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Ophthalmology
|
March 31, 2004
Glaucoma in southern India
Ravi Thomas, Chandrasekhar Garudadri, Anil Kumar Mandal, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
December 28, 2013
Clinical manifestations of congenital aniridia
Bhupesh Singh, Ashik Mohamed, Sunita Chaurasia, et al.
Molecular Vision
|
February 20, 2003
Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India
Sreelatha Komatireddy, Subhabrata Chakrabarti, Anil Kumar Mandal, et al.
Molecular Vision
|
October 12, 2004
Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients
Aramati Bindu Madhava Reddy, Kiranpreet Kaur, Anil Kumar Mandal, et al.
Indian Journal of Ophthalmology
|
December 1, 2022
Objectively measuring anterior segment alterations in the eyes of mucopolysaccharidoses: Its utility in early diagnosis of glaucoma
Divya Sree Ramya Achanta, Ashik Mohamed, Sunita Chaurasia, et al.
Cornea
|
October 5, 2022
Selective Endothelialectomy in Peters Anomaly: A Novel Surgical Technique and Its Clinical Outcomes in Children
Muralidhar Ramappa, Sunita Chaurasia, Ashik Mohamed, et al.
Molecular Vision
|
October 6, 2005
Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma
Arijit Mukhopadhyay, Sreelatha Komatireddy, Moulinath Acharya, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
Ophthalmology
|
March 31, 2004
Glaucoma in southern India
Ravi Thomas, Chandrasekhar Garudadri, Anil Kumar Mandal, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
December 28, 2013
Clinical manifestations of congenital aniridia
Bhupesh Singh, Ashik Mohamed, Sunita Chaurasia, et al.
Molecular Vision
|
February 20, 2003
Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India
Sreelatha Komatireddy, Subhabrata Chakrabarti, Anil Kumar Mandal, et al.
Molecular Vision
|
October 12, 2004
Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients
Aramati Bindu Madhava Reddy, Kiranpreet Kaur, Anil Kumar Mandal, et al.
Indian Journal of Ophthalmology
|
December 1, 2022
Objectively measuring anterior segment alterations in the eyes of mucopolysaccharidoses: Its utility in early diagnosis of glaucoma
Divya Sree Ramya Achanta, Ashik Mohamed, Sunita Chaurasia, et al.
Cornea
|
October 5, 2022
Selective Endothelialectomy in Peters Anomaly: A Novel Surgical Technique and Its Clinical Outcomes in Children
Muralidhar Ramappa, Sunita Chaurasia, Ashik Mohamed, et al.
Molecular Vision
|
October 6, 2005
Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma
Arijit Mukhopadhyay, Sreelatha Komatireddy, Moulinath Acharya, et al.
Page
of 2