X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (16) 16
index medicus (16) 16
male (14) 14
female (10) 10
mutation (8) 8
ophthalmology (8) 8
child (5) 5
genetic aspects (5) 5
genetics & heredity (5) 5
pedigree (5) 5
saudi arabia (5) 5
adolescent (4) 4
adult (4) 4
child, preschool (4) 4
consanguinity (3) 3
exome (3) 3
families (3) 3
gene mutations (3) 3
genetics (3) 3
heterozygote (3) 3
homozygote (3) 3
infant (3) 3
middle aged (3) 3
phenotype (3) 3
research (3) 3
aged (2) 2
analysis (2) 2
causes of (2) 2
cornea (2) 2
deafness (2) 2
diagnosis, differential (2) 2
dna mutational analysis (2) 2
eye diseases (2) 2
fatty acid metabolism (2) 2
flecked retina (2) 2
fluorescein angiography (2) 2
gene (2) 2
genes (2) 2
genes, recessive (2) 2
genetic predisposition to disease (2) 2
genotype (2) 2
hypotonia (2) 2
medical genetics (2) 2
otorhinolaryngology (2) 2
pediatrics (2) 2
peroxisomal disorders (2) 2
retina - pathology (2) 2
retinal dystrophies - genetics (2) 2
sense organs (2) 2
young adult (2) 2
zellweger-like phenotype (2) 2
3-hydroxyacyl coa dehydrogenases - deficiency (1) 1
age factors (1) 1
aged, 80 and over (1) 1
aicardi syndrome (1) 1
alpha-subunit (1) 1
alport syndrome (1) 1
amino acid sequence (1) 1
anemia - diagnosis (1) 1
angioendotheliomatosis proliferans systemisata (1) 1
animals (1) 1
aniridia (1) 1
aniridia - complications (1) 1
aniridia - genetics (1) 1
anophthalmia (1) 1
antibodies, monoclonal (1) 1
antinomy (1) 1
articles (1) 1
autoimmune diseases of the nervous system - complications (1) 1
autoimmune diseases of the nervous system - genetics (1) 1
autosomal-dominant (1) 1
autozygosity (1) 1
bacterial infections - microbiology (1) 1
bacterial keratitis (1) 1
base sequence (1) 1
basement-membrane nephropathy (1) 1
bile - metabolism (1) 1
biochemistry & molecular biology (1) 1
biotechnology & applied microbiology (1) 1
brain (1) 1
brain diseases, metabolic, inborn - genetics (1) 1
brain-tissue (1) 1
cadherins - genetics (1) 1
carboxypeptidases - genetics (1) 1
cataract - complications (1) 1
cataract extraction (1) 1
cells (1) 1
children (1) 1
choristoma - pathology (1) 1
choristoma - surgery (1) 1
chromosome mapping (1) 1
chromosomes, human, pair 3 - genetics (1) 1
chronic disease (1) 1
cicatrix - etiology (1) 1
ciliopathy (1) 1
clinical exome sequencing (1) 1
col4a3/col4a4 mutations (1) 1
col4a4 (1) 1
col4a5 collagen gene (1) 1
collagen (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


International Ophthalmology, ISSN 0165-5701, 03/1995, Volume 19, Issue 2, pp. 83 - 88
Kohl is a widely used traditional cosmetic. It is mainly worn around the eyes in the Middle East, Asia and Africa. The elemental composition of twenty-one kohl... 
toxicity | cosmetic | kohl | antinomy | EDAX | lead | COSMETIC | OPHTHALMOLOGY | TOXICITY | KOHL | ANTINOMY | SAUDI-ARABIA | LEAD | CHILDREN | Cosmetics - adverse effects | Lead - adverse effects | Saudi Arabia | Sulfides - analysis | Humans | Cosmetics - chemistry | Eyelids | Sulfides - adverse effects | Lead - analysis | Infant | Lead Poisoning - etiology | Index Medicus
Journal Article
Ophthalmology, ISSN 0161-6420, 11/1988, Volume 95, Issue 11, pp. 1504 - 1508
Journal Article
Ophthalmology, ISSN 0161-6420, 06/1993, Volume 100, Issue 6, pp. 961 - 965
Angiotropic large cell lymphoma is a rare, generally fatal disease characterized by multifocal proliferation of neoplastic mononuclear cells within the lumens... 
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 1999, Volume 20, Issue 1, pp. 45 - 51
Background: Optic disc elevation associated with Down syndrome is an uncommon phenomenon and raises the suspicion of an intracranial space-occupying lesion,... 
Intracranial Pressure | Down Syndrome - pathology | Humans | Child, Preschool | Female | Male | Child | Fundus Oculi | Optic Disk - pathology | Fluorescein Angiography | Index Medicus
Journal Article
Ophthalmic Genetics, ISSN 0167-6784, 1999, Volume 20, Issue 1, pp. 45 - 51
Journal Article
Ophthalmic Genetics, ISSN 0167-6784, 06/1997, Volume 18, Issue 2, pp. 93 - 99
Peroxisomal disorders include single enzyme defects and defects of peroxisomal fatty acid oxidation enzymes. Peroxisomal bifunctional enzyme complex deficiency... 
Hyptonia | Fatty acid metabolism | Flecked retina | Zellweger-like phenotype | Peroxisomal disorders | peroxisomal disorders | fatty acid metabolism | GENETICS & HEREDITY | DISORDER | OPHTHALMOLOGY | NEONATAL ADRENOLEUKODYSTROPHY | flecked retina | hypotonia | ZELLWEGER
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 12/1993, Volume 77, Issue 12, pp. 817 - 818
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.