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Year Number of Results
2009 1
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2014 9
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2017 11
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2019 11
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2022 28
2023 19
2024 33
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168 results

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Page 1
Consensus Guidelines on Management of Steroid-Resistant Nephrotic Syndrome.
Vasudevan A, Thergaonkar R, Mantan M, Sharma J, Khandelwal P, Hari P, Sinha A, Bagga A; Expert Group Of The Indian Society Of Pediatric Nephrology. Vasudevan A, et al. Indian Pediatr. 2021 Jul 15;58(7):650-666. Epub 2021 Jan 4. Indian Pediatr. 2021. PMID: 33408286 Free article.
Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India.
Narang A, Uppilli B, Vivekanand A, Naushin S, Yadav A, Singhal K, Shamim U, Sharma P, Zahra S, Mathur A, Seth M, Parveen S, Vats A, Hillman S, Dolma P, Varma B, Jain V; TRISUTRA Ayurgenomics Consortium; Prasher B, Sengupta S, Mukerji M, Faruq M. Narang A, et al. Among authors: faruq m. Hum Mutat. 2020 Nov;41(11):1833-1847. doi: 10.1002/humu.24102. Epub 2020 Sep 9. Hum Mutat. 2020. PMID: 32906206
Prognostic evaluation of quick sequential organ failure assessment score in ICU patients with sepsis across different income settings.
Li A, Ling L, Qin H, Arabi YM, Myatra SN, Egi M, Kim JH, Nor MBM, Son DN, Fang WF, Wahyuprajitno B, Hashmi M, Faruq MO, Patjanasoontorn B, Al Bahrani MJ, Shrestha BR, Shrestha U, Nafees KMK, Sann KK, Palo JEM, Mendsaikhan N, Konkayev A, Detleuxay K, Chan YH, Du B, Divatia JV, Koh Y, Phua J; MOSAICS II Study Group; Asian Critical Care Clinical Trials Group. Li A, et al. Among authors: faruq mo. Crit Care. 2024 Jan 23;28(1):30. doi: 10.1186/s13054-024-04804-7. Crit Care. 2024. PMID: 38263076 Free PMC article.
Genetics of 67 patients of suspected primary ciliary dyskinesia from India.
Jat KR, Faruq M, Jindal S, Bari S, Soni A, Sharma P, Mathews S, Shamim U, Ahuja V, Uppilli B, Yadav SC, Lodha R, Arava SK, Kabra SK. Jat KR, et al. Among authors: faruq m. Clin Genet. 2024 Nov;106(5):650-658. doi: 10.1111/cge.14590. Epub 2024 Jul 14. Clin Genet. 2024. PMID: 39004944
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.
Molecular clues unveiling spinocerebellar ataxia type-12 pathogenesis.
Kumar M, Sahni S, A V, Kumar D, Kushwah N, Goel D, Kapoor H, Srivastava AK, Faruq M. Kumar M, et al. Among authors: faruq m. iScience. 2024 Apr 18;27(5):109768. doi: 10.1016/j.isci.2024.109768. eCollection 2024 May 17. iScience. 2024. PMID: 38711441 Free PMC article.
Allgrove Syndrome: A Frequently Under-Diagnosed ALS Mimic.
Agarwal A, Das A, Pandit AK, Radhakrishnan DM, Rajan R, Faruq M, Srivastava AK. Agarwal A, et al. Among authors: faruq m. Ann Indian Acad Neurol. 2022 May-Jun;25(3):500-501. doi: 10.4103/aian.aian_594_21. Epub 2021 Oct 22. Ann Indian Acad Neurol. 2022. PMID: 35936640 Free PMC article. No abstract available.
Synthetic transcription elongation factors license transcription across repressive chromatin.
Erwin GS, Grieshop MP, Ali A, Qi J, Lawlor M, Kumar D, Ahmad I, McNally A, Teider N, Worringer K, Sivasankaran R, Syed DN, Eguchi A, Ashraf M, Jeffery J, Xu M, Park PMC, Mukhtar H, Srivastava AK, Faruq M, Bradner JE, Ansari AZ. Erwin GS, et al. Among authors: faruq m. Science. 2017 Dec 22;358(6370):1617-1622. doi: 10.1126/science.aan6414. Epub 2017 Nov 30. Science. 2017. PMID: 29192133 Free PMC article.
168 results