Smith-Lemli-Opitz Syndrome: Neuropathological and Ophthalmological Observations
Author:
Publisher
Wiley
Subject
Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1977.tb08021.x/fullpdf
Reference12 articles.
1. Opsoclonus in infancy;Bienfang;Archives of Ophthalmology,1974
2. The coincidence of neuroblastoma and acute cerebellar encephalopathy;Bray;Journal of Pediatrics,1969
3. Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome)-clinical features and mode of inheritance;Dallaire;Journal of Medical Genetics,1969
4. Opsoclonus and parenchymatous degeneration of the cerebellum. The cerebellar origin of an abnormal ocular movement;Ellenberger;Neurology,1968
5. Ocular dyskinesia in cerebellar disease: evidence for the similarity of opsoclonus, ocular dysmetria and flutter-like oscillations;Ellenberger;Brain,1972
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