Vaishnavi Batmanabane
Toronto, ON M5G1X8, Canada
Last Updated: 09/26/2026
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Found 11 publications
IFT80 mutations cause a novel complex ciliopathy phenotype with retinal degeneration.
Journal: Clinical genetics
Published: April 04, 2018
C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations.
Journal: Investigative ophthalmology & visual science
Published: August 02, 2017
The combination of vestibular impairment and congenital sensorineural hearing loss predisposes patients to ocular anomalies, including Usher syndrome.
Journal: Clinical genetics
Published: August 03, 2016
The role of MR imaging in investigating isolated pediatric nystagmus.
Journal: Pediatric radiology
Published: December 03, 2015
An infraumbilical lump in a child.
Journal: Emergency medicine journal : EMJ
Published: November 24, 2015
Liver anomalies as a phenotype parameter of Bardet-Biedl syndrome.
Journal: Clinical genetics
Published: July 23, 2015
Morphological patterns of indirect choroidal rupture on spectral domain optical coherence tomography.
Journal: Clinical ophthalmology (Auckland, N.Z.)
Published: August 01, 2013
Steroids in leptospiral uveitis: Does the route of administration matter?
Journal: Journal of pharmacology & pharmacotherapeutics
Published: February 28, 2012
Spectrum of Leptospira species identified in patients with leptospiral uveitis in an ophthalmological institute in South India.
Journal: Indian journal of medical microbiology
Published: November 29, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026