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Journal Abstract Search


186 related items for PubMed ID: 16531799

  • 1. Alpha1-antitrypsin gene polymorphisms are not associated with renal arterial fibromuscular dysplasia.
    Perdu J, Gimenez-Roqueplo AP, Boutouyrie P, Beaujour S, Laloux B, Nau V, Fiquet-Kempf B, Emmerich J, Tichet J, Plouin PF, Laurent S, Jeunemaitre X.
    J Hypertens; 2006 Apr; 24(4):705-10. PubMed ID: 16531799
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  • 2. Inheritance of arterial lesions in renal fibromuscular dysplasia.
    Perdu J, Boutouyrie P, Bourgain C, Stern N, Laloux B, Bozec E, Azizi M, Bonaiti-Pellié C, Plouin PF, Laurent S, Gimenez-Roqueplo AP, Jeunemaitre X.
    J Hum Hypertens; 2007 May; 21(5):393-400. PubMed ID: 17330059
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  • 3. Art, alpha-1-antitrypsin polymorphisms and intense creative energy: blessing or curse?
    Schmechel DE.
    Neurotoxicology; 2007 Sep; 28(5):899-914. PubMed ID: 17659342
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  • 4. [Alpha 1 antitrypsin polymorphism associated to asthma and emphysema in a central Tunisian population].
    Haj-Khelil A, Denden S, Hlioui L, Hattab N, Daimi H, Leban N, Perrin P, Lefranc G, Ben Chibani J.
    Ann Biol Clin (Paris); 2008 Sep; 66(4):379-84. PubMed ID: 18725338
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  • 5. Polymorphisms of the renin-angiotensin system in patients with multifocal renal arterial fibromuscular dysplasia.
    Bofinger A, Hawley C, Fisher P, Daunt N, Stowasser M, Gordon R.
    J Hum Hypertens; 2001 Mar; 15(3):185-90. PubMed ID: 11317203
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  • 6. Alpha-antitrypsin genotypes in Korean patients with chronic obstructive pulmonary disease.
    Kim CH, Yim JJ, Yoo CG, Lee CT, Kim YW, Han SK, Shim YS.
    Respirology; 2005 Mar; 10(2):223-8. PubMed ID: 15823189
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  • 7. A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software.
    Zaimidou S, van Baal S, Smith TD, Mitropoulos K, Ljujic M, Radojkovic D, Cotton RG, Patrinos GP.
    Hum Mutat; 2009 Mar; 30(3):308-13. PubMed ID: 19021233
    [Abstract] [Full Text] [Related]

  • 8. Fibromuscular dysplasia of the internal carotid artery associated with alpha1-antitrypsin deficiency.
    Schievink WI, Meyer FB, Parisi JE, Wijdicks EF.
    Neurosurgery; 1998 Aug; 43(2):229-33; discussion 233-4. PubMed ID: 9696074
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  • 10. Screening for alpha1-antitrypsin deficiency in Lithuanian patients with COPD.
    Sitkauskiene B, Serapinas D, Blanco I, Fernández-Bustillo E, Janciauskiene S, Sakalauskas R.
    Respir Med; 2008 Nov; 102(11):1654-8. PubMed ID: 18722101
    [Abstract] [Full Text] [Related]

  • 11. Alpha 1 antitrypsin polymorphism in the Tunisian population with special reference to pulmonary disease.
    Denden S, Haj Khelil A, Perrin P, Daimi H, Leban N, Ouaja A, Mahdouani K, Hlioui L, Lefranc G, Ben Chibani J.
    Pathol Biol (Paris); 2008 May; 56(3):106-10. PubMed ID: 18031952
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  • 12. Alpha 1-antitrypsin mutations in NAFLD: high prevalence and association with altered iron metabolism but not with liver damage.
    Valenti L, Dongiovanni P, Piperno A, Fracanzani AL, Maggioni M, Rametta R, Loria P, Casiraghi MA, Suigo E, Ceriani R, Remondini E, Trombini P, Fargion S.
    Hepatology; 2006 Oct; 44(4):857-64. PubMed ID: 17006922
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  • 18. [Study of the frequency of different phenotypes of alpha-1-antitrypsin in a population of Barcelona].
    Vidal R, Miravitlles M, Jardí R, Torrella M, Rodríguez-Frías F, Moral P, Vaqué J.
    Med Clin (Barc); 1996 Jul 06; 107(6):211-4. PubMed ID: 8755448
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  • 19. The prevalence of alpha(1)-antitrypsin deficiency in a representative population sample from Poland.
    Kaczor MP, Sanak M, Libura-Twardowska M, Szczeklik A.
    Respir Med; 2007 Dec 06; 101(12):2520-5. PubMed ID: 17693072
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