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Journal Abstract Search

131 related items for PubMed ID: 4663888

  • 41. Electroencephalographic findings in three patients with nonketotic hyperglycinemia.
    Seppäläinen AM, Similä S.
    Epilepsia; 1971 Mar; 12(1):101-7. PubMed ID: 5282878
    [No Abstract] [Full Text] [Related]

  • 42. Pyroglutamic aciduria in propionyl CoA carboxylase deficiency.
    Morishita H, Nagaya S, Nakajima T, Kawase A, Ohya A, Sugiyama S, Kamiya K, Watanabe I, Togari H, Suzuki Y.
    J Inherit Metab Dis; 1984 Mar; 7(3):139-40. PubMed ID: 6438400
    [No Abstract] [Full Text] [Related]

  • 43. Genetic diagnostic studies for mental retardation.
    Beaudet AL.
    Curr Probl Pediatr; 1978 Mar; 8(5):1-47. PubMed ID: 657833
    [No Abstract] [Full Text] [Related]

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  • 46. [Hereditary amino acid metabolism disorders. Indications for early diagnosis].
    Kroll S, Zebisch P, Toussaint W.
    Fortschr Med; 1972 Apr 13; 90(11):423-8. PubMed ID: 4680607
    [No Abstract] [Full Text] [Related]

  • 47. [Screening test detection of genetic errors of metabolism in children with hearing defects (author's transl)].
    Lubs H, Baumann H, Kluge G, Machill G.
    Laryngol Rhinol Otol (Stuttg); 1974 Sep 13; 53(9):648-51. PubMed ID: 4419508
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  • 49. [Prolinuria].
    Tada K.
    Saishin Igaku; 1969 Jun 13; 24(6):1226-34. PubMed ID: 5805578
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  • 52. Further investigations in hyperargininemia.
    Van Sande M, Terheggen HG, Colombo JP, Lowenthal A, Rogers S, Schwenk A.
    Monogr Hum Genet; 1972 Jun 13; 6():143. PubMed ID: 4663887
    [No Abstract] [Full Text] [Related]

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  • 56. A rare cause of high anion gap metabolic acidosis.
    Milosevic S, Tran K, O'Brien B.
    Intern Med J; 2013 Jan 13; 43(1):100-1. PubMed ID: 23324093
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  • 59. [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
    [No Abstract] [Full Text] [Related]

  • 60. Iminoaciduria.
    Blattner RJ.
    J Pediatr; 1969 Jan 02; 74(1):144-6. PubMed ID: 5782820
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