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.
4. 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]
5. [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]
6. [Differentiation between arylsulfatase A deficiency and pseudo-deficiency]. Horovenko NH; Ol'khovych NV Ukr Biokhim Zh (1999); 2003; 75(5):106-11. PubMed ID: 14682002 [TBL] [Abstract][Full Text] [Related]
7. Co-occurrence of Metachromatic Leukodystrophy in Phelan-McDermid Syndrome. Mingbunjerdsuk D; Wong M; Bozarth X; Sun A J Child Neurol; 2021 Feb; 36(2):148-151. PubMed ID: 32991243 [TBL] [Abstract][Full Text] [Related]
8. Sulfatide excreting heterozygous carrier of juvenile metachromatic leukodystrophy or asymptomatic patient of adult metachromatic leukodystrophy. Harzer K; Recke AS Humangenetik; 1975 Oct; 29(4):299-307. PubMed ID: 1176145 [TBL] [Abstract][Full Text] [Related]
9. Arylsulfatases A and B in metachromatic leukodystrophy and Maroteaux-Lamy syndrome: studies with 4-methylumelliferyl sulfate. Kolodny EH; Mumford RA Adv Exp Med Biol; 1976; 68():239-51. PubMed ID: 7105 [TBL] [Abstract][Full Text] [Related]
10. Characterization of urinary sulfatides in metachromatic leukodystrophy using electrospray ionization-tandem mass spectrometry. Whitfield PD; Sharp PC; Johnson DW; Nelson P; Meikle PJ Mol Genet Metab; 2001 May; 73(1):30-7. PubMed ID: 11350180 [TBL] [Abstract][Full Text] [Related]
11. Adult-type metachromatic leukodystrophy with a compound heterozygote mutation showing character change and dementia. Fukutani Y; Noriki Y; Sasaki K; Isaki K; Kuriyama M; Kurosawa K; Ida H Psychiatry Clin Neurosci; 1999 Jun; 53(3):425-8. PubMed ID: 10459747 [TBL] [Abstract][Full Text] [Related]
12. An unusual homozygous arylsulfatase: a pseudodeficiency in a metachromatic leukodystrophy Tunisian patient. Tinsa F; Caillaud C; Vanier MT; Bousnina D; Boussetta K; Bousnina S J Child Neurol; 2010 Jan; 25(1):82-6. PubMed ID: 19574581 [TBL] [Abstract][Full Text] [Related]
13. Quantification of plasma sulfatides by mass spectrometry: Utility for metachromatic leukodystrophy. Saville JT; Smith NJ; Fletcher JM; Fuller M Anal Chim Acta; 2017 Feb; 955():79-85. PubMed ID: 28088283 [TBL] [Abstract][Full Text] [Related]
14. A variant form of metachromatic leukodystrophy without arylsulfatase deficiency. Hahn AF; Gordon BA; Hinton GG; Gilbert JJ Ann Neurol; 1982 Jul; 12(1):33-6. PubMed ID: 6126151 [TBL] [Abstract][Full Text] [Related]
15. Seizures as a presenting feature of late onset metachromatic leukodystrophy. Bostantjopoulou S; Katsarou Z; Michelakaki H; Kazis A Acta Neurol Scand; 2000 Sep; 102(3):192-5. PubMed ID: 10987380 [TBL] [Abstract][Full Text] [Related]