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index medicus (31) 31
ophthalmology (28) 28
humans (25) 25
schnyder corneal dystrophy (21) 21
corneal dystrophy (18) 18
female (18) 18
cholesterol (17) 17
cornea (17) 17
male (17) 17
corneal dystrophies, hereditary - genetics (13) 13
middle aged (13) 13
schnyder crystalline corneal dystrophy (13) 13
adult (11) 11
corneal dystrophies, hereditary - pathology (10) 10
mutation (10) 10
ubiad1 (9) 9
gene (8) 8
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phototherapeutic keratectomy (8) 8
aged (7) 7
corneal dystrophies, hereditary - diagnosis (7) 7
crystalline dystrophy (7) 7
hyperlipoproteinemia (7) 7
visual acuity (7) 7
confocal microscopy (6) 6
cornea - pathology (6) 6
dystrophy (6) 6
family (6) 6
genetics & heredity (6) 6
mutations (6) 6
corneal dystrophies, hereditary - surgery (5) 5
corneal stroma - pathology (5) 5
crystals (5) 5
lattice corneal dystrophy (5) 5
lipid (5) 5
macular corneal dystrophy (5) 5
schnyder's corneal dystrophy (5) 5
thiel-behnke corneal dystrophy (5) 5
adolescent (4) 4
animals (4) 4
apolipoprotein-e (4) 4
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congenital hereditary endothelial dystrophy 1 (4) 4
congenital stromal corneal dystrophy (4) 4
corneal histopathology (4) 4
corneal opacity (4) 4
crystallization (4) 4
epithelial basement membrane dystrophy (4) 4
epithelial recurrent erosion dystrophy (4) 4
eponym (4) 4
excimer laser (4) 4
eye diseases (4) 4
fleck corneal dystrophy (4) 4
fuchs endothelial corneal dystrophy (4) 4
gelatinous drop-like corneal dystrophy (4) 4
gene mutations (4) 4
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granular corneal dystrophy 1 (4) 4
granular corneal dystrophy 2 (4) 4
grayson-wilbrandt corneal dystrophy (4) 4
hereditary endothelial dystrophy (4) 4
inherited corneal disease (4) 4
key reference (4) 4
lattice gelsolin type dystrophy (4) 4
lisch epithelial corneal dystrophy (4) 4
localization (4) 4
meesmann corneal dystrophy (4) 4
metabolism (4) 4
posterior amorphous corneal dystrophy (4) 4
posterior polymorphous corneal dystrophy (4) 4
pre-descemet corneal dystrophy (4) 4
prenyltransferase (4) 4
schnyder (4) 4
schnyder's crystalline dystrophy (4) 4
subepithelial mucinous corneal dystrophy (4) 4
ubiad1 gene (4) 4
carbohydrate sulfotransferase gene (3) 3
central cloudy dystrophy (3) 3
child, preschool (3) 3
chromosome 1p34.1-p36 (3) 3
compound heterozygous mutations (3) 3
congenital hereditary endothelial dystrophy 2 (3) 3
cornea - ultrastructure (3) 3
corneal dystrophies, hereditary - metabolism (3) 3
crystalline stromal dystrophy (3) 3
diagnosis, differential (3) 3
dna mutational analysis (3) 3
eye (3) 3
gelsolin-related amyloidosis (3) 3
genetic aspects (3) 3
genetic disease (3) 3
health aspects (3) 3
heredity (3) 3
hypercholesterolemia (3) 3
keratoplasty, penetrating (3) 3
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Experimental Eye Research, ISSN 0014-4835, 1983, Volume 36, Issue 2, pp. 279 - 286
Journal Article
Optometry and Vision Science, ISSN 1040-5488, 12/2013, Volume 90, Issue 12, pp. e301 - e304
PURPOSETo report a rare corneal dystrophy and its common findings to help aid others in proper and early diagnosis and management. CASE REPORTA 56-year-old... 
cholesterol | corneal dystrophy | crystals | Schnyder corneal dystrophy | arcus | lipid | PHOTOTHERAPEUTIC KERATECTOMY | OPHTHALMOLOGY | UBIAD1 GENE | MUTATIONS | Corneal Transplantation | Vision Disorders - diagnosis | Humans | Middle Aged | Corneal Dystrophies, Hereditary - surgery | Male | Cornea - pathology | Corneal Dystrophies, Hereditary - diagnosis | Index Medicus
Journal Article
Middle East African Journal of Ophthalmology, ISSN 0974-9233, 01/2011, Volume 18, Issue 1, pp. 61 - 64
Schnyder corneal dystrophy is a rare dominant disorder mostly reported in Western and occasionally Asian populations. This report documents the condition in an... 
Saudi Arabia | Schnyder Corneal Dystrophy | UBIAD1 | Cholesterol | Case studies | Care and treatment | Gene mutations | Patient outcomes | Corneal diseases | Diagnosis | Health aspects | Risk factors | Arabs | Eye diseases | Cornea | Mutation | Ophthalmology | Case Report
Journal Article
Journal Francais d'Ophtalmologie, ISSN 0181-5512, 04/2010, Volume 33, Issue 4, pp. 264 - e5
Schnyder's crystalline corneal dystrophy is a rare bilateral hereditary disease with various clinical features. It typically presents as a central disc-like... 
HRT II | Schnyder's corneal dystrophy | Anterior segment optical coherence tomography | In vivo confocal microscopy | Heredity
Journal Article
Journal Francais d'Ophtalmologie, ISSN 0181-5512, 2010, Volume 33, Issue 4, pp. 264.e1 - 264.e5
La dystrophie cristalline de Schnyder est une pathologie cornéenne héréditaire rare, dont les formes cliniques peuvent être variées. Elle se caractérise... 
HRT II | Tomographie en cohérence optique de segment antérieur | Schnyder's corneal dystrophy | Dystrophie cornéenne de Schnyder | Anterior segment optical coherence tomography | In vivo confocal microscopy | Hérédité | Microscopie confocale in vivo | Heredity
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 11/2018, Volume 256, Issue 11, pp. 2127 - 2134
Schnyder corneal dystrophy (SCD) is a rare inherited disease that leads to gradual vision loss by the deposition of lipids in the corneal stroma. The aim of... 
Pathogenic variant | UBIAD1 | Medicine & Public Health | Confocal microscopy | Ophthalmology | Schnyder corneal dystrophy | Optical coherent tomography | CHOLESTEROL | PHENOTYPE | FAMILY | METABOLISM | GENE | MUTATION | VITAMIN-K | OPHTHALMOLOGY | Medicine, Experimental | Medical research | Family | Lipids | Cornea | Corneal dystrophy | Stroma | Dystrophy | Localization | Age | Genetic screening | Index Medicus
Journal Article
대한안과학회지, ISSN 0378-6471, 1995, Volume 36, Issue 8, pp. 1363 - 1369
Journal Article
Romanian journal of ophthalmology, ISSN 2457-4325, 04/2018, Volume 62, Issue 2, pp. 175 - 180
to highlight the diagnostic and therapeutic challenges in a case with central and peripheral corneal lesions. We present the preoperative investigations:... 
Cornea - pathology | Corneal Dystrophies, Hereditary - diagnosis | Corneal Dystrophies, Hereditary - complications | Microscopy, Acoustic | Tomography, Optical Coherence | Humans | Index Medicus | Schnyder’s crystalline dystrophy | peripheral corneal degeneration | Case Reports
Journal Article
by Chae, H and Kim, M and Kim, Y and Kim, J and Kwon, A and Choi, H and Park, J and Jang, W and Lee, Y.S and Park, S.H and Kim, M.S
Clinical Genetics, ISSN 0009-9163, 06/2016, Volume 89, Issue 6, pp. 678 - 689
Corneal dystrophy typically refers to a group of rare hereditary disorders with a heterogeneous genetic background. A comprehensive molecular genetic analysis... 
posterior polymorphous corneal dystrophy | macular corneal dystrophy | molecular genetic analysis | Thiel–Behnke corneal dystrophy | Fuchs endothelial corneal dystrophy | granular corneal dystrophy | Schnyder corneal dystrophy | lattice corneal dystrophy | Korea | Molecular genetic analysis | Granular corneal dystrophy | Posterior polymorphous corneal dystrophy | Thiel-Behnke corneal dystrophy | Lattice corneal dystrophy | Macular corneal dystrophy | IC3D CLASSIFICATION | MISSENSE MUTATIONS | COL8A2 GENE | HEREDITARY ENDOTHELIAL DYSTROPHY | GENETICS & HEREDITY | BIGH3 GENE | L527R MUTATION | TGFBI GENE-MUTATIONS | JAPANESE PATIENTS | PROTEIN FUNCTION | LATTICE | Sulfotransferases - genetics | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Corneal Dystrophies, Hereditary - genetics | Family Health | Male | Corneal Dystrophies, Hereditary - ethnology | Zinc Finger E-box-Binding Homeobox 1 - genetics | Transforming Growth Factor beta - genetics | Dimethylallyltranstransferase - genetics | DNA Mutational Analysis | Pedigree | Base Sequence | Adult | Female | Genetic Predisposition to Disease - ethnology | Aged | Mutation | Republic of Korea | Collagen Type VIII - genetics | Genetic aspects | Gene mutations | Analysis | Endothelium | Eye diseases | Cornea | Genetic disorders | Index Medicus
Journal Article
OPHTHALMOLOGE, ISSN 0941-293X, 12/2012, Volume 109, Issue 12, pp. 1221 - 1223
A 17-year-old asymptomatic girl presented with discrete bilateral deposits in the superficial corneal stroma. The diagnosis of very early and in this form as... 
Schnyder's corneal dystrophy | Crystals | OPACITY | OPHTHALMOLOGY | Corneal deposits | Early manifestation | Crystalline keratopathy | Diagnosis, Differential | Corneal Dystrophies, Hereditary - pathology | Humans | Adolescent | Corneal Stroma - pathology | Female | Ophthalmoscopy - methods | Index Medicus
Journal Article
Der Ophthalmologe, ISSN 0941-293X, 12/2012, Volume 109, Issue 12, pp. 1221 - 1223
Ein 17-jähriges, asymptomatisches Mädchen stellte sich mit dezenten bilateralen Ablagerungen im oberflächlichen kornealen Stroma vor. Nur aufgrund der... 
Frühe Manifestation | Schnyder-Hornhautdystrophie | Medicine & Public Health | Korneale Ablagerungen | Crystals | Kristalle | Corneal deposits | Kristalline Keratopathien | Ophthalmology | Schnyder’s corneal dystrophy | Early manifestation | Crystalline keratopathy | Schnyder's corneal dystrophy
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 08/1997, Volume 211, Issue 2, pp. 135 - 137
Background Central crystalline dystrophy of Schnyder is characterized by the deposition of unesterified cholesterol crystals and lipids in the central and... 
low density lipoprotein | Schnyder's dystrophy | CHOLESTEROL | cornea | OPHTHALMOLOGY | CRYSTALLINE DYSTROPHY | hypercholesterolemia
Journal Article
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