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 *

80 related articles for article (PubMed ID: 131525)

  • 61. I-cell disease, mucolipidosis II. Pathological, histochemical, ultrastructural and biochemical observations in four cases.
    Gilbert EF; Dawson G; zu Rhein GM; Opitz JM; Spranger
    Z Kinderheilkd; 1973; 114(4):259-92. PubMed ID: 4353613
    [No Abstract]   [Full Text] [Related]  

  • 62. [Case of dysostosis multiplex with features of mucolipidosis II (I-cell disease)].
    Barylak A
    Pol Przegl Radiol Med Nukl; 1974; 38(5):617-22. PubMed ID: 4374690
    [No Abstract]   [Full Text] [Related]  

  • 63. Hepatic ultrastructure and histochemistry in mucolipidosis II (I-cell disease).
    Kenyon KR; Sensenbrenner JA; Wyllie RG
    Pediatr Res; 1973 Jun; 7(6):560-8. PubMed ID: 4122673
    [No Abstract]   [Full Text] [Related]  

  • 64. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome).
    Martin R; Beck M; Eng C; Giugliani R; Harmatz P; Muñoz V; Muenzer J
    Pediatrics; 2008 Feb; 121(2):e377-86. PubMed ID: 18245410
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Inborn errors of organic acid metabolism.
    Green A
    Br J Hosp Med; 1989 May; 41(5):426-30, 432, 434. PubMed ID: 2663104
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Ganglioside storage diseases.
    O'Brien JS
    Adv Hum Genet; 1972; 3():39-98. PubMed ID: 4268938
    [No Abstract]   [Full Text] [Related]  

  • 67. [Proceedings: Type II mucolipidosis. Discussion of the physiopathol problem apropos of a new case].
    Farriaux JP; Dubois O; Blanckaert D; Walbaum R; Richard P; Halle B; Fontaine G; Strecker G; Tondeur M; Leroy J; Martin JJ
    Arch Fr Pediatr; 1975 Mar; 32(3):294-5. PubMed ID: 131525
    [No Abstract]   [Full Text] [Related]  

  • 68. Affinity chromatography of enzymes hydrolyzing sphingolipids.
    Sloan HR
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):62-5. PubMed ID: 4611538
    [No Abstract]   [Full Text] [Related]  

  • 69. [Biochemical aspects of sphingolipidosis].
    Douste-Blazy L; Thouvenot JP
    Ann Biol Clin (Paris); 1972; 30(6):623-35. PubMed ID: 4569435
    [No Abstract]   [Full Text] [Related]  

  • 70. [Hereditary disorders of lipid metabolism. Screening of lipids].
    Adriaenssens K
    Maandschr Kindergeneeskd; 1969 Jun; 37(1):17-27. PubMed ID: 4307104
    [No Abstract]   [Full Text] [Related]  

  • 71.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 72.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 73.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 74.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 75.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 76.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 77.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 78.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 79.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 80.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]     [New Search]
    of 4.