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Journal Abstract Search

100 related items for PubMed ID: 4420280

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  • 3. [Familial hyperprolinemia with nephropathy].
    Ortuño Mirete J, Guardiola Vicente JM, Botella García J.
    Rev Clin Esp; 1970 Jul 31; 118(2):141-50. PubMed ID: 5486371
    [No Abstract] [Full Text] [Related]

  • 4. [Familial essential hyperprolinemia].
    Hainaut H, Hariga J, Willems C, Heusden A, Chapelle P.
    Presse Med (1893); 1971 Apr 24; 79(21):945-8. PubMed ID: 5580522
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  • 5. Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family.
    Mollica F, Pavone L, Antener I.
    Pediatrics; 1971 Aug 24; 48(2):225-31. PubMed ID: 5560617
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  • 9. [Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy].
    Jeune M, Collombel C, Michel M, David M, Guibaud P, Guerrier G, Albert J.
    Ann Pediatr (Paris); 1970 Feb 02; 17(2):349-63. PubMed ID: 5513158
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  • 10. [Renal clearance of amino acid in a hyperprolinemic child].
    Dodinval P, Willems C, Heusden AM, Hainaut H, Gottschalk C.
    J Genet Hum; 1969 Oct 02; 17(3):297-315. PubMed ID: 5387412
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  • 11. [Hyperprolinemia and hydroxyprolinemia].
    Berger R, Broyer M.
    Presse Med (1893); 1969 May 28; 77(26):957-8. PubMed ID: 5795142
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  • 13. [Diseases caused by altered intermediate metabolism of amino acids].
    Bulgarelli R, Berio A.
    Minerva Nipiol; 1969 May 28; 19(6):328-61 contd. PubMed ID: 4923874
    [No Abstract] [Full Text] [Related]

  • 14. Intravenous proline tolerance in a patient with hyperprolinaemia type II and his relatives.
    Similä S.
    Helv Paediatr Acta; 1970 Jul 28; 25(3):287-92. PubMed ID: 5518053
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  • 17. Familial hyperprolinemia and mental retardation. A second metabolic type.
    Selkoe DJ.
    Neurology; 1969 May 28; 19(5):494-502. PubMed ID: 5815222
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  • 18. Hyperprolinaemia type II.
    Similä S.
    Fla Dent J; 1970 Aug 28; 2(2):143-50. PubMed ID: 5271041
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  • 19. [Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)].
    Minder FC, Dubach UC, Antener I.
    Z Klin Med; 1965 Dec 31; 158(7):601-32. PubMed ID: 5869106
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  • 20. [Results of a survey of search of amino-acidopathies in the north of France. Apropos of 8,433 children].
    Fontaine G, Farriaux JP, Delecour M.
    Ann Pediatr (Paris); 1970 Dec 31; 17(6):487-9. PubMed ID: 5421331
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