eye 1990, 4:216-221.
-
(1990)
Eye
, vol.4
, pp. 216-221
-
-
Polkinghorne, P.J.1
Ritchie, S.2
Neale, K.3
Schoeppner, G.4
Thomson, J.P.S.5
Jay, B.S.6
-
11
-
-
0029990987
-
Frequency of congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis
-
11 Olea JL, Mateos JM, Llompart A, Obrador A: Frequency of congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Acta Ophthalmol Scand 1996, 74:48-50.
-
(1996)
Acta Ophthalmol Scand
, vol.74
, pp. 48-50
-
-
Olea, J.L.1
Mateos, J.M.2
Llompart, A.3
Obrador, A.4
-
12
-
-
0032076198
-
Ophthalmic and genetic screening in pedigrees with familial adenomatous polyposis
-
12 Ruhswurm I, Zehetmayer M, Dejaco C, Wolf B, Karner-Hanusch J: Ophthalmic and genetic screening in pedigrees with familial adenomatous polyposis. Am J Ophthalmol 1998, 125:680-686.
-
(1998)
Am J Ophthalmol
, vol.125
, pp. 680-686
-
-
Ruhswurm, I.1
Zehetmayer, M.2
Dejaco, C.3
Wolf, B.4
Karner-Hanusch, J.5
-
13
-
-
0026474813
-
Lack of association among typical congenital hypertrophy of the retinal pigment epithelium, adenomatous polyposis, and Gardner syndrome
-
13 Shields JA, Shields CL, Shah PG, Pastore DJ, Imperiale SM Jr: Lack of association among typical congenital hypertrophy of the retinal pigment epithelium, adenomatous polyposis, and Gardner syndrome. Ophthalmology 1992, 99:1709-1713.
-
(1992)
Ophthalmology
, vol.99
, pp. 1709-1713
-
-
Shields, J.A.1
Shields, C.L.2
Shah, P.G.3
Pastore, D.J.4
Imperiale S.M., Jr.5
-
14
-
-
0028217385
-
Congenital hypertrophy of the retinal pigment epithelium associated with familial adenomatous polyposis
-
14 Santos A, Morales L, Hernandez-Quintela E, Jimenez-Sierra JM, Villalobos JJ, Panduro A: Congenital hypertrophy of the retinal pigment epithelium associated with familial adenomatous polyposis. Retina 1994, 14:6-9.
-
(1994)
Retina
, vol.14
, pp. 6-9
-
-
Santos, A.1
Morales, L.2
Hernandez-Quintela, E.3
Jimenez-Sierra, J.M.4
Villalobos, J.J.5
Panduro, A.6
-
15
-
-
0031403621
-
Ocular findings in familial adenomatous polyposis
-
15 Gelisken O, Yÿcel A, Gÿler K, Zorluoglu A: Ocular findings in familial adenomatous polyposis. Int Ophthalmol 1997, 21:205-208.
-
(1997)
Int Ophthalmol
, vol.21
, pp. 205-208
-
-
Gelisken, O.1
Yÿcel, A.2
Gÿler, K.3
Zorluoglu, A.4
-
16
-
-
0028224552
-
Changes in the retinal pigment epithelium close to retinal vessels in familial adenomatous polyposis
-
16 Schmidt D, Jung CE, Wolff G: Changes in the retinal pigment epithelium close to retinal vessels in familial adenomatous polyposis. Graefes Arch Clin Exp Ophthalmol 1994, 232:96-102.
-
(1994)
Graefes Arch Clin Exp Ophthalmol
, vol.232
, pp. 96-102
-
-
Schmidt, D.1
Jung, C.E.2
Wolff, G.3
-
17
-
-
0025048916
-
A clinico-pathologic study of the eyes in familial adenomatous polyposis with extracolonic manifestations (Gardner's syndrome)
-
17 Traboulsi EL, Murphy SF, De La Cruz ZC, Maumenee IH, Green R: A clinico-pathologic study of the eyes in familial adenomatous polyposis with extracolonic manifestations (Gardner's syndrome). Am J Ophthalmol 1990, 110: 550-561.
-
(1990)
Am J Ophthalmol
, vol.110
, pp. 550-561
-
-
Traboulsi, E.L.1
Murphy, S.F.2
De La Cruz, Z.C.3
Maumenee, I.H.4
Green, R.5
-
18
-
-
0030449558
-
Pigmented ocular fundus lesions and APC mutations in familial adenomatous polyposis
-
18 Traboulsi EI, Apostolides J, Giardello FM, Krush AJ, Booker SV, Hamilton SR, Maumenee Hussels IE: Pigmented ocular fundus lesions and APC mutations in familial adenomatous polyposis. Ophthalmic Genet 1996, 17:167-174.
-
(1996)
Ophthalmic Genet
, vol.17
, pp. 167-174
-
-
Traboulsi, E.I.1
Apostolides, J.2
Giardello, F.M.3
Krush, A.J.4
Booker, S.V.5
Hamilton, S.R.6
Maumenee Hussels, I.E.7
-
19
-
-
0026591237
-
A histopathologic study of the pigmented fundus lesions in familial adenomatous polyposis
-
19 Kasner L, Traboulsi EI, De La Cruz Z, Green WR: A histopathologic study of the pigmented fundus lesions in familial adenomatous polyposis. Retina 1992, 12:35-42.
-
(1992)
Retina
, vol.12
, pp. 35-42
-
-
Kasner, L.1
Traboulsi, E.I.2
De la Cruz, Z.3
Green, W.R.4
-
20
-
-
0025366072
-
Histopathological features of congenital fundus lesions in familial adenomatous polyposis
-
20 Parker JA, Kalnins VI, Deck JHN, Cohen Z, Berk T, Sullen JB, et al.: Histopathological features of congenital fundus lesions in familial adenomatous polyposis. Can J Ophthalmol 1990, 25:159-163.
-
(1990)
Can J Ophthalmol
, vol.25
, pp. 159-163
-
-
Parker, J.A.1
Kalnins, V.I.2
Deck, J.H.N.3
Cohen, Z.4
Berk, T.5
Sullen, J.B.6
-
21
-
-
0026705159
-
Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial adenomatous polyposis
-
21 Morton DG, Gibson J, Macdonald F, Brown R, Haydon J, Cullen R, et al.: Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial adenomatous polyposis. Br J Surg 1992, 79:689-693.
-
(1992)
Br J Surg
, vol.79
, pp. 689-693
-
-
Morton, D.G.1
Gibson, J.2
Macdonald, F.3
Brown, R.4
Haydon, J.5
Cullen, R.6
-
22
-
-
84907112782
-
Incidence and significance of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial adenomatous polyposis coli (FAPC)
-
22 Moore AT, Maher ER, Koch DJ, Charles SJ: Incidence and significance of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial adenomatous polyposis coli (FAPC). Ophthalmic Paediatr Genet 1992, 13: 67-71.
-
(1992)
Ophthalmic Paediatr Genet
, vol.13
, pp. 67-71
-
-
Moore, A.T.1
Maher, E.R.2
Koch, D.J.3
Charles, S.J.4
-
23
-
-
10544228516
-
Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis: Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutations
-
23 Valanzano R, Cama A, Volpe R, Curia MC, Mencucci R, Palmirotta R, et al.: Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis: novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutations. Cancer 1996, 78:2400-2410.
-
(1996)
Cancer
, vol.78
, pp. 2400-2410
-
-
Valanzano, R.1
Cama, A.2
Volpe, R.3
Curia, M.C.4
Mencucci, R.5
Palmirotta, R.6
-
24
-
-
0028998378
-
Familial variation in retinal pigmentation in adenomatous polyposis
-
24 Parker JA, Berk T, Bapat BV: Familial variation in retinal pigmentation in adenomatous polyposis. Can J Ophthalmol 1995, 30:138-141.
-
(1995)
Can J Ophthalmol
, vol.30
, pp. 138-141
-
-
Parker, J.A.1
Berk, T.2
Bapat, B.V.3
-
25
-
-
0025666452
-
Predictive value of congenital hypertrophy of the retinal pigment epithelium as a clinical marker for familiat adenomatous polyposis
-
25 Heyen F, Jagelman DG, Romania A, Zakov ZN, Lavery IC, Fazio VW, McGannon E: Predictive value of congenital hypertrophy of the retinal pigment epithelium as a clinical marker for familiat adenomatous polyposis. Dis Colon Rectum 1990, 33:1003-1008.
-
(1990)
Dis Colon Rectum
, vol.33
, pp. 1003-1008
-
-
Heyen, F.1
Jagelman, D.G.2
Romania, A.3
Zakov, Z.N.4
Lavery, I.C.5
Fazio, V.W.6
McGannon, E.7
-
26
-
-
0025938038
-
Identification and characterization of the familial adenomatous polyposis coli gene
-
26 Groden J, Thliveris A, Samowitz W, Carlson M, Gelbert L, Albertsen H, et al.: Identification and characterization of the familial adenomatous polyposis coli gene. Cell 1991, 66:589-600.
-
(1991)
Cell
, vol.66
, pp. 589-600
-
-
Groden, J.1
Thliveris, A.2
Samowitz, W.3
Carlson, M.4
Gelbert, L.5
Albertsen, H.6
-
27
-
-
0025817880
-
Identification of FAP locus genes from chromosome 5q21
-
27 Kinzler KW, Nilbert MC, Su LK, Vogelstein B, Bryan TM, Levy DB, et al.: Identification of FAP locus genes from chromosome 5q21. Science 1991, 253:661-665.
-
(1991)
Science
, vol.253
, pp. 661-665
-
-
Kinzler, K.W.1
Nilbert, M.C.2
Su, L.K.3
Vogelstein, B.4
Bryan, T.M.5
Levy, D.B.6
-
28
-
-
0027330412
-
Predictive diagnosis in familial adenomatous polyposis: Evaluation of molecular genetic and ophthalmologic methods
-
28 Caspari R, Friedl W, Boker T, Augustin A, Mandl M, Jaeger K, et al.: Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods. Z Gastroenterol 1993, 31:646-652.
-
(1993)
Z Gastroenterol
, vol.31
, pp. 646-652
-
-
Caspari, R.1
Friedl, W.2
Boker, T.3
Augustin, A.4
Mandl, M.5
Jaeger, K.6
-
29
-
-
0028117866
-
Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis
-
29 Wallis YL, Macdonald F, Hulten M, Morton JEV, McKeown CM, Neoptolemos J, et al.: Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis. Hum Genet 1994, 94:543-54B.
-
(1994)
Hum Genet
, vol.94
-
-
Wallis, Y.L.1
Macdonald, F.2
Hulten, M.3
Morton, J.E.V.4
McKeown, C.M.5
Neoptolemos, J.6
-
30
-
-
0030765423
-
The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutations
-
30 Reck AC, et al.: The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutations. Eye 1997, 11 (part 3):298-300.
-
(1997)
Eye
, vol.11
, Issue.PART 3
, pp. 298-300
-
-
Reck, A.C.1
-
31
-
-
0030202884
-
Exceptions to the rule: Individuals with FAP specific CHRPE and mutations in exon 6 of the APC gene
-
31 Pack K, Smith-Ravin J, Phillips RKS, Hodgson SV: Exceptions to the rule: individuals with FAP specific CHRPE and mutations in exon 6 of the APC gene. Clin Genet 1996, 50:110-111.
-
(1996)
Clin Genet
, vol.50
, pp. 110-111
-
-
Pack, K.1
Smith-Ravin, J.2
Phillips, R.K.S.3
Hodgson, S.V.4
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