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 *

146 related articles for article (PubMed ID: 2900478)

  • 1. [Metachromatic leukodystrophy. Results of laboratory chemical, neurophysiologic, histologic and imaging procedures within the scope of a family study].
    Schröder J; Haan J; Haupts M
    Nervenarzt; 1988 May; 59(5):296-8. PubMed ID: 2900478
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bone marrow transplantation in metachromatic leukodystrophy.
    Lipton M; Lockman LA; Ramsay NK; Kersey JH; Jacobson RI; Krivit W
    Birth Defects Orig Artic Ser; 1986; 22(1):57-67. PubMed ID: 2870748
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: a new mutation in the ARSA gene.
    Marcão AM; Wiest R; Schindler K; Wiesmann U; Weis J; Schroth G; Miranda MC; Sturzenegger M; Gieselmann V
    Arch Neurol; 2005 Feb; 62(2):309-13. PubMed ID: 15710861
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Metachromatic leukodystrophy: an exceptional cause of dementia in the adult].
    Pérez Sempere A; Martínez Menéndez B; Villaverde Amundaraín FJ; Rodríguez Vallejo A; Togores Veguero J; Portera Sánchez A
    Neurologia; 1992 May; 7(5):114-6. PubMed ID: 1389290
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy.
    Bisgaard AM; Kirchhoff M; Nielsen JE; Kibaek M; Lund A; Schwartz M; Christensen E
    Clin Genet; 2009 Feb; 75(2):175-9. PubMed ID: 19054018
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Juvenile metachromatic leukodystrophy: evoked potentials and computed tomography.
    Carlin L; Roach ES; Riela A; Spudis E; McLean WT
    Ann Neurol; 1983 Jan; 13(1):105-6. PubMed ID: 6830154
    [No Abstract]   [Full Text] [Related]  

  • 8. Atypical clinical course in juvenile metachromatic leukodystrophy involving novel arylsulfatase A gene mutations.
    Anlar B; Waye JS; Eng B; Oguz KK
    Dev Med Child Neurol; 2006 May; 48(5):383-7. PubMed ID: 16608548
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Isolated peripheral neuropathy in atypical metachromatic leukodystrophy: a recurrent mutation.
    Coulter-Mackie MB; Applegarth DA; Toone JR; Gagnier L; Anzarut AR; Hendson G
    Can J Neurol Sci; 2002 May; 29(2):159-63. PubMed ID: 12035837
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Metachromatic Leukodystrophy (MLD): MRI findings].
    Fenchel M; Hauser TK; Nägele T; Ernemann U; Horger M
    Rofo; 2011 Oct; 183(10):893-5. PubMed ID: 22232791
    [No Abstract]   [Full Text] [Related]  

  • 11. A novel mutation in the arylsulfatase A gene associated with adult-onset metachromatic leukodystrophy without clinical evidence of neuropathy.
    Suzuki C; Watanabe M; Tomiyama M; Sugimoto K; Nanba E; Jackson M; Kimura T; Seino Y; Wakasaya Y; Kawarabayashi T; Miki Y; Yamamoto-Watanabe Y; Shoji M
    Eur Neurol; 2008; 60(6):310-1. PubMed ID: 18832844
    [No Abstract]   [Full Text] [Related]  

  • 12. [Arylsulfatase A deficiency-metachromatic leukodystrophy].
    Eto Y
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):749-52. PubMed ID: 2908400
    [No Abstract]   [Full Text] [Related]  

  • 13. Late-onset metachromatic leukodystrophy: genotype strongly influences phenotype.
    Rauschka H; Colsch B; Baumann N; Wevers R; Schmidbauer M; Krammer M; Turpin JC; Lefevre M; Olivier C; Tardieu S; Krivit W; Moser H; Moser A; Gieselmann V; Zalc B; Cox T; Reuner U; Tylki-Szymanska A; Aboul-Enein F; LeGuern E; Bernheimer H; Berger J
    Neurology; 2006 Sep; 67(5):859-63. PubMed ID: 16966551
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Homozygote for mutation c.1204 + 1G > A of the ARSA gene presents with a late-infantile form of metachromatic leukodystrophy and a rare MRI white matter lesion type.
    Ługowska A; Szymańska K; Kmiec T; Tarczyńska I; Czartoryska B; Tylki-Szymańska A; Jurkiewicz E
    J Appl Genet; 2005; 46(3):337-9. PubMed ID: 16110195
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Metachromatic leukodystrophy. Late juvenile form. Review of 6 cases].
    Campistol Plana J; Colomer Orefil J; Poo Argüelles P; Vernet Bori A; Fernández Alvarez E
    An Esp Pediatr; 1983 Jul; 19(1):41-8. PubMed ID: 6139050
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MRI appearances of metachromatic leukodystrophy.
    Faerber EN; Melvin J; Smergel EM
    Pediatr Radiol; 1999 Sep; 29(9):669-72. PubMed ID: 10460327
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A 5-year-old male child with late infantile metachromatic leukodystrophy: a case report.
    Mahmood A; Chacham S; Reddy UN; Rao JN; Rao SP
    J Child Neurol; 2015 Mar; 30(4):483-5. PubMed ID: 25117420
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Juvenile form of metachromatic leukodystrophy. Clinical variant of sulfatidosis].
    Turpin JC; Elchardus JF; Morice J; Georges MC; Dubois G
    Pediatrie; 1978; 3(7):629-36. PubMed ID: 33363
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.