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: 31046592)

  • 1. Long-Standing Psychiatric Features as the Only Clinical Presentation of Vanishing White Matter Disease.
    Accogli A; Brais B; Tampieri D; La Piana R
    J Neuropsychiatry Clin Neurosci; 2019; 31(3):276-279. PubMed ID: 31046592
    [No Abstract]   [Full Text] [Related]  

  • 2. [Spasticity and progressive ataxia due to vanishing white matter].
    Paez-Granda D; Jimenez-Sanchez A; Fernandez-Hernandez C; Serrano-Garcia C
    Rev Neurol; 2017 Dec; 65(12):563-564. PubMed ID: 29235619
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Teaching NeuroImages: Vanishing white matter ovarioleukodystrophy.
    Mukerji SS; Eichler FS
    Neurology; 2016 Jun; 86(24):e248. PubMed ID: 27298454
    [No Abstract]   [Full Text] [Related]  

  • 5. Adult-onset vanishing white matter disease due to a novel EIF2B3 mutation.
    La Piana R; Vanderver A; van der Knaap M; Roux L; Tampieri D; Brais B; Bernard G
    Arch Neurol; 2012 Jun; 69(6):765-68. PubMed ID: 22312164
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease.
    Wu Y; Pan Y; Du L; Wang J; Gu Q; Gao Z; Li J; Leng X; Qin J; Wu X; Jiang Y
    J Hum Genet; 2009 Feb; 54(2):74-7. PubMed ID: 19158808
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Advances in functional study of EIF2B mutations in leukoencephalopathy with vanishing white matter].
    Leng XR; Wu Y; Jiang YW
    Sheng Li Ke Xue Jin Zhan; 2010 Apr; 41(2):125-8. PubMed ID: 21416999
    [No Abstract]   [Full Text] [Related]  

  • 8. Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease.
    Shimada S; Shimojima K; Sangu N; Hoshino A; Hachiya Y; Ohto T; Hashi Y; Nishida K; Mitani M; Kinjo S; Tsurusaki Y; Matsumoto N; Morimoto M; Yamamoto T
    Brain Dev; 2015 Nov; 37(10):960-6. PubMed ID: 25843247
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation.
    Ghezzi L; Scarpini E; Rango M; Arighi A; Bassi MT; Tenderini E; De Riz M; Jacini F; Fumagalli GG; Pietroboni AM; Galimberti D; Bresolin N
    Neurology; 2012 Nov; 79(20):2077-8. PubMed ID: 23115207
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Ovarioleukodystrophy due to EIF2B5 mutations.
    Ibitoye RT; Renowden SA; Faulkner HJ; Scolding NJ; Rice CM
    Pract Neurol; 2016 Dec; 16(6):496-499. PubMed ID: 27651498
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adult-onset leukoencephalopathies with vanishing white matter with novel missense mutations in EIF2B2, EIF2B3, and EIF2B5.
    Matsukawa T; Wang X; Liu R; Wortham NC; Onuki Y; Kubota A; Hida A; Kowa H; Fukuda Y; Ishiura H; Mitsui J; Takahashi Y; Aoki S; Takizawa S; Shimizu J; Goto J; Proud CG; Tsuji S
    Neurogenetics; 2011 Aug; 12(3):259-61. PubMed ID: 21484434
    [No Abstract]   [Full Text] [Related]  

  • 13. Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patients.
    Benzoni C; Moscatelli M; Farina L; Magri S; Ciano C; Scaioli V; Alverà S; Cammarata G; Bianchi-Marzoli S; Castellani M; Zito FM; Marotta G; Piacentini S; Villacara A; Mantegazza R; Gellera C; Durães J; Gouveia A; Matos A; do Carmo Macário M; Pareyson D; Taroni F; Di Bella D; Salsano E
    J Neurol; 2023 Sep; 270(9):4219-4234. PubMed ID: 37171481
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Leukoencephalopathy with vanishing white matter: a clinical case of adult onset].
    Pato Pato A; Lorenzo González JR; Cimas Hernando I; Rodríguez-Constenla I
    Neurologia; 2009 Sep; 24(7):504-5. PubMed ID: 21469262
    [No Abstract]   [Full Text] [Related]  

  • 15. Teaching NeuroImages: Adult-onset vanishing white matter disease.
    Villar-Quiles RN; Delgado-Suárez C; Jorquera-Moya M; Arpa-Gutiérrez J; Ortega-Suero G
    Neurology; 2018 Mar; 90(12):e1091-e1092. PubMed ID: 29555891
    [No Abstract]   [Full Text] [Related]  

  • 16. Leukodystrophy Due to
    Shivaram S; Nagappa M; Seshagiri DV; Saini J; Govindaraj P; Sinha S; Bindu PS; Taly AB
    Can J Neurol Sci; 2022 Sep; 49(5):708-712. PubMed ID: 34663487
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Glial pathology in a novel spontaneous mutant mouse of the Eif2b5 gene: a vanishing white matter disease model.
    Terumitsu-Tsujita M; Kitaura H; Miura I; Kiyama Y; Goto F; Muraki Y; Ominato S; Hara N; Simankova A; Bizen N; Kashiwagi K; Ito T; Toyoshima Y; Kakita A; Manabe T; Wakana S; Takebayashi H; Igarashi H
    J Neurochem; 2020 Jul; 154(1):25-40. PubMed ID: 31587290
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Eukaryotic translation initiation factor 2B and leukoencephalopathy with vanishing white matter].
    Pan YX; Wu Y; Niu ZP; Jiang YW
    Beijing Da Xue Xue Bao Yi Xue Ban; 2009 Oct; 41(5):608-10. PubMed ID: 19829687
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Endoplasmic reticulum stress intolerance in EIF2B3 mutant oligodendrocytes is modulated by depressed autophagy.
    Chen N; Dai L; Jiang Y; Wang J; Hao H; Ren Y; Leng X; Zang L; Wu Y
    Brain Dev; 2016 May; 38(5):507-15. PubMed ID: 26625702
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Postmortem Whole Exome Sequencing Identifies Novel EIF2B3 Mutation With Prenatal Phenotype in 2 Siblings.
    Song H; Haeri S; Vogel H; van der Knaap M; Van Haren K
    J Child Neurol; 2017 Sep; 32(10):867-870. PubMed ID: 28597716
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.