Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Robert H. Janigian"'
Publikováno v:
Journal of VitreoRetinal Diseases. 7:245-248
Purpose: To report a pediatric case of optic neuritis with subsequent development of central retinal vein occlusion (CRVO). Methods: A case and its findings were analyzed. Results: A 16-year-old boy presented with painful vision loss in the left eye,
Publikováno v:
CRO (Clinical & Refractive Optometry) Journal. 33
Background: Lyme Borreliosis accounts for less than 1% of all uveitis cases. The challenge in diagnosing Lyme-associated uveitis in a seropositive patient is determining whether the serology status is causative or incidental. We describe a case that
Publikováno v:
CRO (Clinical & Refractive Optometry) Journal. 32
Although uncommon, idiopathic retinal vasculitis, aneurysms, and neuroretinitis (IRVAN) syndrome can lead to vision threatening complications if not diagnosed and treated appropriately. This case report describes an atypical presentation of unilatera
Autor:
Victoria Branca, Amanda Hunter, Fatima Raposo, Paul B. Greenberg, Robert H. Janigian, Elina Goman-Baskin
Publikováno v:
CRO (Clinical & Refractive Optometry) Journal. 32
Purpose: To report a case of posterior scleritis presumed secondary to sarcoidosis. Results: A 79-year-old male with a history of sarcoidosis presented with asymptomatic conjunctival injection and chemosis of the right eye. The patient presumptively
Autor:
Rebecca E. MacDonell-Yilmaz, Jennifer J.G. Welch, Prabjot Channa, Brittney Statler, Robert H Janigian
Publikováno v:
JCO Oncology Practice. 16:139-141
Publikováno v:
Rhode Island medical journal (2013). 103(3)
A 41-year-old man presented to the emergency department with a painful and red left eye associated with chronic vision loss. He had a history of homelessness and polysubstance abuse including intravenous drug use. Fundus examination revealed several
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 23:59-61
We present the novel finding of retinal astrocytoma in a 15-year-old boy with phosphatase and tensin homologue hamartoma tumor syndrome, confirmed by genetic testing.
Publikováno v:
Rhode Island medical journal (2013). 102(6)
Neonatal-onset Multisystem Inflammatory Disorder (NOMID) is a systemic syndrome characterized by rash, large joint osteoarthropathies and chronic meningitis. Ocular manifestations include optic disc edema, corneal opacities and uveitis. We report the
Publikováno v:
Rhode Island medical journal (2013). 102(1)
[Full article available at http://rimed.org/rimedicaljournal-2019-02.asp].
Autor:
Janis Graul, Craig N. Kelso, Dennis B. Backes, Paul G. Arrigg, Collin L. DuCoty, John M. Bourg, David Emmert, Caldwell W. Smith, Helen K. Li, Ann Kopple, Robert H. Janigian, Terri Cain, Brian A. Rusinek, Donna J. Chesbrough, Susan Rath, Jennifer V. Helms, Michael J. Elman, Joe Fischer, Sheila M. Rock, Jo Ann Starr, Erika Banalewicz, Michelle Buck, Manjot K. Gill, Peter Sotirakos, Teresa Coffey, Paul M. Beer, Debbie M. Brown, David J. Browning, Judy E. Kim, Amy M. Flowers, Laima M. O'Donnell, Stephen T. Blevins, Giorya Shabi Andreani, Sylvia Varadian, Michele Melia, Charisse Whitney, Garvin H. Davis, Linda M. Davis, Allen McKinney, Susan B. Bressler, James L. Kinyoun, Michele E. Powers, Happy Spillar, Mary B. Savell, Jeanette Graf, Thomas W. Stone, Kenneth M. Huff, Janet Murphy, Judith L. Cruz, John W. Kitchens, Deborah K. Schlossman, Sandra U. Castillo, William J. Wood, Jeanne Van Arsdall, Roy W. Beck, Stacy Carpenter, Alex L. Nagle, Sandra Henriques, Jeffrey G. Gross, Edward A. Slade, Andrew N. Antoszyk, Heather L. Murphy, Joseph M. Googe, Harold A. Woodcome, Kelly A. Blackmer, Michelle D. Sloan, Jennifer K. Sun, Randall L. Price, Jon M. Braverman, Heidi K. Lovit, Timothy J. Murtha, Christina T. Higdon, Angella S. Karow, Adam R. Glassman, Julie P. Berry, Alice T. Lyon, Deborah Donohue, Loraine Clark, S. Shah, Joseph R. Beringer, Janelle Dane Zapata, Michael D. McOwen, Jonathan Shankle, Robert W. Cavicchi, Kimberly S. Walther, Eugenia Olmeda, Melissa K. Cowen, Joanne E. Bache, Leif S. Ryman, James D. Leslie, Denise Garza, Dennis P. Han, Karen Sjoblom, Margaret E. Stockman, Howard L. Cummings, Dawn Alvarez, Uma M. Balasubramaniam, Tracy A. Troszak, Brad C. Clifton, Paul A. Blais, Mary Frey, Paul A. Edwards, William J. Wirostko, Rosemary C. Rhodes, Clement K. Chan, Danielle R. Brooks, Theresa M. Butcher, K. M. Miller, Scott M. Friedman, Sasha I. Montalvo, Amber Crocker, Pamela V. Singletary, Sharon D. Solomon, Steve Carlton, Jolleen S. Key, Dawn M. Ryan, S. B. Bressler, L. Kaminski, Deanna Jo Long, Nancy Gore, Donna McClain, Magdalena G. Krzystolik, George S. Sharuk, Angela K. Price, Cecile Hunt, Antonio P. Ciardella, Lori E. Ackatz, Mark Hamel, Sandra West, Neil M. Bressler, Damanda A. Fagan, Judy Flanders
Publikováno v:
Eye. 26:833-840
To determine the rate of progression of eyes with subclinical diabetic macular edema (DME) to clinically apparent DME or DME necessitating treatment during a 2-year period. In all, 43 eyes from 39 study participants with subclinical DME, defined as a