These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
93 related articles for article (PubMed ID: 2817011)
1. Three sibs with achalasia and alacrimia: a separate entity different from triple-A syndrome. Haverkamp F; Zerres K; Rosskamp R Am J Med Genet; 1989 Oct; 34(2):289-91. PubMed ID: 2817011 [TBL] [Abstract][Full Text] [Related]
2. Familial glucocorticoid deficiency, alacrimia and achalasia--Allgrove syndrome. Muranjan MN; Gurav M; Surve T; Deshmukh CT; Bharucha BA Indian J Pediatr; 1999; 66(1):151-4. PubMed ID: 10798051 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Four siblings with achalasia, alacrimia and neurological abnormalities in a consanguineous family. Kasirga E; Ozkinay F; Tütüncüoğlu S; Aydoğdu S; Colakoğlu Z; Musoğlu A; Yağci A; Taneli B; Yağci RV Clin Genet; 1996 Jun; 49(6):296-9. PubMed ID: 8884077 [TBL] [Abstract][Full Text] [Related]
5. Case report of a familial triple: a syndrome and review of the literature. Gaiani F; Gismondi P; Minelli R; Casadio G; de'Angelis N; Fornaroli F; de'Angelis GL; Manfredi M Medicine (Baltimore); 2020 May; 99(22):e20474. PubMed ID: 32481456 [TBL] [Abstract][Full Text] [Related]
6. Esophageal achalasia and alacrima in siblings. Singh A; Shah A Indian Pediatr; 2006 Feb; 43(2):161-3. PubMed ID: 16528113 [TBL] [Abstract][Full Text] [Related]
7. [Simultaneous occurrence of selective ACTH deficiency , achalasia, alacrimia and hyperlipoproteinemia]. Várkonyi A; Julesz J; Szüts P; Tóth I; Faredin I Orv Hetil; 1990 Dec; 131(50):2763-6. PubMed ID: 2176279 [TBL] [Abstract][Full Text] [Related]
8. A syndrome of alacrima, achalasia, and neurologic anomalies without adrenocortical insufficiency. el-Rayyes K; Hegab S; Besisso M J Pediatr Ophthalmol Strabismus; 1991; 28(1):35-7. PubMed ID: 2019957 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Oral manifestations of triple A syndrome. Vucicevic-Boras V; Juras D; Gruden-Pokupec JS; Vidovic A Eur J Med Res; 2003 Jul; 8(7):318-20. PubMed ID: 12911870 [TBL] [Abstract][Full Text] [Related]
11. Achalasia cardia and alacrima in an infant. Fayyaz A; Ali S J Coll Physicians Surg Pak; 2004 Jun; 14(6):368-9. PubMed ID: 15233895 [TBL] [Abstract][Full Text] [Related]
17. Achalasia and microcephaly. Dumars KW; Williams JJ; Steele-Sandlin C Am J Med Genet; 1980; 6(4):309-14. PubMed ID: 7211947 [TBL] [Abstract][Full Text] [Related]
18. 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 [TBL] [Abstract][Full Text] [Related]