-
1
-
-
0001001932
-
A rare case of corneal dystrophy
-
Nakaizumi K. A rare case of corneal dystrophy. Acta Soc Ophthalmol Jpn. 1914; 18:949-950.
-
(1914)
Acta Soc Ophthalmol Jpn.
, vol.18
, pp. 949-950
-
-
Nakaizumi, K.1
-
2
-
-
0025687619
-
Histopathologic and immunohistochemical findings in gelatinous drop-like corneal dystrophy
-
Akiya S, Furukawa H, Sakamoto H, Takahashi H, Sakka Y. Histopathologic and immunohistochemical findings in gelatinous drop-like corneal dystrophy. Ophthalmic Res. 1990;22:371-376.
-
(1990)
Ophthalmic Res.
, vol.22
, pp. 371-376
-
-
Akiya, S.1
Furukawa, H.2
Sakamoto, H.3
Takahashi, H.4
Sakka, Y.5
-
3
-
-
0005960147
-
Gelatinous drop-like dystrophy of the cornea: Light and electron microscopy study of superficial stromal lesion
-
Akiya S, Ito K, Matsui M. Gelatinous drop-like dystrophy of the cornea: light and electron microscopy study of superficial stromal lesion. Jpn J Clin Ophthalmol. 1972;26:815-826.
-
(1972)
Jpn J Clin Ophthalmol.
, vol.26
, pp. 815-826
-
-
Akiya, S.1
Ito, K.2
Matsui, M.3
-
4
-
-
0026325298
-
Inherited corneal amyloidosis predominantly manifested in one eye
-
Akiya S, Nagaya K, Fukui A, Hamada T, Takahashi H, Furukawa H. Inherited corneal amyloidosis predominantly manifested in one eye. Ophthalmologica. 1991; 203:204-207.
-
(1991)
Ophthalmologica
, vol.203
, pp. 204-207
-
-
Akiya, S.1
Nagaya, K.2
Fukui, A.3
Hamada, T.4
Takahashi, H.5
Furukawa, H.6
-
5
-
-
15644378644
-
Histochemical and electron microscopic examinations and so-called 'gelatinous drop-like dystrophy of the cornea'
-
Matsui M, Ito K, Akiya S. Histochemical and electron microscopic examinations and so-called 'gelatinous drop-like dystrophy of the cornea.' Folia Ophthalmol Jap. 1967;18:436-447.
-
(1967)
Folia Ophthalmol Jap.
, vol.18
, pp. 436-447
-
-
Matsui, M.1
Ito, K.2
Akiya, S.3
-
6
-
-
0000709387
-
A case of primary gelatinous drop-like corneal dystrophy
-
Nagataki S, Tanishima T, Sakimoto T. A case of primary gelatinous drop-like corneal dystrophy. Jpn J Ophthalmol. 1972;16:107-116.
-
(1972)
Jpn J Ophthalmol.
, vol.16
, pp. 107-116
-
-
Nagataki, S.1
Tanishima, T.2
Sakimoto, T.3
-
8
-
-
0028795757
-
Long-term follow-up of patients with familial subepielial amyloidosis of the cornea
-
Shimazaki J, Hida T, Inoue M, Saito H, Tsubota K. Long-term follow-up of patients with familial subepielial amyloidosis of the cornea. Ophthalmology. 1995;102:139-144.
-
(1995)
Ophthalmology
, vol.102
, pp. 139-144
-
-
Shimazaki, J.1
Hida, T.2
Inoue, M.3
Saito, H.4
Tsubota, K.5
-
9
-
-
0022002262
-
Unusual inclusions in stromal macrophages in a case of gelatinous drop-like corneal dystrophy
-
Takahashi M, Yokota T, Yamashita Y, et al. Unusual inclusions in stromal macrophages in a case of gelatinous drop-like corneal dystrophy. Am J Ophthalmol. 1985;99:312-316.
-
(1985)
Am J Ophthalmol.
, vol.99
, pp. 312-316
-
-
Takahashi, M.1
Yokota, T.2
Yamashita, Y.3
-
10
-
-
15644383045
-
Gelatinous drop-like corneal dystrophy: Case report with histopathological findings
-
Shindo S. Gelatinous drop-like corneal dystrophy: Case report with histopathological findings. Jpn J Clin Ophthalmol. 1969;23:1167-1174.
-
(1969)
Jpn J Clin Ophthalmol.
, vol.23
, pp. 1167-1174
-
-
Shindo, S.1
-
11
-
-
0029952397
-
Clinicohistopathological findings of gelatinous droplike corneal dystrophy among Asians
-
Li S, Edward DP, Ratnakar KS, Reddy M, Tso MOM. Clinicohistopathological findings of gelatinous droplike corneal dystrophy among Asians. Cornea. 1996; 15:355-362.
-
(1996)
Cornea
, vol.15
, pp. 355-362
-
-
Li, S.1
Edward, D.P.2
Ratnakar, K.S.3
Reddy, M.4
Tso, M.O.M.5
-
12
-
-
0025728747
-
Forme familiale de dystrophie gélatineuse en gouttes de la cornée
-
el Matri L, Bachtobji A, Ghorbal M, et al. Forme familiale de dystrophie gélatineuse en gouttes de la cornée. J Fr Ophtalmol. 1991;14:125-129.
-
(1991)
J Fr Ophtalmol.
, vol.14
, pp. 125-129
-
-
El Matri, L.1
Bachtobji, A.2
Ghorbal, M.3
-
13
-
-
0018904839
-
Gelatinous drop-like dystrophy: A form of primary corneal amyloidosis
-
Weber FL, Babel J. Gelatinous drop-like dystrophy: A form of primary corneal amyloidosis. Arch Ophthalmol. 1980;98:144-148.
-
(1980)
Arch Ophthalmol.
, vol.98
, pp. 144-148
-
-
Weber, F.L.1
Babel, J.2
-
16
-
-
0015318852
-
Localized corneal amyloidosis: Case report with electron microscopic observations
-
Ramsey MS, Fine BS, Cohen SW. Localized corneal amyloidosis: Case report with electron microscopic observations. Am J Ophthalmol. 1972;73:560-565.
-
(1972)
Am J Ophthalmol.
, vol.73
, pp. 560-565
-
-
Ramsey, M.S.1
Fine, B.S.2
Cohen, S.W.3
-
17
-
-
0017164337
-
Primary familial amyloidosis of the cornea
-
Stock EL, Kielar RA. Primary familial amyloidosis of the cornea. Am J Ophthalmol. 1976;82:266-271.
-
(1976)
Am J Ophthalmol.
, vol.82
, pp. 266-271
-
-
Stock, E.L.1
Kielar, R.A.2
-
20
-
-
0008531395
-
Ueber einen Fall primärer Degenerationamyloidose der Kornea
-
Lewkojewa EF. Ueber einen Fall primärer Degenerationamyloidose der Kornea. Klin Mbl Augenheilk. 1930; 85:117-137.
-
(1930)
Klin Mbl Augenheilk
, vol.85
, pp. 117-137
-
-
Lewkojewa, E.F.1
-
21
-
-
0007960924
-
A case of familial corneal dystrophy
-
Kiyosawa M. A case of familial corneal dystrophy. Nippon Ganka Gakkai Zasshi. 1932;36:1634-1635.
-
(1932)
Nippon Ganka Gakkai Zasshi
, vol.36
, pp. 1634-1635
-
-
Kiyosawa, M.1
-
22
-
-
0019826715
-
Primary familial amyloidosis of the cornea
-
Mondino BJ, Rabb MF, SugarJ, Sundar Raj CV, Brown SI. Primary familial amyloidosis of the cornea. Am J Ophthalmol. 1981;92:732-736.
-
(1981)
Am J Ophthalmol.
, vol.92
, pp. 732-736
-
-
Mondino, B.J.1
Rabb, M.F.2
Sugar, J.3
Sundar Raj, C.V.4
Brown, S.I.5
-
23
-
-
0024205666
-
Light and electron microscopic study of gelatinous drop-like corneal dystrophy with deeper stromal involvement
-
Fujita S, Sameshima M, Hirashima S, Nakao K. Light and electron microscopic study of gelatinous drop-like corneal dystrophy with deeper stromal involvement. Acta Soc Ophthalmol (Jpn). 1988;92:1744-1757.
-
(1988)
Acta Soc Ophthalmol (Jpn)
, vol.92
, pp. 1744-1757
-
-
Fujita, S.1
Sameshima, M.2
Hirashima, S.3
Nakao, K.4
-
24
-
-
0020692184
-
Amyloidogenesis in organ-limited cutaneous amyloidosis: An antigenic identity between epidermal keratin and skin amyloid
-
Kobayashi H, Hashimoto K. Amyloidogenesis in organ-limited cutaneous amyloidosis: An antigenic identity between epidermal keratin and skin amyloid. J Invest Dennatol. 1983;80:66-72.
-
(1983)
J Invest Dennatol.
, vol.80
, pp. 66-72
-
-
Kobayashi, H.1
Hashimoto, K.2
-
25
-
-
0018852604
-
Studies on cutaneous amyloidosis with antikeratin antibody
-
Masu S, Hosokawa M, Seiji M. Studies on cutaneous amyloidosis with antikeratin antibody. Nippon Hifuka Gakkai Zasshi. 1980;90:623-626.
-
(1980)
Nippon Hifuka Gakkai Zasshi
, vol.90
, pp. 623-626
-
-
Masu, S.1
Hosokawa, M.2
Seiji, M.3
-
26
-
-
0019792891
-
Analysis of protein and peptide mixtures: Evaluation of three sodium dodecyl sulphate-polyacrylamide gel electrophoresis buffer systems
-
Bury AF. Analysis of protein and peptide mixtures: Evaluation of three sodium dodecyl sulphate-polyacrylamide gel electrophoresis buffer systems. J Chromatogr. 1981;213:491-500.
-
(1981)
J Chromatogr.
, vol.213
, pp. 491-500
-
-
Bury, A.F.1
-
27
-
-
0009482260
-
Electrophoretic transfer of proteins from polyacrylamide gels to nitro-cellulose sheets: Procedure and some applications
-
Towbin H, Staehelin T, Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitro-cellulose sheets: Procedure and some applications. Proc Natl Acad Sci USA. 1979;76:4350-4354.
-
(1979)
Proc Natl Acad Sci USA
, vol.76
, pp. 4350-4354
-
-
Towbin, H.1
Staehelin, T.2
Gordon, J.3
-
28
-
-
0023664635
-
Sequence from picomole quantities of proteins electroblotted onto polyvinylidene difluoride membranes
-
Matsudaira P. Sequence from picomole quantities of proteins electroblotted onto polyvinylidene difluoride membranes. J Biol Chem. 1987;62:10035-10038.
-
(1987)
J Biol Chem.
, vol.62
, pp. 10035-10038
-
-
Matsudaira, P.1
-
29
-
-
0019423594
-
Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: A comparison between ABC and unlabeled antibody (PAP) procedures
-
Hsu SM, Raine L, Fanger H. Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: A comparison between ABC and unlabeled antibody (PAP) procedures. J Histochem Cytochem. 1981;29:577-580.
-
(1981)
J Histochem Cytochem.
, vol.29
, pp. 577-580
-
-
Hsu, S.M.1
Raine, L.2
Fanger, H.3
-
30
-
-
0024587683
-
Lactotransferrin gene expression in the mouse uterus and mammary gland
-
Teng CT, Pentecost BT, Chen YH, Newbold RR, Eddy EM, McLachlan JA. Lactotransferrin gene expression in the mouse uterus and mammary gland. Endocrinology. 1989;124:992-999.
-
(1989)
Endocrinology
, vol.124
, pp. 992-999
-
-
Teng, C.T.1
Pentecost, B.T.2
Chen, Y.H.3
Newbold, R.R.4
Eddy, E.M.5
McLachlan, J.A.6
-
32
-
-
0009665799
-
An iron-binding protein common to many external secretions
-
Masson PL, Heremans JF, Dive C. An iron-binding protein common to many external secretions. Clin Chim Acta. 1966;14:735-739.
-
(1966)
Clin Chim Acta
, vol.14
, pp. 735-739
-
-
Masson, P.L.1
Heremans, J.F.2
Dive, C.3
-
33
-
-
0014574791
-
Lactoferrin, an iron-binding protein in neutrophilic leukocytes
-
Masson PL, Heremans JF, Schonne E. Lactoferrin, an iron-binding protein in neutrophilic leukocytes. J Exp Med. 1969;130:643-658.
-
(1969)
J Exp Med.
, vol.130
, pp. 643-658
-
-
Masson, P.L.1
Heremans, J.F.2
Schonne, E.3
-
34
-
-
0021677758
-
Human lactotransferrin: Amino acid sequence and structural comparisons with other transferrins
-
Metz-Boutigue M-H, Jolles J, Mazuricr J, et al. Human lactotransferrin: Amino acid sequence and structural comparisons with other transferrins. Eur J Biochem. 1984;145:659-676.
-
(1984)
Eur J Biochem.
, vol.145
, pp. 659-676
-
-
Metz-Boutigue, M.-H.1
Jolles, J.2
Mazuricr, J.3
-
35
-
-
0023664683
-
Lactotransferrin is the major estrogen inducible protein of mouse uterine secretions
-
Pentecost BT, Teng CT. Lactotransferrin is the major estrogen inducible protein of mouse uterine secretions. J Biol Chem. 1987;262:10134-10139.
-
(1987)
J Biol Chem.
, vol.262
, pp. 10134-10139
-
-
Pentecost, B.T.1
Teng, C.T.2
-
36
-
-
0024389662
-
Structure of human lactoferrin: Crystallographic structure analysis and refinement at 2.8 A resolution
-
Anderson BF, Baker HM, Norris GE, Rice DW, Baker EN. Structure of human lactoferrin: Crystallographic structure analysis and refinement at 2.8 A resolution. J Mol Biol. 1989;209:711-734.
-
(1989)
J Mol Biol.
, vol.209
, pp. 711-734
-
-
Anderson, B.F.1
Baker, H.M.2
Norris, G.E.3
Rice, D.W.4
Baker, E.N.5
-
37
-
-
0025866839
-
Polymorphism and altered methylation of the lactoferrin gene in normal leukocytes, leukemic cells, and breast cancer
-
Panella TJ, Liu Y, Huang AT, Teng CT. Polymorphism and altered methylation of the lactoferrin gene in normal leukocytes, leukemic cells, and breast cancer. Cancer Res. 1991;51:3037-3043.
-
(1991)
Cancer Res.
, vol.51
, pp. 3037-3043
-
-
Panella, T.J.1
Liu, Y.2
Huang, A.T.3
Teng, C.T.4
-
38
-
-
0008144817
-
Primary structure of the human melanoma-associated antigen p97 (melanotransferrin) deduced from the mRNA sequence
-
Rose TM, Plowman GD, Teplow DB, Dreyer WJ, Hellstrom KE, Brown JP. Primary structure of the human melanoma-associated antigen p97 (melanotransferrin) deduced from the mRNA sequence. Proc Natl Acad Sci USA. 1986;83:1261-1265.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 1261-1265
-
-
Rose, T.M.1
Plowman, G.D.2
Teplow, D.B.3
Dreyer, W.J.4
Hellstrom, K.E.5
Brown, J.P.6
-
39
-
-
0000242640
-
The evolution of transferrin
-
Williams J. The evolution of transferrin. Trends Biochem Sci. 1982;7:394-397.
-
(1982)
Trends Biochem Sci.
, vol.7
, pp. 394-397
-
-
Williams, J.1
-
40
-
-
0023922603
-
Chromosomal localization of human lactotransferrin gene (LTF) by in situ hybridization
-
McCombs JL, Teng CT, Pentecost BT, Mangnuson VL, Moore CM, McGill JR. Chromosomal localization of human lactotransferrin gene (LTF) by in situ hybridization. Cytogenet Cell Genet. 1988;47:16-17.
-
(1988)
Cytogenet Cell Genet.
, vol.47
, pp. 16-17
-
-
McCombs, J.L.1
Teng, C.T.2
Pentecost, B.T.3
Mangnuson, V.L.4
Moore, C.M.5
McGill, J.R.6
-
41
-
-
0023448965
-
Assignment of the lactotransferrin gene to human chromosome 3 and to mouse chromosome 9
-
Teng CT, Pentecost BT, Marshall T, et al. Assignment of the lactotransferrin gene to human chromosome 3 and to mouse chromosome 9. Somatic Cell Mole Genet. 1987;13:689-693.
-
(1987)
Somatic Cell Mole Genet.
, vol.13
, pp. 689-693
-
-
Teng, C.T.1
Pentecost, B.T.2
Marshall, T.3
-
45
-
-
0027958193
-
Dystrophie gélatineuse de la cornée. A propos de 5 observations
-
Lasram L, Rais C, el Euch M, Ouertani A. Dystrophie gélatineuse de la cornée. A propos de 5 observations. J Fr Ophtalmol. 1994;17:24-28.
-
(1994)
J Fr Ophtalmol.
, vol.17
, pp. 24-28
-
-
Lasram, L.1
Rais, C.2
El Euch, M.3
Ouertani, A.4
-
46
-
-
0028345097
-
Primary gelatinous drop-like corneal dystrophy in a white woman. A pathologic, ultrastructural, and immunohistochemical study
-
Büchi ER, Daicker B, Uffer S, Gudat F. Primary gelatinous drop-like corneal dystrophy in a white woman. A pathologic, ultrastructural, and immunohistochemical study. Cornea. 1994;13:190-194.
-
(1994)
Cornea
, vol.13
, pp. 190-194
-
-
Büchi, E.R.1
Daicker, B.2
Uffer, S.3
Gudat, F.4
-
47
-
-
0026936594
-
Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187
-
de la Chapelle A, Tolvanen R, Boysen G, et al. Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187. Nature Genet. 1992;2:157-160.
-
(1992)
Nature Genet.
, vol.2
, pp. 157-160
-
-
De La Chapelle, A.1
Tolvanen, R.2
Boysen, G.3
-
48
-
-
0026410035
-
Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II
-
Gorevic PD, Munoz PC, Gorgone G, et al. Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II [see comments]. N Engl J Med. 1991;325:1780-1785.
-
(1991)
N Engl J Med.
, vol.325
, pp. 1780-1785
-
-
Gorevic, P.D.1
Munoz, P.C.2
Gorgone, G.3
-
49
-
-
0025936659
-
Finnish type of familial amyloidosis: Cosegregation of Asp187-Asn mutation of gelsolin with the disease in three large families
-
Hiltunen T, Kiuru S, Hongell V, Helio T, Paio J, Peltonen L. Finnish type of familial amyloidosis: Cosegregation of Asp187-Asn mutation of gelsolin with the disease in three large families [see comments]. Am J Hum Genet. 1991;49:522-528.
-
(1991)
Am J Hum Genet.
, vol.49
, pp. 522-528
-
-
Hiltunen, T.1
Kiuru, S.2
Hongell, V.3
Helio, T.4
Paio, J.5
Peltonen, L.6
-
50
-
-
15644370164
-
Familial gelsolin amyloidosis, Danish subtype (Tyr-187): Immunohistochemical localization of amyloid with antigelsolin (P 231-242) antibodies
-
Kisivsky R, Benson MD, Frangione B, Gaudie J, Muckle TJ, Young ID, eds. New York: Parthenon Publishing
-
Maury CPJ, Tornroth T, Boysen G, de la Chapelle A, Rossi H. Familial gelsolin amyloidosis, Danish subtype (Tyr-187): Immunohistochemical localization of amyloid with antigelsolin (P 231-242) antibodies. In: Kisivsky R, Benson MD, Frangione B, Gaudie J, Muckle TJ, Young ID, eds. Amyloid and Amyloidosis 1993. New York: Parthenon Publishing; 1994:617-619.
-
(1994)
Amyloid and Amyloidosis 1993
, pp. 617-619
-
-
Maury, C.P.J.1
Tornroth, T.2
Boysen, G.3
De La Chapelle, A.4
Rossi, H.5
-
51
-
-
0029063417
-
Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan
-
Paunio T, Sunada Y, Kiuru S, et al. Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan. 1995; Hum Mutat. 6:60-65.
-
(1995)
Hum Mutat.
, vol.6
, pp. 60-65
-
-
Paunio, T.1
Sunada, Y.2
Kiuru, S.3
-
52
-
-
0027087187
-
Familial amyloidosis
-
Benson MD. Familial amyloidosis. J Intern Med. 1992;232:525-527.
-
(1992)
J Intern Med.
, vol.232
, pp. 525-527
-
-
Benson, M.D.1
-
53
-
-
0026333630
-
Familial nephropathic non-neuropathic amyloidosis: Clinical features, immunohistochemistry and chemistry
-
Zalin AM, Jones S, Fitch NJ, Ramsden DB. Familial nephropathic non-neuropathic amyloidosis: Clinical features, immunohistochemistry and chemistry. Q J Med. 1991;81:945-956.
-
(1991)
Q J Med.
, vol.81
, pp. 945-956
-
-
Zalin, A.M.1
Jones, S.2
Fitch, N.J.3
Ramsden, D.B.4
-
54
-
-
0024504130
-
Selective defect in myeloid cell lactoferrin gene expression in neutrophil specific granule deficiency
-
Lomax KJ, Gallin JI, Rotrosen D, et al. Selective defect in myeloid cell lactoferrin gene expression in neutrophil specific granule deficiency. J Clin Invest. 1989; 83:514-519.
-
(1989)
J Clin Invest.
, vol.83
, pp. 514-519
-
-
Lomax, K.J.1
Gallin, J.I.2
Rotrosen, D.3
-
55
-
-
0028223723
-
Three autosomal dominant corneal dystrophies map to chromosome 5q
-
Stone EM, Mathers WD, Rosenwasser GO, et al. Three autosomal dominant corneal dystrophies map to chromosome 5q. Nature Genet. 1994;6:47-51.
-
(1994)
Nature Genet.
, vol.6
, pp. 47-51
-
-
Stone, E.M.1
Mathers, W.D.2
Rosenwasser, G.O.3
-
56
-
-
0028954349
-
Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval
-
Gregory CY, Evans K, Bhattacharya SS. Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval. J Med Genet. 1995;32:224-226.
-
(1995)
J Med Genet.
, vol.32
, pp. 224-226
-
-
Gregory, C.Y.1
Evans, K.2
Bhattacharya, S.S.3
-
57
-
-
0031020733
-
Kerato-epithelin mutations in four 5q31-linked corneal dystrophies
-
Munier FL, Korvatska E, Djemai A, et al. Kerato-epithelin mutations in four 5q31-linked corneal dystrophies. Nature Genetics. 1997;15:247-251.
-
(1997)
Nature Genetics
, vol.15
, pp. 247-251
-
-
Munier, F.L.1
Korvatska, E.2
Djemai, A.3
|