BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 4201594)

  • 1. Mucolipidosis 3 (pseudo-Hurler polydystrophy): cytological and ultrastructural observations of cultured fibroblast cells.
    Taylor HA; Thomas GH; Miller CS; Kelly TE; Siggers D
    Clin Genet; 1973; 4(5):388-97. PubMed ID: 4201594
    [No Abstract]   [Full Text] [Related]  

  • 2. Conjunctival ultrastructure in mucolipidosis 3 (pseudo-Hurler polydystrophy).
    Quigley HA; Goldberg MF
    Invest Ophthalmol; 1971 Aug; 10(8):568-80. PubMed ID: 4255138
    [No Abstract]   [Full Text] [Related]  

  • 3. Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture.
    Tondeur M; Vamos-Hurwitz E; Mockel-Pohl S; Dereume JP; Cremer N; Loeb H
    J Pediatr; 1971 Sep; 79(3):366-78. PubMed ID: 4327937
    [No Abstract]   [Full Text] [Related]  

  • 4. Mucolipidosis 3 (Pseudo-Hurler polydystrophy): multiple lysosomal enzyme abnormalities in serum and cultured fibroblast cells.
    Thomas GH; Taylor HA; Reynolds LW; Miller CS
    Pediatr Res; 1973 Sep; 7(9):751-6. PubMed ID: 4200718
    [No Abstract]   [Full Text] [Related]  

  • 5. An ultrastructural comparison of normal and Hurler syndrome dermal fibroblasts.
    Conrad GW; Sherman D; Dorfman A
    Pediatr Res; 1972 Jun; 6(6):563-75. PubMed ID: 4625815
    [No Abstract]   [Full Text] [Related]  

  • 6. Pseudo-Hurler polydystrophy (mucolipidosis 3). A clinical, biochemical and ultrastructural study.
    Stein H; Berman ER; Livni N; Merin S; Sheskin J; Cohen T
    Isr J Med Sci; 1974 May; 10(5):463-75. PubMed ID: 4213328
    [No Abstract]   [Full Text] [Related]  

  • 7. Mucolipidosis III (pseudo-Hurler polydystrophy).
    Kelly TE; Reynolds CW; Siggers DC
    Birth Defects Orig Artic Ser; 1974; 10(12):478-83. PubMed ID: 4282263
    [No Abstract]   [Full Text] [Related]  

  • 8. Mucolipidosis II (I-cell disease): ultrastructural observations of conjunctiva and skin.
    Kenyon KR; Sensenbrenner JA
    Invest Ophthalmol; 1971 Aug; 10(8):555-67. PubMed ID: 4255137
    [No Abstract]   [Full Text] [Related]  

  • 9. Ultrastructural studies of the skin in Hurler's syndrome.
    DeCloux RJ; Friederici HH
    Arch Pathol; 1969 Oct; 88(4):350-8. PubMed ID: 4241779
    [No Abstract]   [Full Text] [Related]  

  • 10. Roentgen findings in mucolipidosis III (Pseudo-Hurler polydystrophy).
    Melhem R; Dorst JP; Scott CI; McKusick VA
    Radiology; 1973 Jan; 106(1):153-60. PubMed ID: 4264747
    [No Abstract]   [Full Text] [Related]  

  • 11. [Clinical picture, histological and electron microscopy ophthalmic findings in an infant with Pfaundler-Hurler mucopolysaccharidosis].
    Reim H; Rohen JW; Dittrich JK
    Klin Monbl Augenheilkd; 1971 Oct; 159(4):444-56. PubMed ID: 4257466
    [No Abstract]   [Full Text] [Related]  

  • 12. Ultrastructure of cartilage in the Hurler and Sanfilippo syndromes.
    Silberberg R; Rimoin DL; Rosenthal RE; Hasler MB
    Arch Pathol; 1972 Dec; 94(6):500-10. PubMed ID: 4263881
    [No Abstract]   [Full Text] [Related]  

  • 13. Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromes.
    Mueller OT; Shows TB; Opitz JM
    Am J Med Genet; 1984 Jul; 18(3):547-56. PubMed ID: 6433708
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dermatological aspects of pseudo-Hurler polydystrophy (mucolipidosis 3).
    Sheskin J; Stein H
    Int J Dermatol; 1973; 12(6):348-53. PubMed ID: 4202776
    [No Abstract]   [Full Text] [Related]  

  • 15. Fibroblasts from patients with I-cell disease and pseudo-Hurler polydystrophy are deficient in uridine 5'-diphosphate-N-acetylglucosamine: glycoprotein N-acetylglucosaminylphosphotransferase activity.
    Reitman ML; Varki A; Kornfeld S
    J Clin Invest; 1981 May; 67(5):1574-9. PubMed ID: 6262380
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mucopolysaccharidosis type II (Hurler-Hunter) in siblings. Electron microscopic study].
    Tichý J; Cihula J; Vortel V
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1972; 15(2):173-9. PubMed ID: 4209410
    [No Abstract]   [Full Text] [Related]  

  • 17. Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie case.
    Tondeur M; Vamos-Hurwitz E; Cantz M; Cremer N; Libert J; Pardou A
    Acta Paediatr Belg; 1976; 29(2):109-15. PubMed ID: 826105
    [No Abstract]   [Full Text] [Related]  

  • 18. Treatment related observations in solid tissues, fibroblast cultured and amniotic fluid cells of type II glycogenosis, Hurler disease and metachromatic leukodystrophy.
    Hug G; Schubert WK; Soukup S
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):160-83. PubMed ID: 4215475
    [No Abstract]   [Full Text] [Related]  

  • 19. Mucolipidosis III (pseudo-Hurler polydystrophy): Clinical and laboratory studies in a series of 12 patients.
    Kelly TE; Thomas GH; Taylor HA; McKusick VA; Sly WS; Glaser JH; Robinow M; Luzzatti L; Espiritu C; Feingold M; Bull MJ; Ashenhurst EM; Ives EJ
    Johns Hopkins Med J; 1975 Oct; 137(4):156-75. PubMed ID: 810612
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hepatic ultrastructure in the Hurler syndrome.
    Callahan WP; Lorincz AE
    Am J Pathol; 1966 Feb; 48(2):277-98. PubMed ID: 4221940
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.