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Genetic analysis of ATP7B in 102 south Indian families with Wilson disease.
Singh N, Kallollimath P, Shah MH, Kapoor S, Bhat VK, Viswanathan LG, Nagappa M, Bindu PS, Taly AB, Sinha S, Kumar A. Singh N, et al. Among authors: bindu ps. PLoS One. 2019 May 6;14(5):e0215779. doi: 10.1371/journal.pone.0215779. eCollection 2019. PLoS One. 2019. PMID: 31059521 Free PMC article.
Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex.
Kapoor S, Shah MH, Singh N, Rather MI, Bhat V, Gopinath S, Bindu PS, Taly AB, Sinha S, Nagappa M, Bharath RD, Mahadevan A, Narayanappa G, Chickabasaviah YT, Kumar A. Kapoor S, et al. Among authors: bindu ps. PLoS One. 2016 May 19;11(5):e0155605. doi: 10.1371/journal.pone.0155605. eCollection 2016. PLoS One. 2016. PMID: 27196560 Free PMC article.
Panda with "Bright eyes" in Wilson's disease.
Kallollimath P, Nagappa M, Sinha S, Saini J, Bindu PS, Taly AB. Kallollimath P, et al. Among authors: bindu ps. Neurol India. 2013 Jan-Feb;61(1):100-1. doi: 10.4103/0028-3886.108052. Neurol India. 2013. PMID: 23466863 Free article. No abstract available.
Oculomotor apraxia in Gaucher disease.
Nagappa M, Bindu PS, Taly AB, Sinha S. Nagappa M, et al. Among authors: bindu ps. Pediatr Neurol. 2015 Apr;52(4):468-9. doi: 10.1016/j.pediatrneurol.2014.10.016. Epub 2014 Oct 18. Pediatr Neurol. 2015. PMID: 25687160 No abstract available.
Audiological findings in Infantile Refsum disease.
Vandana VP, Bindu PS, Nagappa M, Sinha S, Taly AB. Vandana VP, et al. Among authors: bindu ps. Int J Pediatr Otorhinolaryngol. 2015 Aug;79(8):1366-9. doi: 10.1016/j.ijporl.2015.05.023. Epub 2015 May 30. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26055198
119 results