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Journal Abstract Search

176 related items for PubMed ID: 4264747

  • 1. 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]

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  • 3. The Hurler syndrome without abnormal mucopolysacchariduria.
    Steinbach HL, Preger L, Williams HE, Cohen P.
    Radiology; 1968 Mar; 90(3):472-8. PubMed ID: 4230591
    [No Abstract] [Full Text] [Related]

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  • 5. A bone dysplasia with deafness.
    Insley J, Astley R.
    Br J Radiol; 1974 May; 47(557):244-51. PubMed ID: 4830146
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  • 7. 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]

  • 8. Atypical Hurler syndrome without alpha-L-iduronidase deficiency.
    Orii T, Sukegawa K, Minami R, Matsuura Y, Tsugawa S.
    Tohoku J Exp Med; 1976 Oct; 120(2):113-23. PubMed ID: 136068
    [Abstract] [Full Text] [Related]

  • 9. [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]

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

  • 11. Progessive diaphyseal dysplasia. Review of the literature and report of seven cases in one family.
    Hundley JD, Wilson FC.
    J Bone Joint Surg Am; 1973 Apr; 55(3):461-74. PubMed ID: 4703201
    [No Abstract] [Full Text] [Related]

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  • 13. Roentgenographic manifestations of Leroy's I-cell disease.
    Taber P, Gyepes MT, Philippart M, Ling S.
    Am J Roentgenol Radium Ther Nucl Med; 1973 May; 118(1):213-21. PubMed ID: 4267400
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  • 15. [Chondrodystrophia related to polyepiphyseal dysplasia and associated with osteolytic shadows, in a child with neurologic disorders].
    Grossiord A, Pannier S, Piera JB, Maroteaux P, Beaupère-Duval G, Asparre M, Quinet I.
    Ann Med Interne (Paris); 1971 Apr; 122(4):447-56. PubMed ID: 5559822
    [No Abstract] [Full Text] [Related]

  • 16. An unusual familial spondyloepiphyseal dysplasia: "spondyloperipheral dysplasia".
    Kelly TE, Lichtenstein JR, Dorst JP.
    Birth Defects Orig Artic Ser; 1977 Apr; 13(3B):149-65. PubMed ID: 407956
    [No Abstract] [Full Text] [Related]

  • 17. A "calcified suprasellar mass" in association with spondylometaphyseal dysplasia.
    Strand RD, Green B.
    Ann Radiol (Paris); 1974 Apr; 17(4):369-74. PubMed ID: 4447311
    [No Abstract] [Full Text] [Related]

  • 18. Progeria. Hutchinson-Gilford syndrome.
    Margolin FR, Steinbach HL.
    Am J Roentgenol Radium Ther Nucl Med; 1968 May; 103(1):173-8. PubMed ID: 5648940
    [No Abstract] [Full Text] [Related]

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  • 20. The spectrum of x-ray manifestations in Cockayne's syndrome.
    Bensman A, Frauré C, Kaufmann HJ.
    Skeletal Radiol; 1981 May; 7(3):173-7. PubMed ID: 7330673
    [No Abstract] [Full Text] [Related]

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