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Items: 10

1.

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.

PMID:
8968764
2.

[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
3.

ACTH resistance syndromes.

Huebner A, Elias LL, Clark AJ.

J Pediatr Endocrinol Metab. 1999 Apr;12 Suppl 1:277-93. Review.

PMID:
10698592
4.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
5.

Triple-A syndrome.

Sarathi V, Shah NS.

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

PMID:
20687490
6.

Adult or late-onset triple A syndrome: case report and literature review.

Nakamura K, Yoshida K, Yoshinaga T, Kodaira M, Shimojima Y, Takei Y, Morita H, Kayanuma K, Ikeda S.

J Neurol Sci. 2010 Oct 15;297(1-2):85-8. doi: 10.1016/j.jns.2010.07.006. Review.

PMID:
20674935
7.

The human type II keratin gene cluster on chromosome 12q13.13: final count or hidden secrets?

Bowden PE.

J Invest Dermatol. 2005 Mar;124(3):xv-xvii. Review. No abstract available.

8.

[Achalasia, alacrimia and cortisol deficiency--Allgrove syndrome].

Hübschmann K.

Klin Padiatr. 1995 May-Jun;207(3):126-9. Review. German.

PMID:
7623430
9.

[ACTH resistance syndromes].

Naville D, Penhoat A, Bégeot M.

Ann Endocrinol (Paris). 2000 Nov;61(5):428-39. Review. French.

PMID:
11084394
10.

Synopsis of investigations into proposed theories on the etiology of achalasia.

Petersen RP, Martin AV, Pellegrini CA, Oelschlager BK.

Dis Esophagus. 2012 May;25(4):305-10. doi: 10.1111/j.1442-2050.2009.01030.x. Review.

PMID:
20002702

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