Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Piero, Carletti"'
Autor:
Mariana Abi Karam, Arjun Sharma, Ashley Lopez-Canizares, Piero Carletti, Elizabeth A. Vanner, Audina M. Berrocal, Ta Chen Chang
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-6 (2024)
Abstract We conducted a retrospective review of patients (
Externí odkaz:
https://doaj.org/article/42d97a10645747d4a61a3786309ae9de
Autor:
Piero Carletti, Aaditya Shah, Christopher Bair, Christian Curran, Anthony Mai, Rachel Patel, Ramana Moorthy, Natalia Villate, Janet L. Davis, Albert T. Vitale, Akbar Shakoor, Lynn Hassman
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 31, Iss , Pp 101857- (2023)
Purpose: Although conjunctivitis represents the most common ocular manifestation of COVID-19 infection, sight-threatening retinal involvement has been reported. Herein, we report and characterize with multimodal retinal imaging 5 cases of acute visio
Externí odkaz:
https://doaj.org/article/d0976415c09a441cb24eda0728dcacad
Autor:
Julia Hudson, Hasenin Al-khersan, Piero Carletti, Darlene Miller, Sander R. Dubovy, Guillermo Amescua
Publikováno v:
Curr Opin Ophthalmol
PURPOSE OF REVIEW: To review the existing literature and investigate the role of microbiologic culture and histopathologic examination of corneal biopsies in the management of infectious keratitis. RECENT FINDINGS: Corneal biopsy continues to be a si
Autor:
Ashley, Lopez-Cañizares, Hasenin, Al-Khersan, Piero, Carletti, Carol L, Shields, Audina M, Berrocal
Publikováno v:
Ophthalmic Surgery, Lasers and Imaging Retina. 53:514-516
Gorlin syndrome is a rare autosomal dominant disorder with near complete penetrance. The underlying genetic mechanism is a mutation in a tumor suppressor gene. Thus far, mutations in patched homolog 1 and 2 genes (PTCH1 and PTCH2) and the suppressor
Autor:
Piero Carletti, Paula A. Sepulveda Beltran, Harry Levine, Sander R. Dubovy, Victor L. Perez, Guillermo Amescua
Publikováno v:
Ocular immunology and inflammation.
To describe the long-term management of bilateral limbal stem cell deficiency secondary to a severe chemical burn.Descriptive case report.This case highlights the importance of early intervention in ocular chemical burns for the preservation of tissu
Publikováno v:
JAMA ophthalmology. 140(8)
A 9-year-old girl with a history of neonatal seizures presents to a pediatric retina service with progressive vision loss. What would you do next?
Autor:
Ashley López-Cañizares, Maria P. Fernandez, Hasenin Al-Khersan, Piero Carletti, Monica S Arroyo, Maria C Fernandez-Ruiz, Audina M Berrocal
Publikováno v:
Ophthalmic genetics. 43(4)
Coats plus syndrome or cerebroretinal microangiopathy with calcifications and cysts (CMCC) is an exceedingly rare autosomal recessive disorder that predominantly affects the microvasculature in the retina, brain, bones, and gastrointestinal system. U
Publikováno v:
JAMA Ophthalmology. 140:1015
A 9-year-old boy presented with changes in peripheral retinal pigment epithelium. Ocular history included high hyperopia and amblyopia, and abnormal foveal contour was discovered when he was aged 3 years. What would you do next?
Publikováno v:
Med Sci Educ
INTRODUCTION: Medical education is oftentimes stressful and has been documented to compromise student well-being, hinder performance, and contribute to burnout. Many medical schools aim to foster students’ sense of well-being. This can be accomplis
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