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Journal Abstract Search

129 related items for PubMed ID: 1994998

  • 1. [A case of type I hyperprolinemia associated with photogenic epilepsy].
    Ishikawa Y, Kameda K, Okabe M, Imai T, Nagaoka M, Minami R.
    No To Hattatsu; 1991 Jan; 23(1):81-6. PubMed ID: 1994998
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  • 2. Clinical, biochemical and enzymatic studies in type I hyperprolinemia associated with chromosomal abnormality.
    Oyanagi K, Tsuchiyama A, Itakura Y, Tamura Y, Nakao T, Fujita S, Shiono H.
    Tohoku J Exp Med; 1987 Apr; 151(4):465-75. PubMed ID: 3617056
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  • 3. [Hyperprolinemia type I].
    Endo F.
    Ryoikibetsu Shokogun Shirizu; 1998 Apr; (18 Pt 1):152-4. PubMed ID: 9590013
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  • 5. Evidence for association of hyperprolinemia with schizophrenia and a measure of clinical outcome.
    Clelland CL, Read LL, Baraldi AN, Bart CP, Pappas CA, Panek LJ, Nadrich RH, Clelland JD.
    Schizophr Res; 2011 Sep; 131(1-3):139-45. PubMed ID: 21645996
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  • 7. Long-term neuropsychiatric follow-up in hyperprolinemia type I.
    Di Rosa G, Nicotera AG, Lenzo P, Spanò M, Tortorella G.
    Psychiatr Genet; 2014 Aug; 24(4):172-5. PubMed ID: 24842239
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  • 12. Hyperprolinemia induces DNA, protein and lipid damage in blood of rats: antioxidant protection.
    Ferreira AG, Scherer EB, da Cunha AA, Manfredini V, Biancini GB, Vanzin CS, Vargas CR, Wyse AT.
    Int J Biochem Cell Biol; 2014 Sep; 54():20-5. PubMed ID: 24980685
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  • 13. Type II hyperprolinemia: a case report.
    Onenli-Mungan N, Yüksel B, Elkay M, Topaloğlu AK, Baykal T, Ozer G.
    Turk J Pediatr; 2004 Sep; 46(2):167-9. PubMed ID: 15214748
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  • 14. [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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  • 16. FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT.
    EFRON ML.
    N Engl J Med; 1965 Jun 17; 272():1243-54. PubMed ID: 14290545
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