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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 2019957)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. [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]  

  • 5. 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]  

  • 6. [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]  

  • 7. Pediatric alacrima, achalasia, and mental retardation.
    Ornek K; Atilla H; Zilelioğlu G
    J AAPOS; 2002 Aug; 6(4):261-3. PubMed ID: 12185357
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A broad range of symptoms in allgrove syndrome: single center experience in Southeast Anatolia.
    Polat R; Ustyol A; Tuncez E; Guran T
    J Endocrinol Invest; 2020 Feb; 43(2):185-196. PubMed ID: 31435881
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Familial hypoglycocorticism syndrome unresponsive to ACTH, achalasia, alacrima, with associated distal neuromyopathy].
    Degli Esposti A; Ambrosioni G; Giardina A; Giovannini G; Laghi MG; Molinari PP; Salvatori P; Zaniboni MG
    Minerva Pediatr; 1985 May; 37(9):353-9. PubMed ID: 2993839
    [No Abstract]   [Full Text] [Related]  

  • 11. AAA syndrome--adrenal insufficiency, alacrima and achalasia.
    Wallace IR; Hunter SJ
    QJM; 2012 Aug; 105(8):803-4. PubMed ID: 21865313
    [No Abstract]   [Full Text] [Related]  

  • 12. Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima.
    Moore PS; Couch RM; Perry YS; Shuckett EP; Winter JS
    Clin Endocrinol (Oxf); 1991 Feb; 34(2):107-14. PubMed ID: 1850671
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Selective ACTH insensitivity, achalasia, and alacrima: a multisystem disorder presenting in childhood.
    Geffner ME; Lippe BM; Kaplan SA; Berquist WE; Bateman JB; Paterno VI; Seegan R
    Pediatr Res; 1983 Jul; 17(7):532-6. PubMed ID: 6312400
    [No Abstract]   [Full Text] [Related]  

  • 17. [Allgrove's syndrome].
    Chiheb S; Slaoui Z; Nejjam F; Habibeddine S; Lakhdar H
    Ann Dermatol Venereol; 2001 Oct; 128(10 Pt 1):1043-5. PubMed ID: 11907967
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spinal cord atrophy in triple A syndrome associated with a novel compound heterozygous mutation.
    Kunte H; Trendelenburg G; Matzen J; Ventz M; Kornak U; Harms L
    Neuro Endocrinol Lett; 2010; 31(3):301-3. PubMed ID: 20588230
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 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]
    of 8.