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 *

185 related articles for article (PubMed ID: 32220229)

  • 1. The disappearance of white matter in an adult-onset disease: a case report.
    Ho CS; Mangelsdorf S; Walterfang M
    BMC Psychiatry; 2020 Mar; 20(1):137. PubMed ID: 32220229
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Adult-onset vanishing white matter disease with the EIF2B2 gene mutation presenting as menometrorrhagia.
    Wei C; Qin Q; Chen F; Zhou A; Wang F; Zuo X; Chen R; Lyu J; Jia J
    BMC Neurol; 2019 Aug; 19(1):203. PubMed ID: 31438897
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Vanishing white matter disease presenting as opsoclonus myoclonus syndrome in childhood--a case report and review of the literature.
    Klingelhoefer L; Misbahuddin A; Jawad T; Mellers J; Jarosz J; Weeks R; Ray Chaudhuri K
    Pediatr Neurol; 2014 Jul; 51(1):157-64. PubMed ID: 24938145
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Juxtacortical White Matter Hypointensity on T2*Gradient Echo Image in Vanishing White Matter Disease: A Case Report.
    Lim CG; Hahm MH; Lee HJ
    Am J Case Rep; 2023 Feb; 24():e938569. PubMed ID: 36793200
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An eleven-year history of Vanishing White Matter Disease in an adult patient with no cognitive decline and
    Trevisan L; Grazzini M; Cianflone A; Accogli A; Finocchi C; Capello E; Saitta L; Grandis M; Roccatagliata L; Mandich P
    Neurocase; 2021 Dec; 27(6):452-456. PubMed ID: 34751098
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Adult Vanishing White Matter Disease with a Novel EIF2B4 Mutation.
    Su T; Yuan H; Gao W; Li H; Yuan M
    J Coll Physicians Surg Pak; 2022 Dec; 32(12):SS181-SS183. PubMed ID: 36597332
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Adult-onset leukoencephalopathy with vanishing white matter with compound heterozygous EIF2B3 gene variants.
    Gui M; He M; Qin L
    BMC Neurol; 2024 Jun; 24(1):201. PubMed ID: 38872124
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. An unusual neuroimaging finding and response to immunotherapy in a child with genetically confirmed vanishing white matter disease.
    Singh RR; Livingston J; Lim M; Berry IR; Siddiqui A
    Eur J Paediatr Neurol; 2017 Mar; 21(2):410-413. PubMed ID: 27665184
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Brain magnetic resonance imaging helps to differentiate atypical multiple sclerosis with cavitary lesions and vanishing white matter disease.
    Ayrignac X; Menjot de Champfleur N; Menjot de Champfleur S; Carra-Dallière C; Deverdun J; Corlobe A; Labauge P
    Eur J Neurol; 2016 Jun; 23(6):995-1000. PubMed ID: 26727496
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Adult Onset Vanishing White Matter Disease: A Rare Case Report.
    Nagdev G; Vhora RS; Chavan G; Sahu G
    Cureus; 2022 Oct; 14(10):e30177. PubMed ID: 36397907
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Case of adult onset vanishing white matter disease developed after minor head trauma].
    Koga S; Sekiguchi Y; Kanai K; Mutoh M; Kuwabara S
    Rinsho Shinkeigaku; 2012; 52(8):561-6. PubMed ID: 22975854
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Vanishing white matter disease, a rare leukodystrophy with mutation in the EIF2B5 gene].
    Sinkó G; Tompa M; Kiss Z; Kálmán B
    Ideggyogy Sz; 2024 May; 77(5-6):207-211. PubMed ID: 38829246
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inherited leukoencephalopathies with clinical onset in middle and old age.
    Nannucci S; Donnini I; Pantoni L
    J Neurol Sci; 2014 Dec; 347(1-2):1-13. PubMed ID: 25307983
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Uncertainty of leukoencephalopathies: a case report.
    Taha MA; Diesing TS
    J Med Case Rep; 2021 Nov; 15(1):561. PubMed ID: 34784967
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distinctive diffusion-weighted imaging features in late-onset genetic leukoencephalopathies.
    De Cocker LJL; Castillo M
    Neuroradiology; 2021 Jan; 63(1):153-156. PubMed ID: 32879996
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Edaravone and mitochondrial transfer as potential therapeutics for vanishing white matter disease astrocyte dysfunction.
    Ng NS; Newbery M; Touffu A; Maksour S; Chung J; Carroll L; Zaw T; Wu Y; Ooi L
    CNS Neurosci Ther; 2023 Sep; 29(9):2481-2497. PubMed ID: 36971196
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New Insights in Vanishing White Matter Disease: Isolated Bilateral Optic Neuropathy in Adult Onset Disease.
    Barros SR; Parreira SCR; Miranda AFB; Pereira AMB; Campos NMP
    J Neuroophthalmol; 2018 Mar; 38(1):42-46. PubMed ID: 28902089
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?
    Bindu PS; Sonam K; Chiplunkar S; Govindaraj P; Nagappa M; Vekhande CC; Aravinda HR; Ponmalar JJ; Mahadevan A; Gayathri N; Bharath MS; Sinha S; Taly AB
    Mult Scler Relat Disord; 2018 Feb; 20():84-92. PubMed ID: 29353736
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Vanishing white matter disease caused by EIF2B2 mutation with the presentation of an adrenoleukodystrophy phenotype.
    Alsalem A; Shaheen R; Alkuraya FS
    Gene; 2012 Apr; 496(2):141-3. PubMed ID: 22285377
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.