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Parkin mutations in familial and sporadic Parkinson's disease among Indians.
Chaudhary S, Behari M, Dihana M, Swaminath PV, Govindappa ST, Jayaram S, Goyal V, Maitra A, Muthane UB, Juyal RC, Thelma BK. Chaudhary S, et al. Parkinsonism Relat Disord. 2006 May;12(4):239-45. doi: 10.1016/j.parkreldis.2005.12.004. Epub 2006 Feb 24. Parkinsonism Relat Disord. 2006. PMID: 16500134
Complex phenotypes in an Indian family with homozygous SCA2 mutations.
Ragothaman M, Sarangmath N, Chaudhary S, Khare V, Mittal U, Sharma S, Komatireddy S, Chakrabarti S, Mukerji M, Juyal RC, Thelma BK, Muthane UB. Ragothaman M, et al. Among authors: chaudhary s. Ann Neurol. 2004 Jan;55(1):130-3. doi: 10.1002/ana.10815. Ann Neurol. 2004. PMID: 14705123
NCCP-ICS joint consensus-based clinical practice guidelines on medical thoracoscopy.
Chawla RK, Kumar M, Madan A, Dhar R, Gupta R, Gothi D, Desai U, Goel M, Swarankar R, Nene A, Munje R, Chaudhary D, Guleria R, Hadda V, Nangia V, Sindhwani G, Chawla R, Dutt N, Yuvarajan, Dalal S, Gaur SN, Katiyar S, Samaria JK, Gupta KB, Koul PA, Suryakant, Christopher DJ, Roy D, Hazarika B, Luhadia SK, Jaiswal A, Madan K, Gupta PP, Prashad BNBM, Yusuf N, James P, Dhamija A, Tomar V, Parakh U, Khan A, Garg R, Singh S, Joshi V, Sarangdhar N, Chaudhary SR, Nayar S, Patel A, Gupta M, Dixit RK, Jain S, Gogia P, Agarwal M, Katiyar S, Chawla A, Gonuguntala HK, Dosi R, Chinnamchetty V, Jindal A, Sharma S, Chachra V, Samaria U, Nair A, Mohan S, Maitra G, Sinha A, Kochar R, Yadav A, Choudhary G, Arunachalam M, Rangarajan A, Sanjan G. Chawla RK, et al. Among authors: chaudhary sr. Lung India. 2024 Mar 1;41(2):151-167. doi: 10.4103/lungindia.lungindia_5_24. Epub 2024 Feb 27. Lung India. 2024. PMID: 38700413 Free PMC article.
1,667 results