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Results: 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
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
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.

PMID:
22628999
[PubMed]
Free PMC Article
4.

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.

PMID:
21188029
[PubMed]
Free PMC Article
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
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

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.

PMID:
16575393
[PubMed - indexed for MEDLINE]
Free Article
8.

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.

PMID:
16543896
[PubMed - indexed for MEDLINE]
Free Article
9.

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.

PMID:
16439973
[PubMed - indexed for MEDLINE]
Free Article
10.

Monilethrix: improvement with acitretin.

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

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

PMID:
16343029
[PubMed - indexed for MEDLINE]
11.

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
[PubMed - indexed for MEDLINE]
12.

Severe monilethrix associated with intractable scalp pruritus, posterior subcapsular cataract, brachiocephaly, and distinct facial features: a new variant of monilethrix syndrome?

Erbagci Z, Erbagci I, Erbagci H, Erkilic S, Tuncel AA.

Pediatr Dermatol. 2004 Jul-Aug;21(4):486-90.

PMID:
15283798
[PubMed - indexed for MEDLINE]
13.

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
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
16.

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
[PubMed - indexed for MEDLINE]
17.

Keratosis pilaris and hereditary koilonychia without monilethrix.

Thai KE, Sinclair RD.

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

PMID:
11568761
[PubMed - indexed for MEDLINE]
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.

PMID:
15744029
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

More than one gene involved in monilethrix: intracellular but also extracellular players.

Schweizer J.

J Invest Dermatol. 2006 Jun;126(6):1216-9.

PMID:
16702971
[PubMed - indexed for MEDLINE]
Free Article
20.

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.

PMID:
21188018
[PubMed]
Free PMC Article

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