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Items: 6

1.

Tietz syndrome: unique phenotype specific to mutations of MITF nuclear localization signal.

Izumi K, Kohta T, Kimura Y, Ishida S, Takahashi T, Ishiko A, Kosaki K.

Clin Genet. 2008 Jul;74(1):93-5. doi: 10.1111/j.1399-0004.2008.01010.x. Epub 2008 May 28. No abstract available.

PMID:
18510545
2.

Microphthalmia-associated transcription factor (MITF): multiplicity in structure, function, and regulation.

Shibahara S, Takeda K, Yasumoto K, Udono T, Watanabe K, Saito H, Takahashi K.

J Investig Dermatol Symp Proc. 2001 Nov;6(1):99-104. Review.

3.

Tietze's syndrome. A bridge between neurocirculatory asthenia and mitral valve prolapse syndrome.

Halle S.

J La State Med Soc. 1984 Mar;136(3):20-1. Review. No abstract available.

PMID:
6373985
4.

[ETIOPATHOGENESIS OF TIETZE'S CHONDROPATHY].

PEROSA L, MANGANELLI G.

Recenti Prog Med. 1965 Feb;38:119-49. Review. Italian. No abstract available.

PMID:
14309877
5.

[Tietze's syndrome in the elderly: description of a case and review of the literature].

Martino G, Cariati S, Elmore U, Pascarella G, Corbelli GC, Hekmatdousttabrizi A, Carlomagno R.

G Chir. 1994 Mar;15(3):119-23. Review. Italian.

PMID:
8060778
6.

Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome).

Desir J, Abramowicz M.

Orphanet J Rare Dis. 2008 Oct 15;3:28. doi: 10.1186/1750-1172-3-28. Review.

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