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Items: 20

1.

Monilethrix treated with minoxidil.

Rossi A, Iorio A, Scali E, Fortuna MC, Mari E, Palese E, Greco P, Carlesimo M.

Int J Immunopathol Pharmacol. 2011 Jan-Mar;24(1):239-42.

PMID:
21496408
2.

A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance.

De Cruz R, Horev L, Green J, Babay S, Sladden M, Zlotogorski A, Sinclair R.

Br J Dermatol. 2012 Jun;166 Suppl 2:20-6. doi: 10.1111/j.1365-2133.2012.10861.x.

PMID:
22670615
3.

Monilethrix: A New Family with the Novel Mutation in KRT81 Gene.

Ferrando J, Galve J, Torres-Puente M, Santillán S, Nogués S, Grimalt R.

Int J Trichology. 2012 Jan;4(1):53-5. doi: 10.4103/0974-7753.96105. No abstract available.

4.

Monilethrix.

de Lencastre A, Tosti A.

J Pediatr. 2012 Dec;161(6):1176. doi: 10.1016/j.jpeds.2012.06.033. Epub 2012 Aug 9. No abstract available.

PMID:
22884362
5.

A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene.

Farooq M, Ito M, Naito M, Shimomura Y.

Br J Dermatol. 2011 Aug;165(2):425-31. doi: 10.1111/j.1365-2133.2011.10373.x. Epub 2011 Jul 19.

PMID:
21495994
6.

Monilethrix in pattern distribution in siblings: diagnosis by trichoscopy.

Jain N, Khopkar U.

Int J Trichology. 2010 Jan;2(1):56-9. doi: 10.4103/0974-7753.66918.

7.

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix.

Winter H, Rogers MA, Langbein L, Stevens HP, Leigh IM, Labrèze C, Roul S, Taieb A, Krieg T, Schweizer J.

Nat Genet. 1997 Aug;16(4):372-4.

PMID:
9241275
8.

Monilethrix: improvement with acitretin.

Karincaoglu Y, Coskun BK, Seyhan ME, Bayram N.

Am J Clin Dermatol. 2005;6(6):407-10.

PMID:
16343029
9.

Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions.

Schaffer JV, Bazzi H, Vitebsky A, Witkiewicz A, Kovich OI, Kamino H, Shapiro LS, Amin SP, Orlow SJ, Christiano AM.

J Invest Dermatol. 2006 Jun;126(6):1286-91.

10.

An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis.

Zlotogorski A, Marek D, Horev L, Abu A, Ben-Amitai D, Gerad L, Ingber A, Frydman M, Reznik-Wolf H, Vardy DA, Pras E.

J Invest Dermatol. 2006 Jun;126(6):1292-6.

11.

Congenital monilethrix and hereditary unilateral external auditory canal atresia are co-inherited in a Chinese pedigree with recurrent KRT86 mutation.

Feng YG, Xiao SX, Xu AL, Feng JY, Wang JM.

J Dermatol. 2012 Sep;39(9):817-9. doi: 10.1111/j.1346-8138.2012.01565.x. Epub 2012 May 9. No abstract available.

PMID:
22568869
12.

Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis.

Shimomura Y, Sakamoto F, Kariya N, Matsunaga K, Ito M.

J Invest Dermatol. 2006 Jun;126(6):1281-5.

13.
14.

Keratosis pilaris and hereditary koilonychia without monilethrix.

Thai KE, Sinclair RD.

J Am Acad Dermatol. 2001 Oct;45(4):627-9.

PMID:
11568761
15.

Dermoscopy as a tool for rapid diagnosis of monilethrix.

Rakowska A, Slowinska M, Czuwara J, Olszewska M, Rudnicka L.

J Drugs Dermatol. 2007 Feb;6(2):222-4.

PMID:
17373184
16.

Review and new case reports on scanning electron microscopy of pili annulati, Monilethrix and Trichothiodystrophy.

Meyvisch K, Song M, Dourov N.

Scanning Microsc. 1992 Jun;6(2):537-41. Review.

PMID:
1462138
17.

Masquerading of trichotillomania in a family with monilethrix.

Neila Iglesias J, Rodríguez Pichardo A, García Bravo B, Camacho Martínez F.

Eur J Dermatol. 2011 Jan-Feb;21(1):133. doi: 10.1684/ejd.2010.1194. No abstract available.

PMID:
21224181
18.

A missense mutation in the type II hair keratin hHb3 is associated with monilethrix.

van Steensel MA, Steijlen PM, Bladergroen RS, Vermeer M, van Geel M.

J Med Genet. 2005 Mar;42(3):e19. No abstract available.

19.

Monilethrix: one step more on the ladder of cytogenetics.

Singh A, Ambujam S, Srikanth S, Uma A.

Int J Trichology. 2010 Jan;2(1):18-9. doi: 10.4103/0974-7753.66907.

20.

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