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Arundhati Sharma

Researcher at All India Institute of Medical Sciences

Publications -  249
Citations -  1901

Arundhati Sharma is an academic researcher from All India Institute of Medical Sciences. The author has contributed to research in topics: Cancer & Single-nucleotide polymorphism. The author has an hindex of 20, co-authored 234 publications receiving 1591 citations. Previous affiliations of Arundhati Sharma include AIIMS, New Delhi.

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Sutureless and glue-free conjunctival autograft in pterygium surgery: a case series

TL;DR: This simple technique for pterygium surgery may prevent potential adverse reactions encountered with the use of foreign materials and in this small series provided safe and comparable results to current methods.
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Study of clinical, biochemical and immunological factors determining stability of disease in patients with generalized vitiligo undergoing melanocyte transplantation.

TL;DR: A large number of patients with vitiligo have undergone at least one melanocyte transplantation procedure in the past and current criteria rely on the history given by the patients, so it is necessary to assess the need for further studies on this basis.
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Oxidative stress and ATPase6 mutation is associated with primary ovarian insufficiency

TL;DR: This pilot study clearly demonstrates for the first time ATPase6 gene nucleotide alterations and elevated ROS levels in idiopathic cases of POI and it may be possible that OS associated with ATPase 6 gene mutation may be causal in Idiopathics cases of premature OI.
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Alteration in regulatory T cells and programmed cell death 1-expressing regulatory T cells in active generalized vitiligo and their clinical correlation

TL;DR: Vitiligo is an autoimmune depigmentation disease, and defects in regulatory T cells (Tregs) have been proposed in the pathogenesis of generalized vitiligo, but the role of programmed cell death (PD)1+ Tregs has not been studied.
Journal Article

A novel VSX1 mutation identified in an individual with keratoconus in India

TL;DR: This is the first report from the Indian subcontinent exploring the role of VSX1 in the causation of keratoconus and one novel mutation predicted to be a potentially damaging change was seen in an affected individual.