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index medicus (179) 179
humans (174) 174
ophthalmology (146) 146
male (124) 124
female (110) 110
corneal dystrophies, hereditary - genetics (93) 93
middle aged (91) 91
adult (82) 82
mutation (82) 82
lattice corneal dystrophy (78) 78
aged (67) 67
transforming growth factor beta - genetics (65) 65
lattice (64) 64
corneal dystrophies, hereditary - pathology (59) 59
extracellular matrix proteins - genetics (58) 58
pedigree (56) 56
dna mutational analysis (49) 49
protein (41) 41
bigh3 gene (40) 40
amyloidosis (38) 38
corneal dystrophy (37) 37
beta-ig-h3 (35) 35
corneal dystrophies, hereditary - surgery (35) 35
lattice corneal-dystrophy (34) 34
cornea (33) 33
phenotype (33) 33
gene (30) 30
corneal dystrophies, hereditary - metabolism (29) 29
biochemistry & molecular biology (28) 28
point mutation (28) 28
gelsolin (27) 27
polymerase chain reaction (27) 27
cornea - pathology (26) 26
kerato-epithelin mutations (25) 25
lattice dystrophy (25) 25
tgfbi (25) 25
adolescent (23) 23
amyloidosis - genetics (23) 23
corneal dystrophies, hereditary - diagnosis (23) 23
keratoplasty, penetrating (23) 23
granular corneal dystrophy (22) 22
growth-factor-beta (22) 22
mutations (22) 22
aged, 80 and over (21) 21
amyloid - metabolism (21) 21
cranial neuropathy (21) 21
eye diseases (21) 21
molecular sequence data (21) 21
base sequence (20) 20
recurrence (20) 20
corneal lattice dystrophy (19) 19
penetrating keratoplasty (19) 19
tgfbi gene (19) 19
bigh3 (18) 18
child (18) 18
familial amyloidosis (18) 18
phototherapeutic keratectomy (18) 18
retrospective studies (17) 17
gelsolin - genetics (16) 16
mutation, missense (16) 16
corneal stroma - pathology (15) 15
deposits (15) 15
genetic aspects (15) 15
hereditary amyloidosis (15) 15
visual acuity (15) 15
amyloid (14) 14
corneal dystrophies, hereditary - complications (14) 14
dystrophy (14) 14
genetics & heredity (14) 14
genotype (14) 14
mutation - genetics (14) 14
avellino corneal dystrophy (13) 13
corneal dystrophies, hereditary - physiopathology (13) 13
genetics (13) 13
amyloidosis - pathology (12) 12
avellino (12) 12
child, preschool (12) 12
cornea - metabolism (12) 12
follow-up studies (12) 12
genes (12) 12
granular dystrophy (12) 12
kerato-epithelin (12) 12
analysis (11) 11
corneal dystrophies, hereditary - classification (11) 11
exons (11) 11
exons - genetics (11) 11
medicine & public health (11) 11
reis-bucklers (11) 11
amino acid sequence (10) 10
amyloid deposits (10) 10
asian continental ancestry group - genetics (10) 10
clinical neurology (10) 10
epithelium (10) 10
finland (10) 10
finnish type (10) 10
immunohistochemistry (10) 10
keratoepithelin (10) 10
keratoplasty (10) 10
microscopy, confocal (10) 10
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Ophthalmic Research, ISSN 0030-3747, 1975, Volume 7, Issue 3, pp. 194 - 203
Pseudoexfoliation (PE) syndrome in addition to inherited systemic amyloidosis with lattice corneal dystrophy is reported in 1 clinical case, and in 5 cases out... 
Paper | Corneal lattice dystrophy | Glaucoma | Amyloidosis | Pseudoexfoliation
Journal Article
Ophthalmology, ISSN 0161-6420, 1981, Volume 88, Issue 12, pp. 1239 - 1243
The corneal button of a patient with lattice corneal dystrophy and the clinical features of elastotic degeneration was subjected to histochemical and electron... 
autofluorescence | elastotic degeneration | lattice corneal dystrophy | elastosis | OPHTHALMOLOGY | Cornea - metabolism | Elastin - metabolism | Corneal Dystrophies, Hereditary - pathology | Humans | Middle Aged | Staining and Labeling | Histocytochemistry | Fluorescence | Male | Cornea - pathology | Corneal Dystrophies, Hereditary - metabolism | Index Medicus
Journal Article
Ophthalmology, ISSN 0161-6420, 12/1981, Volume 88, Issue 12, pp. 1239 - 1243
The corneal button of a patient with lattice corneal dystrophy and the clinical features of elastotic degeneration was subjected to histochemical and electron... 
autofluorescence | elastotic degeneration | lattice corneal dystrophy | elastosis
Journal Article
Ophthalmology, ISSN 0161-6420, 12/1983, Volume 90, Issue 12, pp. 1512 - 1517
Journal Article
Experimental Eye Research, ISSN 0014-4835, 1983, Volume 36, Issue 2, pp. 181 - 186
We examined the amyloid deposits of lattice dystrophy type I for common components of primary and secondary amyloid using the sensitive unlabelled antibody... 
lattice dystrophy | amyloid P protein | cornea | amyloid A protein | Humans | Serum Amyloid P-Component | Corneal Dystrophies, Hereditary - metabolism | Amyloid - analysis | Immunoenzyme Techniques | Serum Amyloid A Protein - analysis | Cornea - analysis | Index Medicus
Journal Article
International Ophthalmology, ISSN 0165-5701, 1987, Volume 10, Issue 1, pp. 47 - 53
A Japanese family with 4 members suffering from lattice dystrophy of the cornea is reported. Their central corneas were affected leaving the peripheral zone... 
branching lines | specular microscopy | crateriform lesions | lattice corneal dystrophy | Corneal Dystrophies, Hereditary - pathology | Pedigree | Humans | Middle Aged | Corneal Dystrophies, Hereditary - genetics | Adult | Female | Aged | Cornea - pathology | Child | Amyloid - analysis | Index Medicus
Journal Article
Journal Article
Ophthalmology, ISSN 0161-6420, 01/1988, Volume 95, Issue 1, pp. 46 - 51
Four patients from families in Pennsylvania, Massachusetts, and Argentina were diagnosed clinically as having granular dystrophy. Results of pathologic... 
granular | amyloid | dystrophy | cornea | lattice
Journal Article
Ophthalmology, ISSN 0161-6420, 1988, Volume 95, Issue 1, pp. 46 - 51
Four patients from families in Pennsylvania, Massachusetts, and Argentina were diagnosed clinically as having granular dystrophy. Results of pathologic... 
amyloid | cornea | lattice | granular | dystrophy
Journal Article
Acta Ophthalmologica, ISSN 0001-639X, 1989, Volume 67, Issue 192 S, pp. 171 - 173
Journal Article
Cornea, ISSN 0277-3740, 1991, Volume 10, Issue 1, pp. 13 - 16
Journal Article
Journal Article
ACTA OPHTHALMOLOGICA, ISSN 1755-375X, 1991, Volume 69, pp. U1 - U1
Journal Article
JOURNAL FRANCAIS D OPHTALMOLOGIE, ISSN 0181-5512, 1992, Volume 15, Issue 11, pp. 592 - 595
The authors conducted a study in a family pedigree comprising 33 patients (men 16, women 17). In this pedigree there coexisted patients with progressive... 
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA | AUTOSOMAL DOMINANT | OPHTHALMOLOGY | LATTICE CORNEAL DYSTROPHY
Journal Article
Cornea, ISSN 0277-3740, 07/1992, Volume 11, Issue 4, pp. 343 - 350
Journal Article
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