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Items: 1 to 20 of 232

1.

Achalasia of the cardia in Allgrove's (triple A) syndrome: histopathologic study of 10 cases.

Khelif K, De Laet MH, Chaouachi B, Segers V, Vanderwinden JM.

Am J Surg Pathol. 2003 May;27(5):667-72.

PMID:
12717251
2.

Two siblings with Allgrove's syndrome and extrapyramidal features.

Jacob A, Parameswaran K, Kishore A.

Neurol India. 2003 Jun;51(2):257-9.

3.

Mutations of the AAAS gene in an Indian family with Allgrove's syndrome.

Mukhopadhya A, Danda S, Huebner A, Chacko A.

World J Gastroenterol. 2006 Aug 7;12(29):4764-6.

4.

Allgrove or 4 "A" syndrome: an autosomal recessive syndrome causing multisystem neurological disease.

Kimber J, McLean BN, Prevett M, Hammans SR.

J Neurol Neurosurg Psychiatry. 2003 May;74(5):654-7.

5.

[Achalasia, alacrima without adrenal insufficiency with peripheral and autonomic neurological dysfunction (Allgrove's syndrome)].

García-Compeán D, Ramón Martínez H, Villegas-González MJ, Montes J, García Quintanilla F, González JA.

Rev Gastroenterol Mex. 1998 Jan-Mar;63(1):33-6. Spanish.

PMID:
10068747
6.

[Childhood achalasia: a separate entity?].

Bohl J, Gockel I, Sultanov F, Eckardt V, Junginger T.

Z Gastroenterol. 2007 Dec;45(12):1273-80. Review. German.

PMID:
18080230
7.

Achalasia-alacrima-ACTH insensitivity syndrome (Triple-A-syndrome).

Dugardeyn C, Anooshiravani M, Christophe C, Goyens P, Perlmutter N.

J Belge Radiol. 1993 Jun;76(3):167-8.

PMID:
8253654
8.

[Allgrove's syndrome].

Chiheb S, Slaoui Z, Nejjam F, Habibeddine S, Lakhdar H.

Ann Dermatol Venereol. 2001 Oct;128(10 Pt 1):1043-5. French.

PMID:
11907967
9.

The "Double A" phenotype: Portending Allgrove's syndrome and averting adrenal crisis.

Goswami S, Roy A, Bhattacharjee R, Shivaprasad KS, Chakraborty PP, Selvan C, Thukral A, Biswas K, Ghosh S, Mukhopadhyay S, Chowdhury S.

Indian J Endocrinol Metab. 2012 Dec;16(Suppl 2):S367-8. doi: 10.4103/2230-8210.104095.

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 30;146(48):2295-7. Review. Dutch.

PMID:
12497758
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.

PMID:
1850671
13.

Congenital achalasia: facts and fantasies.

Zilberstein B, de Cleva R, Gabriel AG, Neto SG, Gama-Rodrigues JJ.

Dis Esophagus. 2005;18(5):335-7.

PMID:
16197535
14.

Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster.

Weber A, Wienker TF, Jung M, Easton D, Dean HJ, Heinrichs C, Reis A, Clark AJ.

Hum Mol Genet. 1996 Dec;5(12):2061-6.

15.

Triple-A syndrome.

Sarathi V, Shah NS.

Adv Exp Med Biol. 2010;685:1-8. Review.

PMID:
20687490
16.

Analysis of the AAAS gene in a Japanese patient with triple A syndrome.

Katsumata N, Hirose H, Kagami M, Tanaka T.

Endocr J. 2002 Feb;49(1):49-53.

17.

[Allgrove syndrome (achalasia-alacrima-adrenal gland insufficiency): report of a case].

Chávez M, Moreno C, Pérez A, García F, Sólis J, Cargone A, Astete M, Contardo C.

Rev Gastroenterol Peru. 1996 May-Aug;16(2):153-7. Spanish.

PMID:
8924656
18.

The nature of the myenteric infiltrate in achalasia: an immunohistochemical analysis.

Clark SB, Rice TW, Tubbs RR, Richter JE, Goldblum JR.

Am J Surg Pathol. 2000 Aug;24(8):1153-8.

PMID:
10935657
19.

Pediatric alacrima, achalasia, and mental retardation.

Ornek K, Atilla H, Zilelioğlu G.

J AAPOS. 2002 Aug;6(4):261-3.

PMID:
12185357
20.

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. doi: 10.1080/13816810802502962.

PMID:
19172511
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