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Biallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy.
Calame DG, Fatih J, Herman I, Akdemir ZC, Du H, Jhangiani SN, Gibbs RA, Marafi D, Pehlivan D, Posey JE, Lotze T, Mancias P, Bhattacharjee MB, Lupski JR. Calame DG, et al. Among authors: bhattacharjee mb. Neurol Genet. 2021 Apr 26;7(3):e589. doi: 10.1212/NXG.0000000000000589. eCollection 2021 Jun. Neurol Genet. 2021. PMID: 33977145 Free PMC article.
Treatment-resistant eosinophilic polymyositis in a child.
Mancias P, Bohan TP, Butler IJ, Bhattacharjee MB. Mancias P, et al. Among authors: bhattacharjee mb. J Child Neurol. 1994 Oct;9(4):446-8. doi: 10.1177/088307389400900425. J Child Neurol. 1994. PMID: 7822742 No abstract available.
Somatic variants in diverse genes leads to a spectrum of focal cortical malformations.
Lai D, Gade M, Yang E, Koh HY, Lu J, Walley NM, Buckley AF, Sands TT, Akman CI, Mikati MA, McKhann GM, Goldman JE, Canoll P, Alexander AL, Park KL, Von Allmen GK, Rodziyevska O, Bhattacharjee MB, Lidov HGW, Vogel H, Grant GA, Porter BE, Poduri AH, Crino PB, Heinzen EL. Lai D, et al. Among authors: bhattacharjee mb. Brain. 2022 Aug 27;145(8):2704-2720. doi: 10.1093/brain/awac117. Brain. 2022. PMID: 35441233 Free PMC article.
Molecular Alterations in Meningioangiomatosis Causing Epilepsy.
Dono A, Pothiawala AZ, Lewis CT, Bhattacharjee MB, Ballester LY, Tandon N. Dono A, et al. Among authors: bhattacharjee mb. J Neuropathol Exp Neurol. 2021 Nov 19;80(11):1043–1051. doi: 10.1093/jnen/nlab095. Epub 2021 Sep 27. J Neuropathol Exp Neurol. 2021. PMID: 34580720 Free PMC article.
91 results