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 *

215 related articles for article (PubMed ID: 24532199)

  • 21. 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; 80(11):1033-40. PubMed ID: 23408870
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel mutation in the CSF1R gene causes a variable leukoencephalopathy with spheroids.
    La Piana R; Webber A; Guiot MC; Del Pilar Cortes M; Brais B
    Neurogenetics; 2014 Oct; 15(4):289-94. PubMed ID: 25012610
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hereditary diffuse leukoencephalopathy with spheroids - a volumetric and radiological comparison with multiple sclerosis patients and healthy controls.
    Granberg T; Hashim F; Andersen O; Sundal C; Karrenbauer VD
    Eur J Neurol; 2016 Apr; 23(4):817-22. PubMed ID: 26756564
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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; 185(6):1888-1896. PubMed ID: 33749994
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. From HDLS to BANDDOS: fast-expanding phenotypic spectrum of disorders caused by mutations in CSF1R.
    Guo L; Ikegawa S
    J Hum Genet; 2021 Dec; 66(12):1139-1144. PubMed ID: 34135456
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia Caused by a Novel R782G Mutation in CSF1R.
    Foulds N; Pengelly RJ; Hammans SR; Nicoll JA; Ellison DW; Ditchfield A; Beck S; Ennis S
    Sci Rep; 2015 May; 5():10042. PubMed ID: 25975230
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Characterization of spheroids in hereditary diffuse leukoencephalopathy with axonal spheroids.
    Jin C; Washimi Y; Yoshida K; Hashizume Y; Yazawa I
    J Neurol Sci; 2015 May; 352(1-2):74-8. PubMed ID: 25843289
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. [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]  

  • 32. 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]  

  • 33. 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]  

  • 34. Adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia: report of five cases and a new mutation.
    Kleinfeld K; Mobley B; Hedera P; Wegner A; Sriram S; Pawate S
    J Neurol; 2013 Feb; 260(2):558-71. PubMed ID: 23052599
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis.
    Sundal C; Baker M; Karrenbauer V; Gustavsen M; Bedri S; Glaser A; Myhr KM; Haugarvoll K; Zetterberg H; Harbo H; Kockum I; Hillert J; Wszolek Z; Rademakers R; Andersen O
    Eur J Neurol; 2015 Feb; 22(2):328-333. PubMed ID: 25311247
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Clinical and genetic characterization of adult-onset leukoencephalopathy caused by CSF1R mutations.
    Tsai PC; Fuh JL; Yang CC; Chang A; Lien LM; Wang PN; Lai KL; Tsai YS; Lee YC; Liao YC
    Ann Clin Transl Neurol; 2021 Nov; 8(11):2121-2131. PubMed ID: 34652888
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Analysis of CSF1R gene mutation in a Chinese family with hereditary diffuse leukoencephalopathy with neuroaxonal spheroids].
    Cheng X; Shen W; Zou H; Shen L; Gu X; Huang D; Sun Y; Wang B; Tian Q; Xu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):208-12. PubMed ID: 25863088
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.