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Articles by V. Sreenivas
A split‐tattoo randomized QS Nd‐YAG laser trial comparing the efficacy of R15 method with conventional regime in the treatment of blue/black tattoos in darker skin types
CONCISE REPORT A. Narayanan, orcid.org/0000-0003-2832-5299 Departments of Dermatology, All India Institute of Medical Sciences, New Delhi, 110 029 India Search for more papers by this author N. Bhari, orcid.org/0000-0002-4604-3917 Departments of Dermatology, All India Institute of Medical Sciences, New Delhi, 110 029 India Search for more papers by this author V.
Evaluation of ‘Not relevant’ responses on the DLQI, and the DLQI‐R scoring modification among Indian patients with vitiligo
RESEARCH LETTER V.
Determining the minimal important change scores of the Vitiligo Impact Scale (VIS)‐22 and Dermatology Life Quality Index (DLQI) scores in Indian patients with vitiligo using anchor‐ and distribution‐based approaches
This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as doi:10.1111/bjd.18984
Correlation between Non-Polio Acute Flaccid Paralysis Rates with Pulse Polio Frequency in India
Rachana Dhiman,1 Sandeep C. Prakash,1 V. Sreenivas,2 and Jacob Puliyel1,* Rachana Dhiman 1Department of Pediatrics, St Stephens Hospital, Delhi 110054, India; moc.liamg@84anhcarnamihd (R.D.); moc.liamg@52ppcpeednas (S.C.P.) Sandeep C.
Correlation between Non-Polio Acute Flaccid Paralysis Rates with Pulse Polio Frequency in India
The last case of polio from India was reported in 2011. That year, the non-polio acute flaccid paralysis (NPAFP) rate in India was 13.35/100,000, where the expected rate is 1–2/100,000. A previous study of data from 2000 to 2010 has detailed the NPAFP rate in a state correlated with the pulse polio rounds conducted there, and the strongest correlation with the NPAFP rate was found when the number of doses from the previous 4 years were used.
Development of a Clinical Diagnostic Matrix for characterising Inherited Epidermolysis Bullosa
Accurately diagnosing the subtype of Epidermolysis Bullosa (EB) is critical for management and genetic counseling. Modern laboratory techniques are largely inaccessible in developing countries, where the diagnosis remains clinical and often inaccurate. To develop a simple clinical diagnostic tool to aid in the diagnosis and sub typing of EB. We developed a matrix indicating presence or absence of a set of distinctive clinical features (rows) for the 9 more prevalent EB subtypes (columns).
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