Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Anmol U Naik"'
Publikováno v:
Indian Journal of Ophthalmology, Vol 67, Iss 6, Pp 732-739 (2019)
Vitreous hemorrhage is one of the most common causes of sudden, painless loss of vision in adults. This is probably one of the reasons why it has been extensively studied and reported in literature. However, the same cannot be said when it comes to v
Externí odkaz:
https://doaj.org/article/911dd7c7d95347c294b7a7c78988c1a3
Publikováno v:
Oman Journal of Ophthalmology, Vol 12, Iss 1, Pp 62-64 (2019)
A 23-year male with complaint of diminution of vision in left eye was referred to us as a suspect case of inflammatory choroidal mass/melanoma. Examination revealed a total retinal detachment with a reddish brown lesion in the superior hemi-fundus. B
Externí odkaz:
https://doaj.org/article/faeb5a97bffe46cea135790e9ac4a24a
Publikováno v:
Indian Journal of Ophthalmology, Vol 66, Iss 10, Pp 1483-1485 (2018)
The classic entity of autosomal dominant Blau syndrome (BS) consists of arthritis, dermatitis, and uveitis, occurring as a result of mutations in the NOD2 gene pattern recognition receptor. Sporadic cases are those in which no known gene mutation is
Externí odkaz:
https://doaj.org/article/3671bcf403ac44f4abcd0e13c050d272
Publikováno v:
Indian Journal of Ophthalmology, Vol 66, Iss 8, Pp 1200-1202 (2018)
A 60-year-old male presented with pain and decreased vision 3 weeks following uneventful intracapsular cataract extraction with anterior vitrectomy for subluxated cataract. A diagnosis of acute endophthalmitis was made based on clinical and ultrasoun
Externí odkaz:
https://doaj.org/article/1563102a3a5d40ba8162a75188ac01d4
Publikováno v:
Indian Journal of Ophthalmology, Vol 66, Iss 11, Pp 1637-1639 (2018)
A 44-year-old female presented with central vision loss and photopsia in both eyes since 2 months. Multimodal imaging, field defects, electroretinogram abnormalities, and spectral domain optical coherence tomography changes were all suggestive of acu
Externí odkaz:
https://doaj.org/article/2930307ce62141b2858af5e13f3055ec
Publikováno v:
Indian Journal of Ophthalmology, Vol 67, Iss 4, Pp 556-556 (2019)
Externí odkaz:
https://doaj.org/article/0e0104093d994f10a6e80ebbff831bf7
Publikováno v:
Indian Journal of Ophthalmology
Indian Journal of Ophthalmology, Vol 66, Iss 10, Pp 1483-1485 (2018)
Indian Journal of Ophthalmology, Vol 66, Iss 10, Pp 1483-1485 (2018)
The classic entity of autosomal dominant Blau syndrome (BS) consists of arthritis, dermatitis, and uveitis, occurring as a result of mutations in the NOD2 gene pattern recognition receptor. Sporadic cases are those in which no known gene mutation is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e1f694ed8ed46ad071f6fe9c8977eb9
http://europepmc.org/articles/PMC6173012
http://europepmc.org/articles/PMC6173012
Publikováno v:
Indian Journal of Ophthalmology
Indian Journal of Ophthalmology, Vol 66, Iss 11, Pp 1637-1639 (2018)
Indian Journal of Ophthalmology, Vol 66, Iss 11, Pp 1637-1639 (2018)
A 44-year-old female presented with central vision loss and photopsia in both eyes since 2 months. Multimodal imaging, field defects, electroretinogram abnormalities, and spectral domain optical coherence tomography changes were all suggestive of acu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50cfe0ff6b21ca2c90778f2eecf28858
http://europepmc.org/articles/PMC6213690
http://europepmc.org/articles/PMC6213690
Autor:
Rajiv Raman, Anmol U Naik
Publikováno v:
JAMA Ophthalmology. 138:e190059
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd5c620c234dc0b80fb29187e6e71455
https://doi.org/10.1001/jamaophthalmol.2019.0059
https://doi.org/10.1001/jamaophthalmol.2019.0059
Autor:
Anmol U Naik, Jaydeep Walinjkar, Pradeep Susvar, Girish Shiva Rao, Muna Bhende, Chetan Rao, Parveen Sen, V Jayaprakash, Dhanashree Ratra, Daleena Dalan, Aniruddha Banerjee, Sourabh Jandyal
Publikováno v:
Indian Journal of Ophthalmology, Vol 67, Iss 4, Pp 523-529 (2019)
Indian Journal of Ophthalmology
Indian Journal of Ophthalmology
Purpose: Enhanced S-cone syndrome (ESCS), a rare disorder, is often misdiagnosed as other forms of retinal degenerations, which have a poorer prognosis than ESCS. The aim of this study is to report the varied clinical features of ESCS and distinguish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1299b0714215f71f16bd6ee823ad5d3e
https://doi.org/10.4103/ijo.ijo_1480_18
https://doi.org/10.4103/ijo.ijo_1480_18