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Items: 1 to 20 of 288

1.

Cutaneous manifestations of Costello syndrome.

Nguyen V, Buka RL, Roberts BJ, Eichenfield LF.

Int J Dermatol. 2007 Jan;46(1):72-6.

PMID:
17214726
2.

Costello syndrome.

Madhukara J, Kumaran MS.

Indian J Dermatol Venereol Leprol. 2007 Nov-Dec;73(6):406-8.

3.

Further delineation of Costello syndrome.

Teebi AS, Shaabani IS.

Am J Med Genet. 1993 Aug 15;47(2):166-8. Review.

PMID:
8213898
4.
5.

Costello syndrome: report and review.

van Eeghen AM, van Gelderen I, Hennekam RC.

Am J Med Genet. 1999 Jan 15;82(2):187-93. Review.

PMID:
9934987
6.

Delineation of the Costello syndrome.

Martin RA, Jones KL.

Am J Med Genet. 1991 Dec 1;41(3):346-9.

PMID:
1789291
7.

Costello syndrome with decreased glucose tolerance.

Szalai S, Becker K, Török E.

Eur J Dermatol. 1999 Oct-Nov;9(7):533-6.

PMID:
10523730
8.

The Costello syndrome: report of a case and review of the literature.

Kondo I, Tamanaha K, Ashimine K.

Jpn J Hum Genet. 1993 Dec;38(4):433-6. Review.

PMID:
7514457
9.

[Syringoma and trisomy 21].

Thomas L, Chamchikh N, Audefray D, Moulin G.

Ann Dermatol Venereol. 1993;120(10):689-91. French.

PMID:
8161099
10.

Costello syndrome showing moyamoya-like vasculopathy.

Shiihara T, Kato M, Mitsuhashi Y, Hayasaka K.

Pediatr Neurol. 2005 May;32(5):361-3.

PMID:
15866441
11.

Myocardial storage of chondroitin sulfate-containing moieties in Costello syndrome patients with severe hypertrophic cardiomyopathy.

Hinek A, Teitell MA, Schoyer L, Allen W, Gripp KW, Hamilton R, Weksberg R, Klüppel M, Lin AE.

Am J Med Genet A. 2005 Feb 15;133A(1):1-12.

PMID:
15637729
12.

Eruptive syringoma in a patient with trisomy 21.

Ong GC, Lim KS, Chian LY.

Singapore Med J. 2010 Feb;51(2):e46-7.

13.

Perforating milia-like idiopathic calcinosis cutis and periorbital syringomas in a girl with Down syndrome.

Schepis C, Siragusa M, Palazzo R, Batolo D, Romano C.

Pediatr Dermatol. 1994 Sep;11(3):258-60.

PMID:
7971561
14.

Further evidence of genetic heterogeneity in Costello syndrome: involvement of the KRAS gene.

Bertola DR, Pereira AC, Brasil AS, Albano LM, Kim CA, Krieger JE.

J Hum Genet. 2007;52(6):521-6. Epub 2007 Apr 28.

PMID:
17468812
15.

Del(2q)--cause of the wrinkly skin syndrome?

Kreuz FR, Wittwer BH.

Clin Genet. 1993 Mar;43(3):132-8. Review.

PMID:
8500259
16.

Wrinkly skin syndrome: phenotype and additional manifestations.

Casamassima AC, Wesson SK, Conlon CJ, Weiss FH.

Am J Med Genet. 1987 Aug;27(4):885-93. Review.

PMID:
3321993
17.

Familial syringoma: report of two cases with a published work review and the unique association with steatocystoma multiplex.

Marzano AV, Fiorani R, Girgenti V, Crosti C, Alessi E.

J Dermatol. 2009 Mar;36(3):154-8. doi: 10.1111/j.1346-8138.2009.00613.x. Review.

PMID:
19335690
18.

The Costello syndrome: a boy with thick mitral valves and arrhythmias.

Izumikawa Y, Naritomi K, Tohma T, Shiroma N, Hirayama K.

Jpn J Hum Genet. 1993 Sep;38(3):329-34. Review.

PMID:
7505126
19.

Elastic fiber degeneration in Costello syndrome.

Mori M, Yamagata T, Mori Y, Nokubi M, Saito K, Fukushima Y, Momoi MY.

Am J Med Genet. 1996 Feb 2;61(4):304-9.

PMID:
8834040
20.

Costello syndrome in two Brazilian children.

Pratesi R, Santos M, Ferrari I.

J Med Genet. 1998 Jan;35(1):54-7. Review.

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