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PUBMED FOR HANDHELDS

Journal Abstract Search


167 related items for PubMed ID: 4242894

  • 41. [Suspected clinical diagnosis of genetic metabolic disorders in prevention and daily practice].
    Grosser V, Knapp A.
    Z Arztl Fortbild (Jena); 1973 Dec 15; 67(24):1233-8. PubMed ID: 4791811
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  • 44. Study of hereditary metabolic diseases using in vitro techniques.
    Hsia DY.
    Metabolism; 1970 Apr 15; 19(4):309-39. PubMed ID: 4190983
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  • 51. [2 cases of congenital mucopolysaccharidosis].
    Pilosov GA, Pilosova LIa.
    Klin Med (Mosk); 1992 Apr 15; 70(7-8):55-7. PubMed ID: 1460830
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  • 52. [Mucopolysaccharidoses. II. Biochemical study of mucopolysaccharidoses].
    Calatroni A.
    Minerva Pediatr; 1972 Oct 06; 24(34):1579-98. PubMed ID: 4264141
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  • 53. Histochemistry in the study of the ocular manifestations of inherited metabolic disorders.
    Garner A.
    Birth Defects Orig Artic Ser; 1976 Oct 06; 12(3):67. PubMed ID: 60148
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  • 55. [Hereditary mucopolysaccharidoses].
    Orii T.
    Iryo; 1972 May 06; 26(5):381-96. PubMed ID: 4261092
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  • 56. Vascular and connective tissue features in 5 Italian patients with homocystinuria.
    Evangelisti L, Lucarini L, Attanasio M, Porciani MC, Romano E, Prisco D, Gensini GF, Abbate R, Pepe G.
    Int J Cardiol; 2009 May 15; 134(2):251-4. PubMed ID: 18280597
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  • 57. Homocystinuria and Marfanoid appearance.
    Neetens A, De Smet N, Verschueren C, Zelencova L.
    Bull Soc Belge Ophtalmol; 1980 May 15; 191():29-37. PubMed ID: 6979368
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  • 58. Ocular manifestations of the Marfan syndrome.
    Allen RA, Straatsma BR, Apt L, Hall MO.
    Trans Am Acad Ophthalmol Otolaryngol; 1967 May 15; 71(1):18-38. PubMed ID: 4963574
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  • 59. [Congenital metabolic disorders with eye manifestations].
    Oura T, Kozaki M.
    Ganka; 1969 Nov 15; 11(11):872-83. PubMed ID: 5391925
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  • 60. Inborn metabolic disorders with associated ocular lesions in Northern Ireland.
    Martin VA, Carson NA.
    Trans Ophthalmol Soc U K (1962); 1967 Nov 15; 87():847-70. PubMed ID: 5255262
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