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Journal Abstract Search

145 related items for PubMed ID: 18197084

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  • 3. Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
    Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, Drouin-Garraud V, Lemarchand M, Philip N, Gérard-Desplanches A, Carlier M, Philippe A, Nolen MC, Heron D, Sarda P, Lacombe D, Coizet C, Alembik Y, Layet V, Afenjar A, Hannequin D, Demily C, Petit M, Thibaut F, Frebourg T, Campion D.
    Hum Mol Genet; 2007 Jan 01; 16(1):83-91. PubMed ID: 17135275
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  • 4. Early neurological phenotype in 4 children with biallelic PRODH mutations.
    Afenjar A, Moutard ML, Doummar D, Guët A, Rabier D, Vermersch AI, Mignot C, Burglen L, Heron D, Thioulouse E, de Villemeur TB, Campion D, Rodriguez D.
    Brain Dev; 2007 Oct 01; 29(9):547-52. PubMed ID: 17412540
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  • 5. The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD.
    Richard AC, Rovelet-Lecrux A, Delaby E, Charbonnier C, Thiruvahindrapuram B, Hatchwell E, Eis PS, Afenjar A, Gilbert Dussardier B, Scherer SW, Betancur C, Campion D.
    Am J Med Genet B Neuropsychiatr Genet; 2016 Apr 01; 171B(3):377-82. PubMed ID: 26978485
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  • 7. Inborn errors of proline metabolism.
    Mitsubuchi H, Nakamura K, Matsumoto S, Endo F.
    J Nutr; 2008 Oct 01; 138(10):2016S-2020S. PubMed ID: 18806117
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  • 8. [Type I Hyperprolinemia - What about the Kidney?].
    Rizzo M, Amicone M, Sellitti ML, Marino A, Sannino A, Capuano I, Pisani A.
    G Ital Nefrol; 2023 Dec 22; 40(6):. PubMed ID: 38156540
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  • 9. Biochemical and clinical features of hereditary hyperprolinemia.
    Mitsubuchi H, Nakamura K, Matsumoto S, Endo F.
    Pediatr Int; 2014 Aug 22; 56(4):492-6. PubMed ID: 24931297
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  • 10. Functional consequences of PRODH missense mutations.
    Bender HU, Almashanu S, Steel G, Hu CA, Lin WW, Willis A, Pulver A, Valle D.
    Am J Hum Genet; 2005 Mar 22; 76(3):409-20. PubMed ID: 15662599
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  • 11. Vitamin D insufficiency and schizophrenia risk: evaluation of hyperprolinemia as a mediator of association.
    Clelland JD, Read LL, Drouet V, Kaon A, Kelly A, Duff KE, Nadrich RH, Rajparia A, Clelland CL.
    Schizophr Res; 2014 Jun 22; 156(1):15-22. PubMed ID: 24787057
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  • 12. [Hyperprolinemia type Ⅰ caused by PRODH gene variation: 2 cases report and literature review].
    Xie ZH, Li X, Xiao MJ, Liu J, Zhang Q, Zhang ZK, Yang YL, Wang HJ, Chen YX, Zhang YD, Li DX.
    Zhonghua Er Ke Za Zhi; 2023 Oct 02; 61(10):935-937. PubMed ID: 37803864
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  • 14. Familial hyperprolinemia without mental retardation and hereditary nephropathy.
    Mollica F, Pavone L, Antener I.
    Monogr Hum Genet; 1972 Oct 02; 6():144-5. PubMed ID: 4663888
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  • 15. PRODH mutations and hyperprolinemia in a subset of schizophrenic patients.
    Jacquet H, Raux G, Thibaut F, Hecketsweiler B, Houy E, Demilly C, Haouzir S, Allio G, Fouldrin G, Drouin V, Bou J, Petit M, Campion D, Frébourg T.
    Hum Mol Genet; 2002 Sep 15; 11(19):2243-9. PubMed ID: 12217952
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  • 17. Hyperprolinemia is not associated with childhood onset schizophrenia.
    Jacquet H, Rapoport JL, Hecketsweiler B, Bobb A, Thibaut F, Frébourg T, Campion D.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Mar 05; 141B(2):192. PubMed ID: 16389584
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  • 19. Long-term neuropsychiatric follow-up in hyperprolinemia type I.
    Di Rosa G, Nicotera AG, Lenzo P, Spanò M, Tortorella G.
    Psychiatr Genet; 2014 Aug 05; 24(4):172-5. PubMed ID: 24842239
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