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11. [From gene to disease; adrenocortical insufficiency, achalasia and disrupted tear secretion: Allgrove syndrome]. van Daele PL; de Herder WW; Huebner A Ned Tijdschr Geneeskd; 2002 Nov; 146(48):2295-7. PubMed ID: 12497758 [TBL] [Abstract][Full Text] [Related]
12. 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; 30(1):45-9. PubMed ID: 19172511 [TBL] [Abstract][Full Text] [Related]
14. Heterogeneity of the triple A syndrome and assessment of a case. Lovrecić L; Pelet A; Peterlin B Genet Couns; 2006; 17(2):191-5. PubMed ID: 16970037 [TBL] [Abstract][Full Text] [Related]
15. Familial achalasia associated with adrenocortical insufficiency, alacrima, and neurological abnormalities. Ehrich E; Aranoff G; Johnson WG Am J Med Genet; 1987 Mar; 26(3):637-44. PubMed ID: 3565479 [TBL] [Abstract][Full Text] [Related]
16. [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; 147(10):469-70; author reply 470. PubMed ID: 12666522 [No Abstract] [Full Text] [Related]
17. Allgrove syndrome: case report of 7 years old boy from Bahawalpur. Akram S; Khan MA; Rehman A J Pak Med Assoc; 2018 Aug; 68(8):1260-1262. PubMed ID: 30108399 [TBL] [Abstract][Full Text] [Related]
18. Allgrove syndrome--a syndrome of primary adrenocortical insufficiency with achalasia of the cardia and deficient tear production. Bhargavan PV; Kumar KM; Rajendran VR; Fassaludeen AS J Assoc Physicians India; 2003 Jul; 51():726-8. PubMed ID: 14621049 [TBL] [Abstract][Full Text] [Related]
19. Allgrove syndrome in a Mexican American family is caused by an ancestral mutation derived from North Africa. Chang AJ; Kline MM; Currie Y; Perez MO; Hartiala J; Wijesuriya H; Buchanan TA; Watanabe RM; Allayee H Clin Genet; 2008 Apr; 73(4):385-7. PubMed ID: 18261130 [No Abstract] [Full Text] [Related]
20. The diagnosis of adrenal insufficiency in a patient with Allgrove syndrome and a novel mutation in the ALADIN gene. Salehi M; Houlden H; Sheikh A; Poretsky L Metabolism; 2005 Feb; 54(2):200-5. PubMed ID: 15690314 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]