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 *

128 related articles for article (PubMed ID: 35387852)

  • 1. Teaching NeuroImage:
    Cherian A; Yalapalli MK; K P D; Vijayaraghavan A; Sundaram S
    Neurology; 2022 Jun; 98(24):1029-1030. PubMed ID: 35387852
    [No Abstract]   [Full Text] [Related]  

  • 2. Phenotypic spectrum of mutations in IBA57, a candidate gene for cavitating leukoencephalopathy.
    Liu M; Zhang J; Zhang Z; Zhou L; Jiang Y; Wang J; Xiao J; Wu Y
    Clin Genet; 2018 Feb; 93(2):235-241. PubMed ID: 28671726
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genotypic Spectrum and Natural History of Cavitating Leukoencephalopathies in Childhood.
    Zhang J; Liu M; Zhang Z; Zhou L; Kong W; Jiang Y; Wang J; Xiao J; Wu Y
    Pediatr Neurol; 2019 May; 94():38-47. PubMed ID: 30770271
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy.
    Debray FG; Stümpfig C; Vanlander AV; Dideberg V; Josse C; Caberg JH; Boemer F; Bours V; Stevens R; Seneca S; Smet J; Lill R; van Coster R
    J Inherit Metab Dis; 2015 Nov; 38(6):1147-53. PubMed ID: 25971455
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome.
    Zhan F; Liu X; Ni R; Liu T; Cao Y; Wu J; Tian W; Luan X; Cao L
    Metab Brain Dis; 2022 Feb; 37(2):311-317. PubMed ID: 34709542
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Teaching NeuroImages: MRI findings in an infant with cavitating leukoencephalopathy.
    Hong A; Assaad P; Karkare S
    Neurology; 2019 Feb; 92(8):e884-e885. PubMed ID: 30777920
    [No Abstract]   [Full Text] [Related]  

  • 7. Teaching Neuro
    Villar-Quiles RN; Gómez-Ruiz N; Jorquera-Moya M; Matías-Guiu J; Matias-Guiu JA
    Neurology; 2017 Mar; 88(12):e113-e114. PubMed ID: 28320930
    [No Abstract]   [Full Text] [Related]  

  • 8. Axenfeld-Rieger Syndrome and Leukoencephalopathy Caused by a Mutation in FOXC1.
    Kumar M; Chambers C; Dhamija R
    Pediatr Neurol; 2017 Jan; 66():113-114. PubMed ID: 27697311
    [No Abstract]   [Full Text] [Related]  

  • 9. Cavitating leukodystrophy in a case of mitochondrial complex III deficiency due to LYRM7 mutation.
    Rezaei M; Dourandish Z; Kiani Mehr G; Ghorbani A; Fatehi F
    Acta Neurol Belg; 2024 Aug; 124(4):1409-1410. PubMed ID: 38592654
    [No Abstract]   [Full Text] [Related]  

  • 10. Homozygous mutation in the APOA1BP is associated with a lethal infantile leukoencephalopathy.
    Spiegel R; Shaag A; Shalev S; Elpeleg O
    Neurogenetics; 2016 Jul; 17(3):187-90. PubMed ID: 27122014
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An unusual cause of cavitating leukoencephalopathy: ethylmalonic encephalopathy.
    Cavusoglu D; Hismi BO; Dundar NO; Oztekin O; Koc A; Canda E; Arican P; Gencpinar P
    Acta Neurol Belg; 2018 Jun; 118(2):309-312. PubMed ID: 29464661
    [No Abstract]   [Full Text] [Related]  

  • 12. Cavitating leukoencephalopathy in a child carrying the mitochondrial A8344G mutation.
    Biancheri R; Rossi D; Cassandrini D; Rossi A; Bruno C; Santorelli FM
    AJNR Am J Neuroradiol; 2010 Oct; 31(9):E78-9. PubMed ID: 20581069
    [No Abstract]   [Full Text] [Related]  

  • 13. Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes.
    Torraco A; Ardissone A; Invernizzi F; Rizza T; Fiermonte G; Niceta M; Zanetti N; Martinelli D; Vozza A; Verrigni D; Di Nottia M; Lamantea E; Diodato D; Tartaglia M; Dionisi-Vici C; Moroni I; Farina L; Bertini E; Ghezzi D; Carrozzo R
    J Neurol; 2017 Jan; 264(1):102-111. PubMed ID: 27785568
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 'De novo' Col4A2 mutation in a patient with migraine, leukoencephalopathy, and small carotid aneurysms.
    Kollmann P; Peeters A; Vanakker O; Sznajer Y
    J Neurol; 2016 Nov; 263(11):2327-2329. PubMed ID: 27624120
    [No Abstract]   [Full Text] [Related]  

  • 15. Mystery Case: CSF-1R mutation is a cause of intracranial cerebral calcifications, cysts, and leukoencephalopathy.
    Ayrignac X; Mouzat K; Magnin E; Berger E; Carra-Dallière C; Lumbroso S; Labauge P
    Neurology; 2016 Nov; 87(22):e262-e263. PubMed ID: 27895249
    [No Abstract]   [Full Text] [Related]  

  • 16. Cavitating Leukoencephalopathy With Posterior Predominance Caused by a Deletion in the APOPT1 Gene in an Indian Boy.
    Sharma S; Singh P; Fernandez-Vizarra E; Zeviani M; Van der Knaap MS; Saran RK
    J Child Neurol; 2018 May; 33(6):428-431. PubMed ID: 29577824
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Teaching NeuroImage: Partially Reversible Widespread Leukoencephalopathy Associated With Atypical Hemolytic Uremic Syndrome.
    Cani I; Righini M; Cenni P; Foschi M
    Neurology; 2022 Dec; 99(24):1128-1129. PubMed ID: 36130844
    [No Abstract]   [Full Text] [Related]  

  • 18. Author Response: Teaching NeuroImage: Partially Reversible Widespread Leukoencephalopathy Associated With Atypical Hemolytic Uremic Syndrome.
    Foschi M; Cani I; Cenni P; Righini M
    Neurology; 2023 Oct; 101(17):770. PubMed ID: 37871975
    [No Abstract]   [Full Text] [Related]  

  • 19. Reader Response: Teaching NeuroImage: Partially Reversible Widespread Leukoencephalopathy Associated With Atypical Hemolytic Uremic Syndrome.
    Graber J
    Neurology; 2023 Oct; 101(17):769. PubMed ID: 37871974
    [No Abstract]   [Full Text] [Related]  

  • 20. Handwriting impairment in a case of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia caused by a novel mutation in the CSF1R gene.
    Tsai MC; Sung YF
    Neurol Sci; 2022 Mar; 43(3):2109-2110. PubMed ID: 35022934
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.