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- Publications
- Influence
An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract.
- G. Senthil Kumar, J. Kyle, +5 authors S. Santhiya
- Biology, Medicine
- Experimental eye research
- 1 May 2013
Autosomal dominant congenital cataracts have been associated with mutations of genes encoding several soluble and membrane proteins. By candidate gene screening, we identified a novel mutation in MIP… Expand
Comparison of trapezius squeeze test and jaw thrust as clinical indicators for laryngeal mask airway insertion in spontaneously breathing children
- K. D. Dinesh Kumar, N. Bhardwaj, S. Yaddanapudi
- Medicine
- Journal of anaesthesiology, clinical pharmacology
- 2017
Background and Aims: It is not known whether trapezius squeeze test (TPZ) is a better clinical test than jaw thrust (JT) to assess laryngeal mask airway (LMA) insertion conditions in children under… Expand
The E368Q Mutant Allele of GJA8 is Associated with Congenital Cataracts with Intrafamilial Variation in a South Indian Family.
- G. Senthil Kumar, K. D. Dinesh Kumar, +4 authors S. T. Santhiya
- Biology, Medicine
- Open access journal of ophthalmology
- 2016
PURPOSE
To determine the basis of the autosomal dominant congenital cataracts in a three generation south Indian pedigree.
METHODS
The proband and several family members underwent a complete… Expand
Impact of Vedic Chants Intervention Programme on Autistic Spectrum Disorder
- K. D. Dinesh Kumar, Sushruth Badhe, S. Santhiya
- Medicine
- Molecular Cytogenetics
- 21 January 2014
Background Autism Spectrum Disorder (ASD) is a developmental disorder that affects the behavior and social communication of the child. In India, awareness about Autism coupled with shortage of… Expand