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 *

369 related articles for article (PubMed ID: 27190017)

  • 21. Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation.
    Konno T; Yoshida K; Mizuta I; Mizuno T; Kawarai T; Tada M; Nozaki H; Ikeda SI; Onodera O; Wszolek ZK; Ikeuchi T
    Eur J Neurol; 2018 Jan; 25(1):142-147. PubMed ID: 28921817
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Early involvement of the corpus callosum in a patient with hereditary diffuse leukoencephalopathy with spheroids carrying the de novo K793T mutation of CSF1R.
    Kondo Y; Kinoshita M; Fukushima K; Yoshida K; Ikeda S
    Intern Med; 2013; 52(4):503-6. PubMed ID: 23411710
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Neuropathology of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS)].
    Oyanagi K
    Rinsho Shinkeigaku; 2014; 54(12):1165-7. PubMed ID: 25672734
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Increasing and persistent DWI changes in a patient with hereditary diffuse leukoencephalopathy with spheroids.
    Terasawa Y; Osaki Y; Kawarai T; Sugimoto T; Orlacchio A; Abe T; Izumi Y; Kaji R
    J Neurol Sci; 2013 Dec; 335(1-2):213-5. PubMed ID: 24094860
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 10():491. PubMed ID: 31191609
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene.
    Battisti C; Di Donato I; Bianchi S; Monti L; Formichi P; Rufa A; Taglia I; Cerase A; Dotti MT; Federico A
    J Neurol; 2014 Apr; 261(4):768-72. PubMed ID: 24532199
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalities.
    Konno T; Miura T; Harriott AM; Mezaki N; Edwards ES; Rademakers R; Ross OA; Meschia JF; Ikeuchi T; Wszolek ZK
    Eur J Neurol; 2018 Jun; 25(6):875-881. PubMed ID: 29509319
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroids.
    Ahmed R; Guerreiro R; Rohrer JD; Guven G; Rossor MN; Hardy J; Fox NC
    J Neurol Sci; 2013 Sep; 332(1-2):141-4. PubMed ID: 23816250
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A new CSF1R mutation presenting with an extensive white matter lesion mimicking primary progressive multiple sclerosis.
    Inui T; Kawarai T; Fujita K; Kawamura K; Mitsui T; Orlacchio A; Kamada M; Abe T; Izumi Y; Kaji R
    J Neurol Sci; 2013 Nov; 334(1-2):192-5. PubMed ID: 24034409
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. A case of
    Sohn EH; Lee J; Lee AY; Shin JH
    Neurocase; 2021 Oct; 27(5):415-418. PubMed ID: 34633276
    [TBL] [Abstract][Full Text] [Related]  

  • 32. AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases.
    Taglia I; Di Donato I; Bianchi S; Cerase A; Monti L; Marconi R; Orrico A; Rufa A; Federico A; Dotti MT
    Acta Neurol Scand; 2018 Oct; 138(4):278-283. PubMed ID: 29749055
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel CSF-1R mutation in a family with hereditary diffuse leukoencephalopathy with axonal spheroids misdiagnosed as hydrocephalus.
    Wang M; Zhang X
    Neurogenetics; 2019 Aug; 20(3):155-160. PubMed ID: 31093799
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Early pathologic changes in hereditary diffuse leukoencephalopathy with spheroids.
    Riku Y; Ando T; Goto Y; Mano K; Iwasaki Y; Sobue G; Yoshida M
    J Neuropathol Exp Neurol; 2014 Dec; 73(12):1183-90. PubMed ID: 25383640
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Enlarging the nosological spectrum of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS).
    Hoffmann S; Murrell J; Harms L; Miller K; Meisel A; Brosch T; Scheel M; Ghetti B; Goebel HH; Stenzel W
    Brain Pathol; 2014 Sep; 24(5):452-8. PubMed ID: 24428556
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hereditary diffuse leukoencephalopathy with spheroids mimicking primary progressive aphasia: report of a Greek case.
    Stoiloudis P; Parissis D; Smyrni N; Stardeli T; Afrantou T; Konstantinopoulou E; Grigoriadis N; Ioannidis P
    Neurol Sci; 2021 Aug; 42(8):3431-3433. PubMed ID: 33866445
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS).
    Karle KN; Biskup S; Schüle R; Schweitzer KJ; Krüger R; Bauer P; Bender B; Nägele T; Schöls L
    Neurology; 2013 Dec; 81(23):2039-44. PubMed ID: 24198292
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of a de novo splicing mutation in the CSF1R gene in a Chinese patient with hereditary diffuse leukoencephalopathy with spheroids.
    Wu X; Sun C; Wang X; Liu Y; Wu W; Jia G
    Neurol Sci; 2022 May; 43(5):3265-3272. PubMed ID: 34791569
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification and functional characterization of novel mutations including frameshift mutation in exon 4 of CSF1R in patients with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia.
    Miura T; Mezaki N; Konno T; Iwasaki A; Hara N; Miura M; Funayama M; Unai Y; Tashiro Y; Okita K; Kihara T; Ito N; Kanatsuka Y; Jones DT; Hara N; Ishiguro T; Tokutake T; Kasuga K; Nozaki H; Dickson DW; Onodera O; Wszolek ZK; Ikeuchi T
    J Neurol; 2018 Oct; 265(10):2415-2424. PubMed ID: 30136118
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.