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Journal Abstract Search
403 related items for PubMed ID: 33287883
1. Microglial replacement therapy: a potential therapeutic strategy for incurable CSF1R-related leukoencephalopathy. Han J, Sarlus H, Wszolek ZK, Karrenbauer VD, Harris RA. Acta Neuropathol Commun; 2020 Dec 07; 8(1):217. PubMed ID: 33287883 [Abstract] [Full Text] [Related]
12. Loss of homeostatic microglial phenotype in CSF1R-related Leukoencephalopathy. Kempthorne L, Yoon H, Madore C, Smith S, Wszolek ZK, Rademakers R, Kim J, Butovsky O, Dickson DW. Acta Neuropathol Commun; 2020 May 19; 8(1):72. PubMed ID: 32430064 [Abstract] [Full Text] [Related]
13. Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation. Konno T, Yoshida K, Mizuno T, Kawarai T, Tada M, Nozaki H, Ikeda SI, Nishizawa M, Onodera O, Wszolek ZK, Ikeuchi T. Eur J Neurol; 2017 Jan 19; 24(1):37-45. PubMed ID: 27680516 [Abstract] [Full Text] [Related]
14. Therapeutic potential of human microglia transplantation in a chimeric model of CSF1R-related leukoencephalopathy. Chadarevian JP, Hasselmann J, Lahian A, Capocchi JK, Escobar A, Lim TE, Le L, Tu C, Nguyen J, Kiani Shabestari S, Carlen-Jones W, Gandhi S, Bu G, Hume DA, Pridans C, Wszolek ZK, Spitale RC, Davtyan H, Blurton-Jones M. Neuron; 2024 Aug 21; 112(16):2686-2707.e8. PubMed ID: 38897209 [Abstract] [Full Text] [Related]
15. Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophy. Berdowski WM, van der Linde HC, Breur M, Oosterhof N, Beerepoot S, Sanderson L, Wijnands LI, de Jong P, Tsai-Meu-Chong E, de Valk W, de Witte M, van IJcken WFJ, Demmers J, van der Knaap MS, Bugiani M, Wolf NI, van Ham TJ. Acta Neuropathol; 2022 Aug 21; 144(2):211-239. PubMed ID: 35713703 [Abstract] [Full Text] [Related]
16. Colony-Stimulating Factor 1 Receptor (CSF1R) Regulates Microglia Density and Distribution, but Not Microglia Differentiation In Vivo. Oosterhof N, Kuil LE, van der Linde HC, Burm SM, Berdowski W, van Ijcken WFJ, van Swieten JC, Hol EM, Verheijen MHG, van Ham TJ. Cell Rep; 2018 Jul 31; 24(5):1203-1217.e6. PubMed ID: 30067976 [Abstract] [Full Text] [Related]
17. Recent Advances in Basic Research for CSF1R-Microglial Encephalopathy. Wang YL, Wang FZ, Li R, Jiang J, Liu X, Xu J. Front Aging Neurosci; 2021 Jul 31; 13():792840. PubMed ID: 34955818 [Abstract] [Full Text] [Related]
18. A novel CSF1R variant in a South Dakota family with CSF1R-related leukoencephalopathy. Ali S, Tipton PW, Koga S, Middlebrooks EH, Josephs KA, Strongosky A, Dickson DW, Wszolek ZK. Parkinsonism Relat Disord; 2022 Sep 31; 102():51-53. PubMed ID: 35940158 [No Abstract] [Full Text] [Related]
19. Functional characterization of a novel CSF1R mutation causing hereditary diffuse leukoencephalopathy with spheroids. Kraya T, Quandt D, Pfirrmann T, Kindermann A, Lampe L, Schroeter ML, Kohlhase J, Stoevesandt D, Hoffmann K, Villavicencio-Lorini P. Mol Genet Genomic Med; 2019 Apr 31; 7(4):e00595. PubMed ID: 30729751 [Abstract] [Full Text] [Related]
20. Novel variants in CSF1R associated with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP). Schmitz AS, Raju J, Köhler W, Klebe S, Cheheb K, Reschke F, Biskup S, Haack TB, Roeben B, Kellner M, Rahner N, Bloch T, Lemke J, Bender B, Schöls L, Hengel H, Hayer SN. J Neurol; 2024 Sep 31; 271(9):6025-6037. PubMed ID: 39031193 [Abstract] [Full Text] [Related] Page: [Next] [New Search]