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Page 1
Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease.
Cogal AG, Arroyo J, Shah RJ, Reese KJ, Walton BN, Reynolds LM, Kennedy GN, Seide BM, Senum SR, Baum M, Erickson SB, Jagadeesh S, Soliman NA, Goldfarb DS, Beara-Lasic L, Edvardsson VO, Palsson R, Milliner DS, Sas DJ, Lieske JC, Harris PC; Investigators of the Rare Kidney Stone Consortium. Cogal AG, et al. Among authors: jagadeesh s. Kidney Int Rep. 2021 Sep 8;6(11):2862-2884. doi: 10.1016/j.ekir.2021.08.033. eCollection 2021 Nov. Kidney Int Rep. 2021. PMID: 34805638 Free PMC article.
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies.
Lischka A, Eggermann K, Record CJ, Dohrn MF, Laššuthová P, Kraft F, Begemann M, Dey D, Eggermann T, Beijer D, Šoukalová J, Laura M, Rossor AM, Mazanec R, Van Lent J, Tomaselli PJ, Ungelenk M, Debus KY, Feely SME, Gläser D, Jagadeesh S, Martin M, Govindaraj GM, Singhi P, Baineni R, Biswal N, Ibarra-Ramírez M, Bonduelle M, Gess B, Romero Sánchez J, Suthar R, Udani V, Nalini A, Unnikrishnan G, Marques W Junior, Mercier S, Procaccio V, Bris C, Suresh B, Reddy V, Skorupinska M, Bonello-Palot N, Mochel F, Dahl G, Sasidharan K, Devassikutty FM, Nampoothiri S, Rodovalho Doriqui MJ, Müller-Felber W, Vill K, Haack TB, Dufke A, Abele M, Stucka R, Siddiqi S, Ullah N, Spranger S, Chiabrando D, Bolgül BS, Parman Y, Seeman P, Lampert A, Schulz JB, Wood JN, Cox JJ, Auer-Grumbach M, Timmerman V, de Winter J, Themistocleous AC, Shy M, Bennett DL, Baets J, Hübner CA, Leipold E, Züchner S, Elbracht M, Çakar A, Senderek J, Hornemann T, Woods CG, Reilly MM, Kurth I. Lischka A, et al. Among authors: jagadeesh s. Brain. 2023 Dec 1;146(12):4880-4890. doi: 10.1093/brain/awad328. Brain. 2023. PMID: 37769650 Free PMC article.
Fanconi-Bickel syndrome.
Mohandas Nair K, Sakamoto O, Jagadeesh S, Nampoothiri S. Mohandas Nair K, et al. Among authors: jagadeesh s. Indian J Pediatr. 2012 Jan;79(1):112-4. doi: 10.1007/s12098-011-0373-5. Epub 2011 Feb 15. Indian J Pediatr. 2012. PMID: 21327337
Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.
Yadav RM, Gupta M, Dalvi A, Bargir UA, Hule G, Shabrish S, Aluri J, Kulkarni M, Kambli P, Uppuluri R, Seshadri S, Jagadeesh S, Suresh B, Raja J, Taur P, Malaischamy S, Ghosh P, Mahalingam S, Kadam P, Lashkari HP, Tamhankar P, Tamhankar V, Mithbawkar S, Bhattad S, Jhawar P, Makam A, Bansal V, Prasad M, Govindaraj G, Guhan B, Bharadwaj Tallapaka K, Desai M, Raj R, Madkaikar MR. Yadav RM, et al. Among authors: jagadeesh s. Front Immunol. 2020 Dec 7;11:612316. doi: 10.3389/fimmu.2020.612316. eCollection 2020. Front Immunol. 2020. PMID: 33365035 Free PMC article. Review.
Receptor tyrosine kinases and inhibitors in lung cancer.
Pisick E, Jagadeesh S, Salgia R. Pisick E, et al. Among authors: jagadeesh s. ScientificWorldJournal. 2004 Aug 6;4:589-604. doi: 10.1100/tsw.2004.117. ScientificWorldJournal. 2004. PMID: 15349502 Free PMC article. Review.
Natural History of Vanishing White Matter.
Hamilton EMC, van der Lei HDW, Vermeulen G, Gerver JAM, Lourenço CM, Naidu S, Mierzewska H, Gemke RJBJ, de Vet HCW, Uitdehaag BMJ, Lissenberg-Witte BI; VWM Research Group; van der Knaap MS. Hamilton EMC, et al. Ann Neurol. 2018 Aug;84(2):274-288. doi: 10.1002/ana.25287. Epub 2018 Sep 6. Ann Neurol. 2018. PMID: 30014503 Free PMC article.
Uveal Effusion Syndrome Due to WNT10A Mutation.
Patnaik G, Jagadeesh S, Bhende M, Biswas J. Patnaik G, et al. Among authors: jagadeesh s. Ocul Immunol Inflamm. 2024 Oct 15:1-5. doi: 10.1080/09273948.2024.2413903. Online ahead of print. Ocul Immunol Inflamm. 2024. PMID: 39405081
90 results