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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 1
2010 4
2011 3
2012 5
2013 8
2014 1
2015 2
2016 3
2017 2
2019 1
2022 2
2024 0

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28 results

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Page 1
Genomics of rare genetic diseases-experiences from India.
GUaRDIAN Consortium; Sivasubbu S, Scaria V. GUaRDIAN Consortium, et al. Hum Genomics. 2019 Sep 25;14(1):52. doi: 10.1186/s40246-019-0215-5. Hum Genomics. 2019. PMID: 31554517 Free PMC article. Review.
The catatonia conundrum: controversies and contradictions.
Padhy SK, Parakh P, Sridhar M. Padhy SK, et al. Among authors: parakh p. Asian J Psychiatr. 2014 Feb;7(1):6-9. doi: 10.1016/j.ajp.2013.07.006. Epub 2013 Aug 22. Asian J Psychiatr. 2014. PMID: 24524702 Review.
Speech rhythm in Kannada speaking adults who stutter.
Maruthy S, Venugopal S, Parakh P. Maruthy S, et al. Among authors: parakh p. Int J Speech Lang Pathol. 2017 Oct;19(5):529-537. doi: 10.1080/17549507.2016.1221459. Epub 2016 Aug 30. Int J Speech Lang Pathol. 2017. PMID: 27576027
Mephentermine dependence: an emerging challenge.
Kumar Mattoo S, Parakh P. Kumar Mattoo S, et al. Among authors: parakh p. CNS Neurosci Ther. 2012 Jun;18(6):509-10. doi: 10.1111/j.1755-5949.2012.00328.x. CNS Neurosci Ther. 2012. PMID: 22672305 Free PMC article. No abstract available.
The many faces of trichotillomania.
Parakh P, Srivastava M. Parakh P, et al. Int J Trichology. 2010 Jan;2(1):50-2. doi: 10.4103/0974-7753.66916. Int J Trichology. 2010. PMID: 21188027 Free PMC article.
Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study.
Sinha R, Pradhan S, Banerjee S, Jahan A, Akhtar S, Pahari A, Raut S, Parakh P, Basu S, Srivastava P, Nayak S, Thenral SG, Ramprasad V, Ashton E, Bockenhauer D, Mandal K. Sinha R, et al. Among authors: parakh p. Pediatr Nephrol. 2022 Aug;37(8):1811-1836. doi: 10.1007/s00467-021-05388-y. Epub 2022 Jan 10. Pediatr Nephrol. 2022. PMID: 35006361
28 results