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Anil Kumar Mandal

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Ophthalmology|March 31, 2004
Glaucoma in southern IndiaRavi Thomas, Chandrasekhar Garudadri, Anil Kumar Mandal, et al.
Journal of Pediatric Ophthalmology and Strabismus|December 28, 2013
Clinical manifestations of congenital aniridiaBhupesh 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 IndiaSreelatha Komatireddy, Subhabrata Chakrabarti, Anil Kumar Mandal, et al.
Molecular Vision|October 12, 2004
Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patientsAramati 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 glaucomaDivya 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 ChildrenMuralidhar 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 glaucomaArijit Mukhopadhyay, Sreelatha Komatireddy, Moulinath Acharya, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Ophthalmology|March 31, 2004
Glaucoma in southern IndiaRavi Thomas, Chandrasekhar Garudadri, Anil Kumar Mandal, et al.
Journal of Pediatric Ophthalmology and Strabismus|December 28, 2013
Clinical manifestations of congenital aniridiaBhupesh 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 IndiaSreelatha Komatireddy, Subhabrata Chakrabarti, Anil Kumar Mandal, et al.
Molecular Vision|October 12, 2004
Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patientsAramati 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 glaucomaDivya 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 ChildrenMuralidhar 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 glaucomaArijit Mukhopadhyay, Sreelatha Komatireddy, Moulinath Acharya, et al.
Pageof 2