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Journal Abstract Search

114 related items for PubMed ID: 26007668

  • 21. [On the pathogenesis of cardiospasm (esophageal achalasia) in children].
    Geras'kin VI, Lindenberg LK.
    Vopr Okhr Materin Det; 1967 Dec; 12(12):48-51. PubMed ID: 5612156
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  • 22. [Allgrove syndrome (triple A). Finding of a mutation not described in the AAAS gene].
    Capataz Ledesma M, Méndez Pérez P, Rodríguez López R, Galán Gómez E.
    An Pediatr (Barc); 2013 Feb; 78(2):109-12. PubMed ID: 22824007
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  • 25. Mutant WD-repeat protein in triple-A syndrome.
    Tullio-Pelet A, Salomon R, Hadj-Rabia S, Mugnier C, de Laet MH, Chaouachi B, Bakiri F, Brottier P, Cattolico L, Penet C, Bégeot M, Naville D, Nicolino M, Chaussain JL, Weissenbach J, Munnich A, Lyonnet S.
    Nat Genet; 2000 Nov; 26(3):332-5. PubMed ID: 11062474
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  • 26. Achalasia associated with squamous cell carcinoma of the esophagus: a case report.
    Rock LA, Latham PS, Hankins JR, Nasrallah SM.
    Am J Gastroenterol; 1985 Jul; 80(7):526-8. PubMed ID: 4014101
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  • 29. Genotypic heterogeneity and clinical phenotype in triple A syndrome: a review of the NIH experience 2000-2005.
    Brooks BP, Kleta R, Stuart C, Tuchman M, Jeong A, Stergiopoulos SG, Bei T, Bjornson B, Russell L, Chanoine JP, Tsagarakis S, Kalsner L, Stratakis C.
    Clin Genet; 2005 Sep; 68(3):215-21. PubMed ID: 16098009
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  • 32. [From gene to disease; adrenocortical insufficiency, achalasia and disrupted tear secretion: Allgrove syndrome].
    van Heerde M, Vulsma T, Schweizer JJ, Kneepkens CM, Delemarre-van der Waal HA.
    Ned Tijdschr Geneeskd; 2003 Mar 08; 147(10):469-70; author reply 470. PubMed ID: 12666522
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  • 33. Three children with triple A syndrome due to a mutation (R478X) in the AAAS gene.
    Yuksel B, Braun R, Topaloglu AK, Mungan NO, Ozer G, Huebner A.
    Horm Res; 2004 Mar 08; 61(1):3-6. PubMed ID: 14646395
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  • 34. Triple A or Allgrove syndrome. A case report with ophthalmic abnormalities and a novel mutation in the AAAS gene.
    Villanueva-Mendoza C, artínez-Guzmán O, Rivera-Parra D, Zenteno JC.
    Ophthalmic Genet; 2009 Mar 08; 30(1):45-9. PubMed ID: 19172511
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  • 38. Genetic separation of the human lacritin gene ("LACRT") and triple A (Allgrove) syndrome on 12q13.
    Kumar R, Huebner A, Laurie GW.
    Adv Exp Med Biol; 2002 Mar 08; 506(Pt A):167-74. PubMed ID: 12613904
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  • 39. Allgrove syndrome.
    Kilicli F, Acibucu F, Senel S, Dokmetas HS.
    Singapore Med J; 2012 May 08; 53(5):e92-4. PubMed ID: 22584989
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