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Journal of AAPOS, ISSN 1091-8531, 08/2018, Volume 22, Issue 4, pp. e3 - e3
Journal Article
Human Genetics, ISSN 0340-6717, 08/2019, pp. 1 - 4
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 2019, Volume 137, Issue 4, pp. 355 - 357
Ocular phenotypes of genetically determined eye disorders vary widely and overlap in physical findings and clinical appearance. This is particularly true of... 
OPHTHALMOLOGY | AXENFELD-RIEGER-SYNDROME | FOXC1 | MUTATIONS | PITX2 | Hypoplasia | Pax6 protein | Iris | Phenotypes | Congenital defects | Aniridia | Eye disorders | Retina | Index Medicus | Abridged Index Medicus
Journal Article
1998, Oxford monographs on medical genetics, ISBN 9780195096767, Volume no. 36, xv, 900
Book
Current Opinion in Ophthalmology, ISSN 1040-8738, 09/2019, Volume 30, Issue 5, pp. 306 - 313
PURPOSE OF REVIEWThe literature regarding prophylactic treatment of rhegmatogenous retinal detachment in Stickler syndrome remains controversial. We review... 
Index Medicus
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 03/2013, Volume 97, Issue 3, pp. 247 - 247
Journal Article
Journal of AAPOS, ISSN 1091-8531, 2016, Volume 20, Issue 4, pp. e39 - e39
Journal Article
Journal of AAPOS, ISSN 1091-8531, 08/2015, Volume 19, Issue 4, p. e73
Journal Article
Journal of AAPOS, ISSN 1091-8531, 08/2017, Volume 21, Issue 4, pp. e17 - e18
Journal Article
Journal of cataract and refractive surgery, ISSN 0886-3350, 12/2017, Volume 43, Issue 12, pp. 1611 - 1612
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 05/2017, Volume 38, Issue 3, pp. 299 - 299
Journal Article
07/2016, ISBN 9781493927449, 784
This case-based approach to the management of pediatric eye diseases and strabismus teaches the novice, as well as the experienced surgeon, how to... 
Pediatric ophthalmology | Clinical & internal medicine | Ophthalmology | Medicine & Public Health
eBook
Ophthalmology, ISSN 0161-6420, 2004, Volume 111, Issue 5, pp. 1035 - 1042
Purpose To outline the clinical features and surgical treatment of patients with familial and sporadic (simplex) forms of congenital fibrosis of extraocular... 
Manometry | Fibrosis - congenital | Eye Movements | Humans | Child, Preschool | Male | Blepharoptosis - diagnosis | Oculomotor Muscles - pathology | Ophthalmoplegia - classification | Visual Acuity | Blepharoptosis - surgery | Phenotype | Ophthalmoplegia - surgery | Oculomotor Muscles - surgery | Adolescent | Adult | Female | Aged | Ophthalmoplegia - genetics | Child | Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 331 - 339
Complete congenital stationary night blindness (cCSNB) is a clinically and genetically heterogeneous group of retinal disorders characterized by nonprogressive... 
COMPLETE FORM | LIGHT RESPONSE | CHANNEL | MGLUR6 | SYNAPTIC-TRANSMISSION | MOUSE MODEL | GENETICS & HEREDITY | NYCTALOPIN | RICH REPEAT PROTEIN | MUTATIONS | CONE ELECTRORETINOGRAM | Electroretinography - methods | Night Blindness - metabolism | Humans | Dark Adaptation - genetics | Retinal Rod Photoreceptor Cells - metabolism | Gene Knockdown Techniques - methods | Myopia - metabolism | Receptors, Metabotropic Glutamate - genetics | Retinal Bipolar Cells - physiology | Chromosome Mapping - methods | Genetic Diseases, X-Linked | Night Blindness - genetics | Retinal Bipolar Cells - metabolism | Eye Diseases, Hereditary | Signal Transduction | Mice, Inbred C57BL | Zebrafish | Mice, Inbred C3H | Myopia - genetics | Animals | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Retinal Rod Photoreceptor Cells - physiology | Heterozygote | Mice | Receptors, G-Protein-Coupled - genetics | Mutation | Chromosome mapping | Usage | Gene mutations | Retinal bipolar cells | Causes of | Physiological aspects | Night blindness | Genetic aspects | Research | Analysis | Genetic disorders | Proteins | Rodents | Blindness | Gene expression | Cells | Index Medicus | Animal models | Antibodies | Insertion | stationary night blindness | Retina | Guanine nucleotide-binding protein | Electroretinograms | Depolarization | Signal transduction | Vision | Bipolar cells | Gene mapping | DNA sequencing | Report
Journal Article
OPHTHALMIC SURGERY LASERS & IMAGING RETINA, ISSN 2325-8160, 06/2019, Volume 50, Issue 6, pp. E188 - E192
Choroidal neovascular membrane (CNVM) is a rare complication of choroideremia. The authors report a case of a 13-year-old male presenting with metamorphopsia... 
SURGERY | OPHTHALMOLOGY | COHERENCE TOMOGRAPHY-ANGIOGRAPHY
Journal Article
Journal of AAPOS, ISSN 1091-8531, 08/2017, Volume 21, Issue 4, pp. e55 - e56
Journal Article
Journal of AAPOS, ISSN 1091-8531, 2015, Volume 19, Issue 4, pp. e73 - e73
Journal Article
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