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 *

125 related articles for article (PubMed ID: 9880143)

  • 1. Pathologic findings of multiple sulfatase deficiency reflect the pattern of enzyme deficiencies.
    Macaulay RJ; Lowry NJ; Casey RE
    Pediatr Neurol; 1998 Nov; 19(5):372-6. PubMed ID: 9880143
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Multiple sulfatase deficiency with a novel biochemical presentation.
    Constantopoulos G
    Eur J Pediatr; 1988 Aug; 147(6):634-8. PubMed ID: 2903054
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multiple sulfatase deficiency.
    Soong BW; Casamassima AC; Fink JK; Constantopoulos G; Horwitz AL
    Neurology; 1988 Aug; 38(8):1273-5. PubMed ID: 2899861
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Arylsulfatases A and B in EBV-transformed lymphoid cell lines: studies on their molecular forms in cells from patients with inborn sulfatase deficiencies. Comparative diagnostic value of enzymatic assays.
    Tempesta MC; Levade T; Salvayre R
    Clin Chim Acta; 1991 Oct; 202(3):149-65. PubMed ID: 1687673
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic complementation studies of multiple sulfatase deficiency.
    Horwitz AL
    Proc Natl Acad Sci U S A; 1979 Dec; 76(12):6496-9. PubMed ID: 118467
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multiple deficiency of mucopolysaccharide sulfatases in mucosulfatidosis.
    Basner R; von Figura K; Glössl J; Klein U; Kresse H; Mlekusch W
    Pediatr Res; 1979 Dec; 13(12):1316-8. PubMed ID: 523191
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiple sulfatase deficiency: bridge between neuronal storage diseases and leukodystrophies.
    Kepes JJ; Berry A; Zacharias DL
    Pathology; 1988 Jul; 20(3):285-91. PubMed ID: 2974530
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ocular features of multiple sulfatase deficiency and a new variant of metachromatic leukodystrophy.
    Bateman JB; Philippart M; Isenberg SJ
    J Pediatr Ophthalmol Strabismus; 1984; 21(4):133-9. PubMed ID: 6470909
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivo.
    Eto Y; Numaguchi S; Tahara T; Rennert OM
    Eur J Pediatr; 1980 Oct; 135(1):85-9. PubMed ID: 7449794
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Arylsulfatase deficiency and various metabolic diseases].
    Czyzewska K; Działoszyński L
    Pediatr Pol; 1978 Sep; 53(9):1129-35. PubMed ID: 30935
    [No Abstract]   [Full Text] [Related]  

  • 11. Multiple sulfatase deficiency: clinical, neuropathological, ultrastructural and biochemical studies.
    Guerra WF; Verity MA; Fluharty AL; Nguyen HT; Philippart M
    J Neuropathol Exp Neurol; 1990 Jul; 49(4):406-23. PubMed ID: 1694540
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Saudi variant of multiple sulfatase deficiency.
    al Aqeel A; Ozand PT; Brismar J; Gascon GG; Brismar G; Nester M; Sakati N
    J Child Neurol; 1992 Apr; 7 Suppl():S12-21. PubMed ID: 1588009
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification.
    Schlotawa L; Adang LA; Radhakrishnan K; Ahrens-Nicklas RC
    Int J Mol Sci; 2020 May; 21(10):. PubMed ID: 32414121
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.
    Chang PL; Davidson RG
    Proc Natl Acad Sci U S A; 1980 Oct; 77(10):6166-70. PubMed ID: 6108562
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SUMF1 enhances sulfatase activities in vivo in five sulfatase deficiencies.
    Fraldi A; Biffi A; Lombardi A; Visigalli I; Pepe S; Settembre C; Nusco E; Auricchio A; Naldini L; Ballabio A; Cosma MP
    Biochem J; 2007 Apr; 403(2):305-12. PubMed ID: 17206939
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ichthyosis: the skin manifestation of multiple sulfatase deficiency.
    Castaño Suárez E; Segurado Rodríguez A; Guerra Tapia A; Simón de las Heras R; López-Ríos F; Coll Rosell MJ
    Pediatr Dermatol; 1997; 14(5):369-72. PubMed ID: 9336808
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Case of multiple sulfatase deficiency and ocular albinism: a diagnostic odyssey.
    Prasad C; Rupar CA; Campbell C; Napier M; Ramsay D; Tay KY; Sharan S; Prasad AN
    Can J Neurol Sci; 2014 Sep; 41(5):626-31. PubMed ID: 25373814
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Early manifestations of multiple sulfatase deficiency.
    Burk RD; Valle D; Thomas GH; Miller C; Moser A; Moser H; Rosenbaum KN
    J Pediatr; 1984 Apr; 104(4):574-8. PubMed ID: 6142938
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Various sulfatase activities in leukocytes and cultured skin fibroblasts from heterozygotes for the multiple sulfatase deficiency (mukosulfatidosis).
    Eto Y; Tahara T; Tokoro T; Maekawa K
    Pediatr Res; 1983 Feb; 17(2):97-100. PubMed ID: 6572356
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A systematic review and meta-analysis of published cases reveals the natural disease history in multiple sulfatase deficiency.
    Schlotawa L; Preiskorn J; Ahrens-Nicklas R; Schiller S; Adang LA; Gärtner J; Friede T
    J Inherit Metab Dis; 2020 Nov; 43(6):1288-1297. PubMed ID: 32621519
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.