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Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome.
Govindaraj GM, Jain A, Peethambaran G, Bhoyar RC, Vellarikkal SK, Ganapati A, Sandhya P, Edavazhippurath A, Dhanasooraj D, Puthenpurayil JM, Chakkiyar K, Mishra A, Batra A, Punnen A, Kumar S, Sivasubbu S, Scaria V. Govindaraj GM, et al. Among authors: kumar s. PLoS One. 2020 Aug 21;15(8):e0237999. doi: 10.1371/journal.pone.0237999. eCollection 2020. PLoS One. 2020. PMID: 32822427 Free PMC article.
Neonate with orbital bleed.
Punnen A, Loganathan SK, Veetiyil GI, Scott JX, Kumar S. Punnen A, et al. Among authors: kumar s. Pediatr Blood Cancer. 2015 Mar;62(3):548. doi: 10.1002/pbc.25339. Epub 2014 Nov 28. Pediatr Blood Cancer. 2015. PMID: 25447027 No abstract available.
Tale of a chest radiograph in Takayasu's arteritis.
Punnen AK, Sudhakar M, Kumar S. Punnen AK, et al. Among authors: kumar s. Arch Dis Child. 2024 Feb 19;109(3):247. doi: 10.1136/archdischild-2023-326334. Arch Dis Child. 2024. PMID: 38041676 No abstract available.
Clinical spectrum and outcome of children with deficiency of adenosine deaminase 2 (DADA2): multicentric experience from India.
Kumar S, Chugh A, Kumar SC, Punnen A, Bhat C, Patra P, Viswanathan V, Gupta A, Aggarwal M, Nayak AR, Lingappa L, Sharma J, Gupta N, Naranje P, Jana M, Bagri NK, Hari P, Ramanan AV. Kumar S, et al. Among authors: kumar sc. Rheumatology (Oxford). 2024 Sep 11:keae489. doi: 10.1093/rheumatology/keae489. Online ahead of print. Rheumatology (Oxford). 2024. PMID: 39259214
31,987 results
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