These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

324 related articles for article (PubMed ID: 23698128)

  • 41. [Clinical and neuroimaging characteristics of patients with hereditary diffuse leukoencephalopathy with spheroids (HDLS)].
    Ikeuchi T
    Rinsho Shinkeigaku; 2014; 54(12):1158-61. PubMed ID: 25519969
    [TBL] [Abstract][Full Text] [Related]  

  • 42. CSF1R mutations in hereditary diffuse leukoencephalopathy with spheroids are loss of function.
    Pridans C; Sauter KA; Baer K; Kissel H; Hume DA
    Sci Rep; 2013 Oct; 3():3013. PubMed ID: 24145216
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): Integrating the literature on hereditary diffuse leukoencephalopathy with spheroids (HDLS) and pigmentary orthochromatic leukodystrophy (POLD).
    Adams SJ; Kirk A; Auer RN
    J Clin Neurosci; 2018 Feb; 48():42-49. PubMed ID: 29122458
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids.
    Rademakers R; Baker M; Nicholson AM; Rutherford NJ; Finch N; Soto-Ortolaza A; Lash J; Wider C; Wojtas A; DeJesus-Hernandez M; Adamson J; Kouri N; Sundal C; Shuster EA; Aasly J; MacKenzie J; Roeber S; Kretzschmar HA; Boeve BF; Knopman DS; Petersen RC; Cairns NJ; Ghetti B; Spina S; Garbern J; Tselis AC; Uitti R; Das P; Van Gerpen JA; Meschia JF; Levy S; Broderick DF; Graff-Radford N; Ross OA; Miller BB; Swerdlow RH; Dickson DW; Wszolek ZK
    Nat Genet; 2011 Dec; 44(2):200-5. PubMed ID: 22197934
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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; 24(1):37-45. PubMed ID: 27680516
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Adult-onset vanishing white matter disease as differential diagnosis of primary progressive multiple sclerosis: a case report.
    Herwerth M; Schwaiger BJ; Kreiser K; Hemmer B; Ilg R
    Mult Scler; 2015 Apr; 21(5):666-8. PubMed ID: 25135182
    [TBL] [Abstract][Full Text] [Related]  

  • 47. MRI characteristics and scoring in HDLS due to CSF1R gene mutations.
    Sundal C; Van Gerpen JA; Nicholson AM; Wider C; Shuster EA; Aasly J; Spina S; Ghetti B; Roeber S; Garbern J; Borjesson-Hanson A; Tselis A; Swerdlow RH; Miller BB; Fujioka S; Heckman MG; Uitti RJ; Josephs KA; Baker M; Andersen O; Rademakers R; Dickson DW; Broderick D; Wszolek ZK
    Neurology; 2012 Aug; 79(6):566-74. PubMed ID: 22843259
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Recent advances of study on hereditary diffuse leukoencephalopathy with spheroids].
    Cheng X; Xu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):330-3. PubMed ID: 24928013
    [TBL] [Abstract][Full Text] [Related]  

  • 49. AARS2 Compound Heterozygous Variants in a Case of Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia.
    Wang D; Yu M; Zhang W; Wang Z; Yuan Y
    J Neuropathol Exp Neurol; 2018 Nov; 77(11):997-1000. PubMed ID: 30272204
    [TBL] [Abstract][Full Text] [Related]  

  • 50. MR Spectroscopy in Patients with Hereditary Diffuse Leukoencephalopathy with Spheroids and Asymptomatic Carriers of Colony-stimulating Factor 1 Receptor Mutation.
    Abe T; Kawarai T; Fujita K; Sako W; Terasawa Y; Matsuda T; Sakai W; Tsukamoto-Miyashiro A; Matsui N; Izumi Y; Kaji R; Harada M
    Magn Reson Med Sci; 2017 Oct; 16(4):297-303. PubMed ID: 28025469
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Comprehensive diagnostics in a case of hereditary diffuse leukodystrophy with spheroids.
    Meyer-Ohlendorf M; Braczynski A; Al-Qaisi O; Gessler F; Biskup S; Weise L; Steinbach JP; Wagner M; Mittelbronn M; Bähr O
    BMC Neurol; 2015 Jul; 15():103. PubMed ID: 26141177
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A novel mutation in the CSF1R gene causes hereditary diffuse leukoencephalopathy with axonal spheroids.
    Du Q; Chen H; Shi Z; Zhang Y; Wang J; Zhou H
    Neurol Sci; 2019 Jun; 40(6):1287-1290. PubMed ID: 30617447
    [No Abstract]   [Full Text] [Related]  

  • 53. Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene.
    Guerreiro R; Kara E; Le Ber I; Bras J; Rohrer JD; Taipa R; Lashley T; Dupuits C; Gurunlian N; Mochel F; Warren JD; Hannequin D; Sedel F; Depienne C; Camuzat A; Golfier V; Du Boisguéheneuc F; Schottlaender L; Fox NC; Beck J; Mead S; Rossor MN; Hardy J; Revesz T; Brice A; Houlden H
    JAMA Neurol; 2013 Jul; 70(7):875-882. PubMed ID: 23649896
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A young-onset frontal dementia with dramatic calcifications due to a novel CSF1R mutation.
    Gore E; Manley A; Dees D; Appleby BS; Lerner AJ
    Neurocase; 2016 Jun; 22(3):257-62. PubMed ID: 27092868
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Sporadic Cases with Novel Mutations and Pedigree in Hereditary Leukoencephalopathy with Axonal Spheroids.
    Wu L; Liu J; Sha L; Wang X; Li J; Dong J; Jia J
    J Alzheimers Dis; 2017; 56(3):893-898. PubMed ID: 28059798
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Dynamic analysis of CSF1R-related leukoencephalopathy on magnetic resonance imaging: a case report.
    Huang H; Cao L; Chen H
    BMC Neurol; 2021 Apr; 21(1):156. PubMed ID: 33838643
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Novel
    Arshad F; Vengalil S; Maskomani S; Kamath SD; Kulanthaivelu K; Mundlamuri RC; Yadav R; Nalini A
    Neurocase; 2021 Dec; 27(6):484-489. PubMed ID: 34983323
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Analysis of Mutations in AARS2 in a Series of CSF1R-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia.
    Lynch DS; Zhang WJ; Lakshmanan R; Kinsella JA; Uzun GA; Karbay M; Tüfekçioglu Z; Hanagasi H; Burke G; Foulds N; Hammans SR; Bhattacharjee A; Wilson H; Adams M; Walker M; Nicoll JA; Chataway J; Fox N; Davagnanam I; Phadke R; Houlden H
    JAMA Neurol; 2016 Dec; 73(12):1433-1439. PubMed ID: 27749956
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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; 8(1):72. PubMed ID: 32430064
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.