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 *

120 related articles for article (PubMed ID: 27606023)

  • 1. Diffusion-weighted magnetic resonance imaging findings in a case of metachromatic leukodystrophy.
    Singh P; Kaur R
    J Pediatr Neurosci; 2016; 11(2):131-3. PubMed ID: 27606023
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Diffusion-weighted imaging findings in juvenile metachromatic leukodystrophy.
    Oguz KK; Anlar B; Senbil N; Cila A
    Neuropediatrics; 2004 Oct; 35(5):279-82. PubMed ID: 15534760
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Metachromatic leukodystrophy. Diffusion MR imaging and proton MR spectroscopy.
    Sener RN
    Acta Radiol; 2003 Jul; 44(4):440-3. PubMed ID: 12846696
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A closer look at ARSA activity in a patient with metachromatic leukodystrophy.
    Doherty K; Frazier SB; Clark M; Childers A; Pruthi S; Wenger DA; Duis J
    Mol Genet Metab Rep; 2019 Jun; 19():100460. PubMed ID: 30828547
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adult metachromatic leukodystrophy. Value of computed tomographic scanning and magnetic resonance imaging of the brain.
    Waltz G; Harik SI; Kaufman B
    Arch Neurol; 1987 Feb; 44(2):225-7. PubMed ID: 3813937
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Metachromatic leukodystrophy: diffusion MR imaging findings.
    Sener RN
    AJNR Am J Neuroradiol; 2002 Sep; 23(8):1424-6. PubMed ID: 12223391
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Metachromatic leukodystrophy: magnetic resonance imaging (diffusion weighted image--DWI).
    Seidl Z; Vaneckova M; Vitak T
    Neuro Endocrinol Lett; 2008 Aug; 29(4):428-30. PubMed ID: 18766149
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Electroneurography and Advanced Neuroimaging Profile in Pediatric-onset Metachromatic Leukodystrophy.
    Raina A; Nair SS; Nagesh C; Thomas B; Nair M; Sundaram S
    J Pediatr Neurosci; 2019; 14(2):70-75. PubMed ID: 31516623
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Rare Case of Metachromatic Leukodystrophy Confirmed by Arylsulfatase A.
    Alam ST; Akhter S; Rahman MM; Islam KA; Siddique R; Helaly L; Ahmed S
    Mymensingh Med J; 2015 Oct; 24(4):864-7. PubMed ID: 26620033
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Metachromatic Leukodystrophy. Case Presentation].
    Espejo LM; de la Espriella R; Hernández JF
    Rev Colomb Psiquiatr; 2017; 46(1):44-49. PubMed ID: 28193373
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intestinal involvement in metachromatic leukodystrophy.
    Yavuz H; Yüksekkaya HA
    J Child Neurol; 2011 Jan; 26(1):117-20. PubMed ID: 21212458
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Late infantile metachromatic leukodystrophy: case report].
    Alvarez-Pabón Y; Lozano-Jiménez JF; Di Lizio-Miele KG; Contreras-García GA
    Arch Argent Pediatr; 2019 Feb; 117(1):e52-e55. PubMed ID: 30652456
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Saposin B-Deficient Metachromatic Leukodystrophy Mimicking Acute Flaccid Paralysis.
    Madaan P; Jauhari P; Chakrabarty B; Kumar A; Gulati S
    Neuropediatrics; 2019 Oct; 50(5):318-321. PubMed ID: 31319425
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Infantile metachromatic leukodystrophy in an 18 month old girl.
    Ali Mallick MS; Godil A; Khetpal A; Rizvi AH; Khan F
    J Pak Med Assoc; 2016 Sep; 66(9):1197-1200. PubMed ID: 27654749
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A homozygote for the c.459+1G>A mutation in the ARSA gene presents with cerebellar ataxia as the only first clinical sign of metachromatic leukodystrophy.
    Lugowska A; Mierzewska H; Bekiesińska-Figatowska M; Szczepanik E; Goszczańska-Ciuchta A; Bednarska-Makaruk M
    J Neurol Sci; 2014 Mar; 338(1-2):214-7. PubMed ID: 24411407
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sixteen novel mutations in the arylsulfatase A gene causing metachromatic leukodystrophy.
    Luzi P; Rafi MA; Rao HZ; Wenger DA
    Gene; 2013 Nov; 530(2):323-8. PubMed ID: 24001781
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The clinical features and diagnosis of Metachromatic leukodystrophy: A case series of Iranian Pediatric Patients.
    Jabbehdari S; Rahimian E; Jafari N; Sanii S; Khayatzadehkakhki S; Nejad Biglari H
    Iran J Child Neurol; 2015; 9(3):57-61. PubMed ID: 26401154
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: a case report and phenotypic comparison with a previously reported case.
    Hayashi T; Nakamura M; Ichiba M; Matsuda M; Kato M; Shiokawa N; Shimo H; Tomiyasu A; Mori S; Tomiyasu Y; Ishizuka T; Inamori Y; Okamoto Y; Umehara F; Arimura K; Nakabeppu Y; Sano A
    Psychiatry Clin Neurosci; 2011 Feb; 65(1):105-8. PubMed ID: 21265945
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Apolipoprotein E genotype and LRP1 polymorphisms in patients with different clinical types of metachromatic leukodystrophy.
    Ługowska A; Musielak M; Jamroz E; Pyrkosz A; Kmieć T; Tylki-Szymańska A; Bednarska-Makaruk M
    Gene; 2013 Sep; 526(2):176-81. PubMed ID: 23701968
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pathology of the gallbladder in a child with metachromatic leukodystrophy.
    McFadden K; Ranganathan S
    Pediatr Dev Pathol; 2015; 18(3):228-30. PubMed ID: 25569213
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.