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 *

273 related articles for article (PubMed ID: 4265197)

  • 21. Beta-glucuronidase deficiency in a girl with unusual clinical features.
    Pfeiffer RA; Kresse H; Bäumer N; Sattinger E
    Eur J Pediatr; 1977 Oct; 126(3):155-61. PubMed ID: 144057
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Combination of metachromatic leucodystrophy and mucopolysaccharidosis: a disease entity (mucosulfatidosis)].
    Rampini S; Isler W; Baerlocher K; Bischoff A; Ulrich J; Plüss HJ
    Helv Paediatr Acta; 1970 Nov; 25(5):436-61. PubMed ID: 4250178
    [No Abstract]   [Full Text] [Related]  

  • 23. Sanfilippo syndrome (mucopolysaccharidosis-3).
    Taori GM; Iyer GV; Mokashi S; Balasubramanian KA; Cherian R; Chandi S; Job CK; Bachhawat BK
    J Neurol Sci; 1972 Nov; 17(3):323-45. PubMed ID: 4265908
    [No Abstract]   [Full Text] [Related]  

  • 24. The Sanfilippo syndrome: clinical, biochemical, radiological, haematological and pathological features of nine cases.
    Danks DM; Campbell PE; Cartwright E; Mayne V; Taft LI; Wilson RG
    Aust Paediatr J; 1972 Aug; 8(4):174-86. PubMed ID: 4264725
    [No Abstract]   [Full Text] [Related]  

  • 25. [Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses].
    Passarge E; Wendel U; Wöhler W; Rüdiger HW
    Dtsch Med Wochenschr; 1974 Jan; 99(4):144 passim. PubMed ID: 4274189
    [No Abstract]   [Full Text] [Related]  

  • 26. [Mucopolysaccharidosis VII: report of a case and review of the literature].
    Huang YL; Li SY; Zhao XY; Liu HS; Ou XB; Liu L
    Zhonghua Er Ke Za Zhi; 2011 Jun; 49(6):455-8. PubMed ID: 21924061
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Infantile sialic acid storage disease in two siblings.
    Cooper A; Sardharwalla IB; Thornley M; Ward KP
    J Inherit Metab Dis; 1988; 11 Suppl 2():259-62. PubMed ID: 3141716
    [No Abstract]   [Full Text] [Related]  

  • 28. Correction of murine mucopolysaccharidosis VII by a human beta-glucuronidase transgene.
    Kyle JW; Birkenmeier EH; Gwynn B; Vogler C; Hoppe PC; Hoffmann JW; Sly WS
    Proc Natl Acad Sci U S A; 1990 May; 87(10):3914-8. PubMed ID: 2111021
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Biochemical differentiation of mucopolysaccharidoses].
    Spranger J; Wiedemann HR
    Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):421-3. PubMed ID: 4257110
    [No Abstract]   [Full Text] [Related]  

  • 30. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts.
    Hickman S; Shapiro LJ; Neufeld EF
    Biochem Biophys Res Commun; 1974 Mar; 57(1):55-61. PubMed ID: 4364008
    [No Abstract]   [Full Text] [Related]  

  • 31. [Mucopolysaccharidoses. VI. Genetics of mucopolysaccharidosis. Transmission and frequency].
    Romano C; Vianello MG
    Minerva Pediatr; 1972 Oct; 24(34):1634-41. PubMed ID: 4264145
    [No Abstract]   [Full Text] [Related]  

  • 32. [A new type of mucopolysaccharidosis with athetosis and urinary excretion of keratan sulfate].
    Maroteaux P
    Nouv Presse Med; 1973 Apr; 2(15):975-9. PubMed ID: 4267565
    [No Abstract]   [Full Text] [Related]  

  • 33. Galactokinase deficiency: clinical and biochemical findings in a new kindred.
    Pickering WR; Howell RR
    J Pediatr; 1972 Jul; 81(1):50-5. PubMed ID: 5034870
    [No Abstract]   [Full Text] [Related]  

  • 34. [Electrophoretic and enzymatic analysis of urinary glycosaminoglycans. Application to the study of mucopolysaccharidosis].
    Picard J; Gardais A; Esquivie C
    Pathol Biol (Paris); 1971 Mar; 19(5):285-91. PubMed ID: 4102384
    [No Abstract]   [Full Text] [Related]  

  • 35. Restoration of normal lysosomal function in mucopolysaccharidosis type VII cells by retroviral vector-mediated gene transfer.
    Wolfe JH; Schuchman EH; Stramm LE; Concaugh EA; Haskins ME; Aguirre GD; Patterson DF; Desnick RJ; Gilboa E
    Proc Natl Acad Sci U S A; 1990 Apr; 87(8):2877-81. PubMed ID: 2158095
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hydrocephalus and papilledema in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI).
    Goldberg MF; Scott CI; McKusick VA
    Am J Ophthalmol; 1970 Jun; 69(6):969-75. PubMed ID: 4246483
    [No Abstract]   [Full Text] [Related]  

  • 37. Mucopolysaccharidosis 3 A (Sanfilippo A disease): deficiency of a heparin sulfamidase in skin fibroblasts and leucocytes.
    Kresse H
    Biochem Biophys Res Commun; 1973 Oct; 54(3):1111-8. PubMed ID: 4201808
    [No Abstract]   [Full Text] [Related]  

  • 38. [Mucopolysaccharidosis type VII. Clinical, radiological and biochemical studies in a neonatal case (author's transl)].
    Teyssier G; Maire I; Damon G; Boyer S; Lauras B; Freycon F
    Arch Fr Pediatr; 1981 Oct; 38(8):603-4. PubMed ID: 6797379
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cellular metachromasia, a genetic marker for studying the mucopolysaccharidoses.
    Danes BS; Bearn AG
    Lancet; 1967 Feb; 1(7484):241-3. PubMed ID: 4163146
    [No Abstract]   [Full Text] [Related]  

  • 40. [Effect of mucopolysaccharides on the solubility of lysosomal enzymes].
    Kint JA
    Arch Int Physiol Biochim; 1973 Dec; 81(5):973. PubMed ID: 4133551
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.