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American Journal of Ophthalmology, ISSN 0002-9394, 11/2018, Volume 195, pp. xv - xvii
A 2010 New England Journal of Medicine (NEJM) case report entitled “Schnyder Crystalline Corneal Dystrophy” incorrectly reported that affected patients should... 
OPHTHALMOLOGY | IC3D CLASSIFICATION | Medical personnel | 21st century | Pathology | Genotype & phenotype | Pediatrics | Histopathology | Publications | Ophthalmology | Mutation
Journal Article
Neuropediatrics, 06/2017, Volume 48, Issue 3, p. 185
Tadpole pupil is a rarely encountered phenomenon caused by episodic, segmental iris dilator muscle spasm of short duration (2-15 minutes), occurring in... 
Diagnosis, Differential | Pupil - physiology | Pupil Disorders - diagnosis | Pupil Disorders - etiology | Humans | Pupil Disorders - physiopathology | Adolescent | Arthritis, Juvenile - complications | Female | Exercise - physiology | Arthritis, Juvenile - drug therapy
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 09/2012, Volume 96, Issue 9, p. 1227
Journal Article
Ugeskrift for Laeger, ISSN 0041-5782, 03/2013, Volume 175, Issue 10, p. 661
Journal Article
Cornea, ISSN 0277-3740, 02/2015, Volume 34, Issue 2, pp. 117 - 159
PURPOSE:To update the 2008 International Classification of Corneal Dystrophies (IC3D) incorporating new clinical, histopathologic, and genetic information.... 
Fleck corneal dystrophy | Cornea | Epithelial and subepithelial dystrophies | Descemetmembrane | Posterior amorphous corneal dystrophy | Confocal microscopy | Cornea pathology | Thiel-Behnke corneal dystrophy | Lattice corneal dystrophy | Macular corneal dystrophy | Stromal dystrophies | Hereditary disease | Epithelial basement membranedystrophy | Pre-Descemet corneal dystrophy | Histopathology | Keratoconus | Congenital corneal endothelial dystrophy and X-linked endothelialdystrophy | Bowman membrane | Subepithelialmucinous corneal dystrophy | Endothelial dystrophies | Genetics | Schnyder corneal dystrophy | Gelatinousdrop-like corneal dystrophy | Fuchsendothelial corneal dystrophy | Epithelial-stromal TGFBI dystrophies | Lisch epithelial corneal dystrophy | Stroma | Histology | Meesmann dystrophy | Epithelium | Endothelium | Genetic disease | Epithelial recurrent erosion dystrophies | Posteror polymorphous corneal dystrophy | Centralcloudy dystrophy of François | Granular corneal dystrophy type 1 | Granular corneal dystrophy type 2 | TGFBI | Reis-Bücklers corneal dystrophy | Congenital stromal corneal dystrophy | Cornea dystrophy | cornea | endothelial dystrophies | histology | epithelial basement membrane dystrophy | genetic disease | epithelial and subepithelial dystrophies | central cloudy dystrophy of Francois | macular corneal dystrophy | subepithelial mucinous corneal dystrophy | cornea pathology | stroma | FRANCOIS | congenital corneal endothelial dystrophy and X-linked endothelial dystrophy | posteror polymorphous corneal dystrophy | DISEASE | epithelium | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy | pre-Descemet corneal dystrophy | histopathology | INDIVIDUAL PHENOTYPIC VARIANCES | FAMILY | epithelial recurrent erosion dystrophies | granular corneal dystrophy type 1 | granular corneal dystrophy type 2 | genetics | cornea dystrophy | UBIAD1 GENE | MUTATIONS | Descemet membrane | endothelium | hereditary disease | epithelial-stromal TGFBI dystrophies | keratoconus | posterior amorphous corneal dystrophy | congenital stromal corneal dystrophy | stromal dystrophies | fleck corneal dystrophy | confocal microscopy | gelatinous drop-like corneal dystrophy | EDEMA | OPHTHALMOLOGY | LINKAGE | Corneal Dystrophies, Hereditary - genetics | Terminology as Topic | International Classification of Diseases | Corneal Dystrophies, Hereditary - classification | Corneal Dystrophies, Hereditary - pathology | Humans | Index Medicus
Journal Article
Investigative ophthalmology & visual science, ISSN 0146-0404, 01/2013, Volume 54, Issue 1, pp. 387 - 387
Journal Article
Neuropediatrics, ISSN 0174-304X, 06/2017, Volume 48, Issue 3, pp. 185 - 187
Abstract Tadpole pupil is a rarely encountered phenomenon caused by episodic, segmental iris dilator muscle spasm of short duration (2–15 minutes), occurring... 
Short Communication | pathogenesis | denervation hypersensitivity | pediatric | tadpole pupil | HORNER-SYNDROME | IRIS DILATOR MUSCLE | SPASM | PEDIATRICS | CLINICAL NEUROLOGY
Journal Article
Genetics in Medicine, ISSN 1098-3600, 12/2011, Volume 13, Issue 12, pp. 1032 - 1041
Journal Article
Microbial Drug Resistance, ISSN 1076-6294, 09/2004, Volume 10, Issue 3, pp. 231 - 238
  In Denmark, tetracycline resistance in Streptococcus pyogenes is frequent (>30%) whereas macrolide resistance is low (<5%). The aim of this study was to... 
Macrolides | Humans | Genotype | Male | Colony Count, Microbial | Drug resistance | Tetracycline | Microbial Sensitivity Tests | Anti-Bacterial Agents | Drug Resistance, Multiple, Bacterial | Polymerase Chain Reaction | Genetics | Female | Streptococcus pyogenes
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