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 *

162 related articles for article (PubMed ID: 36943150)

  • 1. Novel partial deletions, frameshift and missense mutations of CSF1R in patents with CSF1R-related leukoencephalopathy.
    Ishiguro T; Konno T; Hara N; Zhu B; Okada S; Shibata M; Saika R; Kitano T; Toko M; Nezu T; Hama Y; Kawazoe T; Takahashi-Iwata I; Yabe I; Sato K; Takeda H; Toda S; Nishimiya J; Teduka T; Nozaki H; Kasuga K; Miyashita A; Onodera O; Ikeuchi T
    Eur J Neurol; 2023 Jul; 30(7):1861-1870. PubMed ID: 36943150
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Four Swedish cases of CSF1R-related leukoencephalopathy: Visualization of clinical phenotypes.
    Rosenstein I; Andersen O; Victor D; Englund E; Granberg T; Hedberg-Oldfors C; Jood K; Fitrah YA; Ikeuchi T; Danylaité Karrenbauer V
    Acta Neurol Scand; 2022 May; 145(5):599-609. PubMed ID: 35119108
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Evaluation of CSF1R-related adult onset leukoencephalopathy with axonal spheroids and pigmented glia diagnostic criteria.
    Ayrignac X; Carra-Dallière C; Codjia P; Mouzat K; Castelnovo G; Ellie E; Etcharry-Bouyx F; Belliard S; Marelli C; Portet F; Le Ber I; Durand-Dubief F; Mathey G; Stankoff B; Dorboz I; Drunat S; Boespflug-Tanguy O; Menjot de Champfleur N; Lumbroso S; Mochel F; Labauge P
    Eur J Neurol; 2022 Jan; 29(1):329-334. PubMed ID: 34541732
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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; 271(9):6025-6037. PubMed ID: 39031193
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    Konno T; Kasanuki K; Ikeuchi T; Dickson DW; Wszolek ZK
    Neurology; 2018 Dec; 91(24):1092-1104. PubMed ID: 30429277
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Neuroimaging phenotypes of CSF1R-related leukoencephalopathy: Systematic review, meta-analysis, and imaging recommendations.
    Mickeviciute GC; Valiuskyte M; Plattén M; Wszolek ZK; Andersen O; Danylaité Karrenbauer V; Ineichen BV; Granberg T
    J Intern Med; 2022 Mar; 291(3):269-282. PubMed ID: 34875121
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Factors predictive of the presence of a CSF1R mutation in patients with leukoencephalopathy.
    Kondo Y; Matsushima A; Nagasaki S; Nakamura K; Sekijima Y; Yoshida K
    Eur J Neurol; 2020 Feb; 27(2):369-375. PubMed ID: 31520500
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of Microglia.
    Oosterhof N; Chang IJ; Karimiani EG; Kuil LE; Jensen DM; Daza R; Young E; Astle L; van der Linde HC; Shivaram GM; Demmers J; Latimer CS; Keene CD; Loter E; Maroofian R; van Ham TJ; Hevner RF; Bennett JT
    Am J Hum Genet; 2019 May; 104(5):936-947. PubMed ID: 30982608
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.