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Items: 1 to 20 of 197

1.

Darier's disease: epidemiology, pathophysiology, and management.

Cooper SM, Burge SM.

Am J Clin Dermatol. 2003;4(2):97-105. Review.

PMID:
12553850
2.

Management of Darier's disease.

Burge S.

Clin Exp Dermatol. 1999 Mar;24(2):53-6. Review.

PMID:
10233651
3.

Histological characterization of Darier's disease in Tunisian families.

Kassar S, Tounsi-Kettiti H, Charfeddine C, Zribi H, Bchetnia M, Jerbi E, Mokni M, Ben Osman A, Abdelhak S, Boubaker S.

J Eur Acad Dermatol Venereol. 2009 Oct;23(10):1178-83. doi: 10.1111/j.1468-3083.2009.03283.x. Epub 2009 May 26.

PMID:
19486234
4.

Identification a novel missense mutation p.R761L in Chinese patients with Darier's disease.

Song J, Li M, Yang LJ, Zhang GL.

Arch Dermatol Res. 2010 May;302(4):311-4. doi: 10.1007/s00403-010-1042-7. Epub 2010 Mar 5.

PMID:
20204653
5.

Darier's disease associated with bipolar affective disorder: a case report.

Wang SL, Yang SF, Chen CC, Tsai PT, Chai CY.

Kaohsiung J Med Sci. 2002 Dec;18(12):622-6.

PMID:
12670038
6.

Clinical case of acral hemorrhagic Darier's disease is not caused by mutations in exon 15 of the ATP2A2 gene.

Pećina-Slaus N, Milavec-Puretić V, Kubat M, Furac I, Karija M, Fischer-Zigmund M, Lipozencić J.

Coll Antropol. 2003 Jun;27(1):125-33.

PMID:
12974140
7.

A Japanese case of segmental Darier's disease caused by mosaicism for the ATP2A2 mutation.

Wada T, Shirakata Y, Takahashi H, Murakami S, Iizuka H, Suzuki H, Hashimoto K.

Br J Dermatol. 2003 Jul;149(1):185-8.

PMID:
12890216
8.

Seven novel mutations in the ATP2A2 gene of Austrian patients with Darier's disease.

Klausegger A, Nischler E, Wagner RN, Pletschacher F, Hintner H, Bauer JW.

Arch Dermatol Res. 2011 Jul;303(5):371-4. doi: 10.1007/s00403-011-1148-6. Epub 2011 Apr 26.

PMID:
21519848
9.

Localized Darier's disease in a Blaschkoid distribution: two cases of phenotypic mosaicism and a review of mosaic Darier's disease.

Sanderson EA, Killoran CE, Pedvis-Leftick A, Wilkel CS.

J Dermatol. 2007 Nov;34(11):761-4. Review.

PMID:
17973816
10.

[Improvement of Darier's disease on treatment with topical 5-fluorouracil].

Velasco S, Guillet G.

Ann Dermatol Venereol. 2006 Apr;133(4):366-8. French.

PMID:
16733453
11.

Dyskeratosis follicularis disease: case reports and review of the literature.

Zeglaoui F, Zaraa I, Fazaa B, Houimli S, El Fekih N, Ezzine N, Kamoun MR.

J Eur Acad Dermatol Venereol. 2005 Jan;19(1):114-7. Review.

PMID:
15649206
12.

[Possible genetic link between Darier's disease and depression. Review of the literature and case history].

Bach DR, Moggi F, Müller TJ, Seifritz E, Strik WK, Wirtz G.

Nervenarzt. 2007 Jan;78(1):81-4. Review. German.

PMID:
16786359
13.

ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes.

Jacobsen NJ, Lyons I, Hoogendoorn B, Burge S, Kwok PY, O'Donovan MC, Craddock N, Owen MJ.

Hum Mol Genet. 1999 Sep;8(9):1631-6.

PMID:
10441325
14.

Darier's disease: a commonly misdiagnosed cutaneous disorder.

Chacon GR, Wolfson DJ, Palacio C, Sinha AA.

J Drugs Dermatol. 2008 Apr;7(4):387-90.

PMID:
18459521
15.

Mosaicism for ATP2A2 mutations causes segmental Darier's disease.

Sakuntabhai A, Dhitavat J, Burge S, Hovnanian A.

J Invest Dermatol. 2000 Dec;115(6):1144-7.

16.

[Efficacy and risks of topical 5-fluorouracil in Darier's disease].

Le Bidre E, Delage M, Celerier P, De Muret A, Lorette G.

Ann Dermatol Venereol. 2010 Jun-Jul;137(6-7):455-9. doi: 10.1016/j.annder.2010.04.002. Epub 2010 May 20. French.

PMID:
20620575
17.

Spectrum of novel ATP2A2 mutations in patients with Darier's disease.

Sakuntabhai A, Burge S, Monk S, Hovnanian A.

Hum Mol Genet. 1999 Sep;8(9):1611-9.

PMID:
10441323
18.

New mutations of Darier disease in Tunisian patients.

Bchetnia M, Benmously R, Ben Brick AS, Charfeddine C, Ben Ameur Y, Fajraoui M, Debbiche A, Ben Ayed M, Mokni M, Fenniche S, Mokhtar I, Abdelhak S.

Arch Dermatol Res. 2009 Sep;301(8):615-9. doi: 10.1007/s00403-009-0963-5. Epub 2009 Jun 2.

PMID:
19488774
19.

ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class.

Ruiz-Perez VL, Carter SA, Healy E, Todd C, Rees JL, Steijlen PM, Carmichael AJ, Lewis HM, Hohl D, Itin P, Vahlquist A, Gobello T, Mazzanti C, Reggazini R, Nagy G, Munro CS, Strachan T.

Hum Mol Genet. 1999 Sep;8(9):1621-30.

PMID:
10441324
20.

Loss of function mutations in ATP2A2 and psychoses: A case report and literature survey.

Nakamura T, Kazuno AA, Nakajima K, Kusumi I, Tsuboi T, Kato T.

Psychiatry Clin Neurosci. 2016 Aug;70(8):342-50. doi: 10.1111/pcn.12395. Epub 2016 Jun 3.

PMID:
27106560

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