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Journal Abstract Search

339 related items for PubMed ID: 31093799

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  • 46. CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathy.
    Mitsui J, Matsukawa T, Ishiura H, Higasa K, Yoshimura J, Saito TL, Ahsan B, Takahashi Y, Goto J, Iwata A, Niimi Y, Riku Y, Goto Y, Mano K, Yoshida M, Morishita S, Tsuji S.
    Am J Med Genet B Neuropsychiatr Genet; 2012 Dec; 159B(8):951-7. PubMed ID: 23038421
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  • 48. A novel A792D mutation in the CSF1R gene causes hereditary diffuse leukoencephalopathy with axonal spheroids characterized by slow progression.
    Ueda S, Yamashita H, Hikiami R, Sawamoto N, Yoshida K, Takahashi R.
    eNeurologicalSci; 2015 Mar; 1(1):7-9. PubMed ID: 29479570
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  • 51. Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia by a novel mutation of the CSF1R gene.
    Ding C, Zhao L, Zhan Y, Li J, Zhong R, Song Q, Dong C.
    Neurol Sci; 2022 Nov; 43(11):6433-6440. PubMed ID: 35971044
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  • 53. CSF1R mutations link POLD and HDLS as a single disease entity.
    Nicholson AM, Baker MC, Finch NA, Rutherford NJ, Wider C, Graff-Radford NR, Nelson PT, Clark HB, Wszolek ZK, Dickson DW, Knopman DS, Rademakers R.
    Neurology; 2013 Mar 12; 80(11):1033-40. PubMed ID: 23408870
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  • 55. Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features.
    Kındış E, Simsek-Kiper PÖ, Koşukcu C, Taşkıran EZ, Göçmen R, Utine E, Haliloğlu G, Boduroğlu K, Alikaşifoğlu M.
    Am J Med Genet A; 2021 Jun 12; 185(6):1888-1896. PubMed ID: 33749994
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  • 56. A case of CSF1R-related leukoencephalopathy: serial neuroimaging and neuropsychological tests.
    Sohn EH, Lee J, Lee AY, Shin JH.
    Neurocase; 2021 Oct 12; 27(5):415-418. PubMed ID: 34633276
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  • 58. CSF1R-related leukoencephalopathy: A major player in primary microgliopathies.
    Konno T, Kasanuki K, Ikeuchi T, Dickson DW, Wszolek ZK.
    Neurology; 2018 Dec 11; 91(24):1092-1104. PubMed ID: 30429277
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  • 60. A Novel Splicing Mutation in the CSF1R Gene in a Family With Hereditary Diffuse Leukoencephalopathy With Axonal Spheroids.
    Yang X, Huang P, Tan Y, Xiao Q.
    Front Genet; 2019 Dec 11; 10():491. PubMed ID: 31191609
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