Format
Sort by

Send to

Choose Destination

Selected items

Items: 20

1.

Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2.

Aten E, Brasz LC, Bornholdt D, Hooijkaas IB, Porteous ME, Sybert VP, Vermeer MH, Vossen RH, van der Wielen MJ, Bakker E, Breuning MH, Grzeschik KH, Oosterwijk JC, den Dunnen JT.

Hum Mutat. 2010 Oct;31(10):1125-33. doi: 10.1002/humu.21335.

PMID:
20672378
2.

Cyclooxygenase-2 inhibition restores ultraviolet B-induced downregulation of ATP2A2/SERCA2 in keratinocytes: possible therapeutic approach of cyclooxygenase-2 inhibition for treatment of Darier disease.

Kamijo M, Nishiyama C, Takagi A, Nakano N, Hara M, Ikeda S, Okumura K, Ogawa H.

Br J Dermatol. 2012 May;166(5):1017-22. doi: 10.1111/j.1365-2133.2011.10789.x.

PMID:
22413864
3.

Darier disease : a disease model of impaired calcium homeostasis in the skin.

Savignac M, Edir A, Simon M, Hovnanian A.

Biochim Biophys Acta. 2011 May;1813(5):1111-7. doi: 10.1016/j.bbamcr.2010.12.006. Review.

4.

Protein aggregation of SERCA2 mutants associated with Darier disease elicits ER stress and apoptosis in keratinocytes.

Wang Y, Bruce AT, Tu C, Ma K, Zeng L, Zheng P, Liu Y, Liu Y.

J Cell Sci. 2011 Nov 1;124(Pt 21):3568-80. doi: 10.1242/jcs.084053.

5.

[Darier-White disease treated with oral isotretinoin].

Eimer L, Lagodin C, Bonavia P, Stringa M, Rébora I, Anaya J.

Arch Argent Pediatr. 2011 Aug;109(4):e63-6. doi: 10.1590/S0325-00752011000400014. Spanish.

6.

Darier-White disease: a review of the clinical features in 163 patients.

Burge SM, Wilkinson JD.

J Am Acad Dermatol. 1992 Jul;27(1):40-50. Review.

PMID:
1619075
7.

Local hyperthermia treatment of extensive viral warts in Darier disease: a case report and literature review.

Li X, Zhang C, Hong Y, Zhang D, Wei H, Chen HD, Gao XH.

Int J Hyperthermia. 2012;28(5):451-5. doi: 10.3109/02656736.2012.677929.

PMID:
22690793
8.

Keratosis follicularis spinulosa decalvans in a female.

Sequeira FF, Jayaseelan E.

Indian J Dermatol Venereol Leprol. 2011 May-Jun;77(3):325-7. doi: 10.4103/0378-6323.79708.

9.

MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvans.

Fong K, Wedgeworth EK, Lai-Cheong JE, Tosi I, Mellerio JE, Powell AM, McGrath JA.

Clin Exp Dermatol. 2012 Aug;37(6):631-4. doi: 10.1111/j.1365-2230.2011.04288.x.

PMID:
22816986
10.

Darier disease with oral and esophageal involvement: a case report.

Thiagarajan MK, Narasimhan M, Sankarasubramanian A.

Indian J Dent Res. 2011 Nov-Dec;22(6):843-6. doi: 10.4103/0970-9290.94682.

11.

[Successful treatment of Darier disease with oral alitretinoin].

Barnstedt SE.

Hautarzt. 2012 Feb;63(2):139-41. doi: 10.1007/s00105-011-2207-9. German.

PMID:
21761212
12.

The neuropsychiatric phenotype in Darier disease.

Gordon-Smith K, Jones LA, Burge SM, Munro CS, Tavadia S, Craddock N.

Br J Dermatol. 2010 Sep;163(3):515-22. doi: 10.1111/j.1365-2133.2010.09834.x.

PMID:
20456342
13.

Familial erythromelanosis follicularis faciei et colli with extensive keratosis pilaris.

Lalit G, Anubhav G, Kumar KA, Asit M.

Int J Dermatol. 2011 Nov;50(11):1400-1. doi: 10.1111/j.1365-4632.2010.04776.x. No abstract available.

PMID:
22004497
14.

Bullous-hemorrhagic Darier disease.

Sánchez-Salas MP, Latasa de Aranibar FJ, Oncíns Torres R, Gambó Grasa P.

Skinmed. 2011 Jan-Feb;9(1):65-6.

PMID:
21409967
15.

Molecular characterization of 11 Italian patients with Darier disease.

Pedace L, Barboni L, Pozzetto E, Amantea A, Zambruno G, Preziosi N, Benedicenti F, Boni S, De Brasi D, Panetta C, Ferraro C, De Bernardo C, Castori M, Grammatico P.

Eur J Dermatol. 2011 May-Jun;21(3):334-8. doi: 10.1684/ejd.2011.1339.

PMID:
21527373
16.

Novel splice-site and frameshift ATP2A2 mutations in Chinese patients with Darier disease.

Shi HJ, Li M, Zhang GL, Xu SX, Shao MH, Gu Y, Du XF, Mu HJ, Xie P.

Clin Exp Dermatol. 2012 Aug;37(6):677-9. doi: 10.1111/j.1365-2230.2011.04311.x. No abstract available.

PMID:
22329366
17.

Keratosis follicularis spinulosa decalvans in a family.

Bellet JS, Kaplan AL, Selim MA, Olsen EA.

J Am Acad Dermatol. 2008 Mar;58(3):499-502. doi: 10.1016/j.jaad.2007.03.028.

PMID:
18280351
18.

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease.

Sakuntabhai A, Ruiz-Perez V, Carter S, Jacobsen N, Burge S, Monk S, Smith M, Munro CS, O'Donovan M, Craddock N, Kucherlapati R, Rees JL, Owen M, Lathrop GM, Monaco AP, Strachan T, Hovnanian A.

Nat Genet. 1999 Mar;21(3):271-7.

PMID:
10080178
19.

Acrokeratosis verruciformis of Hopf showing P602L mutation in ATP2A2 and overlapping histopathological features with Darier disease.

Bergman R, Sezin T, Indelman M, Helou WA, Avitan-Hersh E.

Am J Dermatopathol. 2012 Aug;34(6):597-601. doi: 10.1097/DAD.0b013e31823f9194.

PMID:
22814319
20.

Erythromelanosis follicularis faciei et colli: relationship with keratosis pilaris.

Augustine M, Jayaseelan E.

Indian J Dermatol Venereol Leprol. 2008 Jan-Feb;74(1):47-9.

Items per page

Supplemental Content

Support Center