Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jacqueline M S Winterkorn"'
Publikováno v:
Neuro-Ophthalmology. 16:163-170
We present five patients who developed luxury perfusion following anterior ischemic optic neuropathy in whom fluorescein angiography was misinterpreted as "capillary hemangioma" or neovascularization of the disc. In each case, the segment of disc hyp
Autor:
Andrew J Levada, Jacqueline M S Winterkorn, Jonathan E. Silbert, Christina Rapp Prescott, Robert L. Lesser, M Joshua Hasbani
Publikováno v:
Journal of Pediatric Ophthalmology & Strabismus. 48
The authors describe four patients with Parry–Romberg syndrome (PRS) who had abnormal eye movements, ptosis, and facial hemiatrophy. There were delays in diagnosis in all cases, often requiring multiple imaging studies, prior to diagnosis of PRS. T
Publikováno v:
International Ophthalmology Clinics. 33:169-178
Autor:
Jacqueline M. S. Winterkorn
Publikováno v:
Archives of ophthalmology (Chicago, Ill. : 1960). 110(6)
Publikováno v:
Neurology. 41(8)
In four of six patients with clinical optic chiasmal neuritis, MRI demonstrated abnormalities of the chiasm. Optic chiasmal neuritis may be the initial manifestation of multiple sclerosis, a reflection of established CNS demyelination, or an isolated
Autor:
Jacqueline M. S. Winterkorn
Publikováno v:
Archives of Ophthalmology. 115:943
Publikováno v:
Journal of Neuro-Ophthalmology. 16:163
Autor:
Lionel U. Mailloux, Barbara Napolitano, Wilhelm Vetter, Jacqueline M. S. Winterkorn, Klara Landau
Publikováno v:
Archives of Ophthalmology. 114:570
Objective: To define parameters of ambulatory diurnal blood pressure in patients who had experienced anterior ischemic optic neuropathy (AION) in a case-controlled study. Participants and Methods: Twenty-four patients with AION and 24 control subject
Autor:
Jacqueline M. S. Winterkorn
Publikováno v:
Archives of Ophthalmology. 113:1464
Publikováno v:
Archives of Ophthalmology. 111:219
Selective downgaze paralysis was correlated with discrete bilateral lesions at the mesencephalic-diencephalic junction in a 9-year-old girl following severe pneumococcal meningitis, and in a 64-year-old man who suffered an embolic infarction. Magneti