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International Journal of Neuroscience, ISSN 0020-7454, 02/2019, Volume 129, Issue 2, pp. 103 - 109
Journal Article
Neurology, ISSN 0028-3878, 06/2016, Volume 86, Issue 23, pp. 2214 - 2215
Journal Article
Journal Article
Neurology, ISSN 0028-3878, 06/2015, Volume 84, Issue 22, pp. 2291 - 2291
Following a whiplash injury, a previously healthy 33-year-old man complained of altered hearing in his right ear. While humming, he noticed a disturbing... 
CLINICAL NEUROLOGY | Nystagmus, Pathologic - complications | Nystagmus, Pathologic - diagnosis | Humans | Dizziness - diagnosis | Adult | Dizziness - complications | Male | Head-Down Tilt | Index Medicus | Abridged Index Medicus
Journal Article
Molecular Vision, ISSN 1090-0535, 01/2015, Volume 21, pp. 88 - 97
Purpose: Aniridia is a rare panocular disorder characterized by iris hypoplasia and other associated eye anomalies. Heterozygous null mutations in paired box... 
DEFECTS | NONSENSE | DNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | OPHTHALMOLOGY | MESSENGER-RNA DECAY | PAX6 GENE | DELETIONS | MISSENSE MUTATIONS | PREDICTION | REGION | Iris - metabolism | Humans | Middle Aged | Cataract - pathology | Child, Preschool | Fovea Centralis - pathology | Male | Nystagmus, Congenital - genetics | Aniridia - genetics | Aniridia - pathology | DNA Mutational Analysis | Nystagmus, Pathologic - complications | Base Sequence | Child | Amino Acid Sequence | Eye Diseases, Hereditary - pathology | Eye Diseases, Hereditary - complications | Repressor Proteins - genetics | Aniridia - complications | Genetic Heterogeneity | India | Cataract - complications | Adolescent | Cataract - genetics | Mutation | Glaucoma - genetics | Paired Box Transcription Factors - genetics | Retinal Diseases - genetics | Nystagmus, Congenital - complications | Nystagmus, Pathologic - genetics | Open Reading Frames | Molecular Sequence Data | Infant | Retinal Diseases - congenital | Case-Control Studies | Retinal Diseases - pathology | Adult | Female | Eye Proteins - genetics | Nystagmus, Pathologic - pathology | Fovea Centralis - abnormalities | Genetic Association Studies | Introns | Retinal Diseases - complications | PAX6 Transcription Factor | Glaucoma - complications | Iris - pathology | Homeodomain Proteins - genetics | Eye Diseases, Hereditary - genetics | Haploinsufficiency | Nystagmus, Congenital - pathology | Aged | Glaucoma - pathology | Index Medicus
Journal Article
Neurological Sciences, ISSN 1590-1874, 8/2017, Volume 38, Issue 8, pp. 1543 - 1545
Journal Article
Neurology, ISSN 0028-3878, 03/2013, Volume 80, Issue 13, pp. 1261 - 1262
Journal Article
Journal of Neurology, ISSN 0340-5354, 6/2013, Volume 260, Issue 6, pp. 1489 - 1496
Journal Article
Journal Article
Canadian Journal of Ophthalmology, ISSN 0008-4182, 2016, Volume 52, Issue 2, pp. 203 - 206
Abstract Objective To evaluate the outcomes of cataract surgery in pediatric patients presenting with bilateral infantile cataracts and nystagmus. Design... 
Internal Medicine | Ophthalmology | SURGERY | OPHTHALMOLOGY | CONGENITAL CATARACTS | CHILDREN | Follow-Up Studies | Humans | Infant | Male | Treatment Outcome | Nystagmus, Pathologic - physiopathology | Visual Acuity | Cataract - complications | Time Factors | Nystagmus, Pathologic - complications | Cataract Extraction - methods | Female | Retrospective Studies | Index Medicus
Journal Article